Scientific Writer Resume Samples

4.6 (70 votes) for Scientific Writer Resume Samples

The Guide To Resume Tailoring

Guide the recruiter to the conclusion that you are the best candidate for the scientific writer job. It’s actually very simple. Tailor your resume by picking relevant responsibilities from the examples below and then add your accomplishments. This way, you can position yourself in the best way to get hired.

Craft your perfect resume by picking job responsibilities written by professional recruiters

Pick from the thousands of curated job responsibilities used by the leading companies

Tailor your resume & cover letter with wording that best fits for each job you apply

Resume Builder

Create a Resume in Minutes with Professional Resume Templates

Resume Builder
CHOOSE THE BEST TEMPLATE - Choose from 15 Leading Templates. No need to think about design details.
USE PRE-WRITTEN BULLET POINTS - Select from thousands of pre-written bullet points.
SAVE YOUR DOCUMENTS IN PDF FILES - Instantly download in PDF format or share a custom link.

Resume Builder

Create a Resume in Minutes with Professional Resume Templates

Create a Resume in Minutes
GB
G Boyer
Garett
Boyer
96599 Roberts Locks
Detroit
MI
+1 (555) 654 1852
96599 Roberts Locks
Detroit
MI
Phone
p +1 (555) 654 1852
Experience Experience
Houston, TX
Scientific Writer
Houston, TX
Johns LLC
Houston, TX
Scientific Writer
  • Follow established editorial voice, including managing journal citations using EndNote or other software
  • Interest in writing for marketing/business purposes
  • Assist in the clinical sequencing reporting process for our Mi-Oncoseq Project
  • Ensuring high quality standards for scientific and technical documents of the multivalent Shigella project in line with GVGH standards
  • Assist PI with grant application scientific writing and progress report development
  • Expertise and knowledge in pre-clinical/translational writing
  • Works with lab teams on reporting and analysis, follows validated or experimental analytical procedures with periodic direct supervision
Houston, TX
Senior Scientific Writer
Houston, TX
O'Keefe Inc
Houston, TX
Senior Scientific Writer
  • Conducting interviews with scientists, doctors and academics and establishing a network of academic
  • 20% Collaborate effectively with relevant stakeholders, intra- and inter-departmental functional representatives and submission teams in coordinating development, review and hand-off of nonclinical/clinical sections of regulatory filings and clinical bioanalytical content to Regulatory Ops/Affair, Clinical Ops/Development/Medical Writing
  • 10% Develop and maintain documents templates and high quality systems for tracking of nonclinical components of regulatory submissions, nonclinical study and nonclinical & clinical bioanalytical reports and related nonclinical/clinical bioanalytical sections/content for global regulatory submissions
  • Producing articles for publication in print and online according to agreed style and keeping to
  • Working closely with the grant principal investigator (PI), takes a lead role in preparation and project management of institutional or multi-investigator proposals in support of JAX investigators. [40% effort]
  • Authors complex clinical study protocols and other related documents according to
  • Leads protocol prototyping sessions including the document flow, logic and consistency for assigned project prototypes; critically reviews project specific model documents, maintains protocol prototypes/shells
present
Los Angeles, CA
Scientific Writer / Senior Scientific Writer
Los Angeles, CA
Schumm, Parisian and Goyette
present
Los Angeles, CA
Scientific Writer / Senior Scientific Writer
present
  • Identify existing alternative methods and technologies for improving existing or new products/processes
  • Update and keep current the PCD Writing Group Sharepoint website
  • Without assistance, make sound technical recommendations regarding projects/matters that are more routine than not
  • Contribute to technical feasibility analysis of complex research and design concepts
  • Abides by GLP, GCP, and all company SOP's pertinent to the position
  • Participate in various task force activities and project meetings related to area(s) of responsibility
  • Provide some analysis/redesign of key experimental procedures
Education Education
Bachelor’s Degree in Life Sciences
Bachelor’s Degree in Life Sciences
University of Virginia
Bachelor’s Degree in Life Sciences
Skills Skills
  • Good knowledge of word processing, spreadsheets, table and graph generation and use of applicable computer software
  • Excellent organizational skills and exceptional attention to detail
  • Good working knowledge of scientific terminology, medical, pharmaceutical and research concepts
  • Ability to work collaboratively, meet deadlines, have attention to details, perform multiple tasks simultaneously and prioritize
  • Working knowledge of applicable computer systems (Windows or mac, Microsoft Office)
  • Strong communication skills
  • Proficiency in Microsoft Word and Excel programs
  • Strong experience with Microsoft Word, Excel, and PowerPoint
  • Excellent interpersonal skills
  • Proficient use of English language
Create a Resume in Minutes

15 Scientific Writer resume templates

1

Senior Scientific Writer Resume Examples & Samples

  • 70% Manage preparation, writing, review of nonclinical/clinical components of regulatory submissions and all nonclinical supporting documentation for which the department is responsible. Ensure timely delivery of high quality, submission-ready submission components that are consistent with relevant regulatory guidances for global submissions (eg, US FDA, EMA, PMDA, ICH)
  • 20% Collaborate effectively with relevant stakeholders, intra- and inter-departmental functional representatives and submission teams in coordinating development, review and hand-off of nonclinical/clinical sections of regulatory filings and clinical bioanalytical content to Regulatory Ops/Affair, Clinical Ops/Development/Medical Writing
  • 10% Develop and maintain documents templates and high quality systems for tracking of nonclinical components of regulatory submissions, nonclinical study and nonclinical & clinical bioanalytical reports and related nonclinical/clinical bioanalytical sections/content for global regulatory submissions
2

Scientific Writer / Editor Resume Examples & Samples

  • Develop website content about genetic and rare diseases in plain language
  • Develop publications, brochures and other print and web materials
  • Contribute to the design and layout of written products for the audiences of interest
  • Provide scientific and technical writing assistance in the development of peer-reviewed manuscripts
  • Edit documents for consistency in style, voice, word usage, grammar, spelling, and punctuation, and checking the format of various documents
  • Remain current in the fields of clinical genetics and rare diseases
  • Master’s degree in communications, English, genetics, public health or related social science field required
  • At least 3 years experience in a professional setting as a scientific/technical writer required
  • Experience supporting the development of peer-reviewed manuscripts, newsletters, and other similar publications required
  • Background working in genetics, public health, social science or similar experience preferred
  • Familiarity with writing for the web is preferred
  • Publications on public health, social science, or related topics preferred
  • Knowledge of 508 Compliance preferred
  • Science Writing Certificate, preferred
  • Demonstrate scientific/technical writing and editing skills, with ability to write for both professional and general audiences
  • Excellent verbal, interpersonal and written communication skills
  • Must be able to work effectively with a diverse workforce
  • Should be able to work quickly, accurately, and collaboratively to meet deadlines
  • Good organizational/problem solving skills are needed
3

Scientific Writer Resume Examples & Samples

  • Work with Clinical Content Manager to create/review/edit print and online marketing clinical collateral or messaging (e.g. eblasts, social media messaging with clinical components)
  • Proofread clinical marketing content (non-clinical marketing content as needed) to ensure consistent language, grammatical accuracy, and proper English
  • Assist with writing/reviewing/editing patient, clinician, corporate blogs as needed
  • Assist with clinical updates impacting all marketing materials, both online and in print, including materials targeting clinicians, patients and the general public
  • Follow established editorial voice, including managing journal citations using EndNote or other software
  • Bachelor’s degree (or higher)
  • 1-3 years relevant work experience
  • Experience in science/medical writing
  • Experience in writing/proofreading copy (online and in print)
  • Interest in writing for marketing/business purposes
  • Excellent organizational skills and exceptional attention to detail
  • Proficiency in Microsoft Word and Excel programs
  • Writing and publishing (any media format)
  • Editing
4

Scientific Writer, Immunopharmacology Resume Examples & Samples

  • Prepare the preclinical sections of documents for regulatory submissions (e.g. IND Module 2, investigator brochures, protocols, and formal study reports,) in collaboration with other iONC scientists, and regulatory and submission teams in accordance to company standards and requirements
  • Familiar the regulatory submission process. Manage the internal regulatory database for uploading, review, editing and approval of documents
  • Prepare, review, and edit study reports and operational documents (e.g. protocols, SOPs)
  • Help iONC upper management draft and edit scientific documents for key presentations
  • Oversee the department publication plan and patent filing and ensure the quality of the publication
  • Participate scientific activities, keep abreast of iONC pipeline projects and contribute to the implementation of the iONC research strategy
  • Ph.D./M.D. with at least 3 years of experience in pharmaceutical industry
  • At least 5 years of research experience in cancer immunotherapy or closely related areas, and comprehensive understanding of in vitro immunological assays, in vivo models, and FACS and biomarker analysis
  • Working knowledge of statistical analysis
  • Proven track record of writing study reports, especially for regulatory submission
  • Demonstrated excellence in scientific writing, especially in the areas of immuno-oncology
  • Strong familiarity with computer writing programs and software
  • Very good oral and written communication skills
  • Demonstrated ability to write scientific reports and publications
  • Team player with strong communication skills
  • Strong organizational skills and attention to details
  • Self-directed; able to adhere to tight timelines
  • Forward-thinking and creative with high ethical standards
5

Associate Scientific Writer Resume Examples & Samples

  • B.S. in chemistry or related science
  • 1-2 years experience in an analytical testing laboratory
  • Excellent grammatical skills and exceptional communication skills, both written and oral to keep others informed of progress and particularly of changes in status of work
  • Possesses good editorial/proofreading skills and understands and performs well the process of writing (outlining, drafting, revising, and reviewing)
  • Excellent organizational skills
  • Proficient with Microsoft Word and Excel
6

Scientific Writer Resume Examples & Samples

  • Manages multiple projects at any given time
  • Comply with and support oncology scientific writing (OSW) group’s project management tool, standards, policies and initiatives
  • Follow Novartis specifications for documentation, specifically Novstyle, templates etc
  • Follow and track clinical trial milestones for assigned projects
  • Maintain records for all assigned projects including Datavision and other databases
  • Contribute to development of processes within OSW group
  • Support development of OSW group through participating in OSW group initiatives and other related activities
  • Builds working relationships and actively collaborates with key internal and external stakeholders to optimize feed-back and input towards high quality documents
  • Performs additional tasks as assigned
  • Participate in international congresses and conferences; development of pre and post congress scientific communication deliverables
7

Senior Scientific Writer Resume Examples & Samples

  • 3-5 years relevant experience
  • Communication skills, both written and oral
  • Detail-oriented and able to follow timelines
  • Possesses good editorial/proofreading
  • Outline, draft, revise, and review
  • Working knowledge of complex analytical laboratory procedures
  • Problem solving skills
8

Senior Scientific Writer Resume Examples & Samples

  • Consults with faculty at both JAX campuses (Farmington, CT, and Bar Harbor, ME) and with collaborating institutions on individual grant and award preparation, providing advice on scientific writing and grantsmanship, as well as editorial support and standardized language for administrative portions of basic, translational and clinical grant applications. [30% effort]
  • Working closely with the grant principal investigator (PI), takes a lead role in preparation and project management of institutional or multi-investigator proposals in support of JAX investigators. [40% effort]
  • Exceptional written communication skills to prepare and edit competitive grant proposals, publications, administrative materials, other research communications and clinical protocols
  • Exceptional interpersonal skills to build teams and trust among known and unfamiliar professionals in a high-pressure environment. Must possess the ability to interact positively and professionally with very senior faculty and leadership
  • Excellent organizational skills to manage the project management and writing process (draft preparation, review and revision) of complex grant proposals and deliver fundable proposals in a timely manner to meet both interim and final deadlines
  • Ability to grasp complicated technical subjects, synthesize diverse lines of evidence and apply these abilities to technical writing
  • Ph.D. in physical or natural sciences with extensive and sustained grant writing experience (5+ years)
  • M.S. in physical or natural sciences or a professional degree may also qualify, depending on background, training and experience
9

Scientific Writer Intern Resume Examples & Samples

  • Must be rising junior in a Bachelors program or above (preferred PhD), with a minimum 3.2 GPA – both cumulative and major (will be verified by transcripts)
  • Must have strong communication skills and ability to work effectively in a collaborative environment
  • Preferred Course of Study: Molecular biology
  • Required: Has drafted (with or without supervision) at least one scientific publication and/or conference materials (abstracts, posters, slide decks)
  • Preferred: Expertise with Microsoft Word, Excel, PowerPoint, and reference software; knowledge of biological statistical methods
10

Scientific Writer Resume Examples & Samples

  • Leads scientific writing, research, and department projects efficiently and timely
  • Communicates on-going project status, potential issues, and timelines to Chairman, Medical Director and/or Principal investigator(s)
  • Plans, organizes, and manages all aspects of assigned retrospective, outcome and prospective projects and key deliverables
  • Leads and manages the efforts of all key cross-functional departments to perform all project� related activities according to project milestones/timelines in a manner consistent with the stated project timelines and ethical transparent business practice
  • Discusses the cultivation of any identified opportunities or roadblocks to the successful completion of the project
  • Performs scientific investigation of content to support grants, journal activities, and other materials related to the support of the department
  • Prepares meeting agendas/content to support Chairman, Medical Director
  • Manages reference/bibliography records
  • In collaboration with Chairman, Medical Director, and other Department leadership, develops content for Department webiste, quarterly newsletter and other materials representing department activities/accomplishments
  • Performs other duties as assigned by the Chairman at LCI and other CHS sites
11

Scientific Writer Resume Examples & Samples

  • Good working knowledge of the organization’s service offerings and processes
  • Develop high-quality scientific content by means of all necessary research, scientific writing, editing, and fact checking, to meet deadlines and work within project scope and objectives. Applies to all formats of MedCom’s communication outputs
  • Acquire and maintain effective understanding of relevant therapy areas, client products, and objectives
  • Take ownership of assigned projects and resolve basic technical issues to ensure excellent project delivery. Liaise effectively with client and external authors/opinion leaders during the lifecycle of assigned projects
  • Proficient use of English language
  • Work experience not essential
12

Associate Scientific Writer Resume Examples & Samples

  • 1+ year of Clinical, Writing, Publishing and/or Pharmaceutical experience
  • Working knowledge of relevant FDA pharmaceutical promotional guidelines in order to ensure agency output is compliant
  • Solid analytical and research skills
  • PharmD, PhD in Life Sciences, or MD
  • Experience in Medical Advertising and/or Communication, Marketing / Strategic Planning, and the Journal Publication process
  • Prior experience with Medical Devices, Ready-to-use Injectable, and/or Surgical or Anesthesia knowledge
13

Senior Scientific Writer Resume Examples & Samples

  • Prepares manuscripts, literature review, abstracts, posters, and slide sets working from various data sources including clinical study reports, patient profiles, protocols etc
  • Performs quality control (QC) checking / proof reading of literature review, abstracts, posters, and slide sets to meet customer expectations
  • You have to lead up to two assigned team projects at any given time
  • Ensures getting feedback from customers and supports implementation of customer management tactics
  • Comply and support group’s project management tool, standards, policies and initiatives
  • Follow Novartis specifications for documentation, specifically Novstyle, templates etc.. and track the clinical trial milestones for assigned projects
  • Maintain records for all assigned projects including archiving
  • To maintain audit, SOP and training compliance
  • Have to perform additional tasks as assigned
14

Expert Scientific Writer Resume Examples & Samples

  • Demonstrate a command of assigned therapeutic areas and expertise with assigned products
  • Research and write original content for publications activities (primary and review manuscripts, abstracts, posters), slide presentations and other materials
  • Research, develop and write content that is scientifically accurate, evidence-based, grammatically accurate, referenced using appropriate sources, and consistent with quality standards
  • Clearly communicate medical scientific concepts in a condensed, audience-appropriate way
  • Demonstrate the flexibility/adaptability necessary to function on different therapeutic teams as needed
  • Interpret and apply clinical data in medical communication deliverables
15

Senior Scientific Writer Resume Examples & Samples

  • Coordinates the authoring of high-quality clinical study protocols and other related clinical/regulatory documents (e.g., protocol amendments, revised protocols, administrative letters) across multiple phases of development
  • Ensures that all assigned documents support the development strategy to achieve team objectives and timely submission in key geographies
  • Participates in relevant sub-team(s) of the development team and ensures effective planning and management of timelines for all components of assigned documents
  • Leads protocol prototyping sessions including the document flow, logic and consistency for assigned project prototypes; critically reviews project specific model documents, maintains protocol prototypes/shells
  • Authors complex clinical study protocols and other related documents according to
  • PhD/MD/PharmD in a relevant scientific discipline with a minimum of 1-2 yrs of post‑doctoral training, or MS / BS with a minimum of 2 years (MS) to 5 years (BS) of experience in regulatory documentation (preferably in clinical development) or equivalent
  • At least 3 years of scientific writing experience in preparing clinical, regulatory, and/or registrational documents. AMWA (American Medical Writer’s Association) and/or BELS (Board of Editors in the Life Sciences) certification(s) desirable
  • Demonstrated strong writing skills as evidenced by good quality writing in publications in peer-reviewed journals or in pharmaceutical regulatory documentation
  • Analyzed and interpreted complex data from a broad range of scientific disciplines
  • Demonstrated ability to work in a cross-functional project team; manage timelines and track deliverables using strong organizational, communication, facilitation and interpersonal skills; proactively identify risks and propose mitigation strategies; facilitate discussions and timely decision-making between authoring and development team members
  • Familiarity with FDA, ICH, and GCP guidelines for clinical research and data reporting
16

Scientific Writer Resume Examples & Samples

  • 3-5 years experience in technically related field or previous scientific writing experience
  • Ensuring high quality standards for scientific and technical documents of the multivalent Shigella project in line with GVGH standards
  • Generate or support generation of scientific and technical project documents/presentations with oversight from the multivalent Shigella project leader and Head of Project Portfolio, and in collaboration with subject matter experts of the project team (eg, technical development, immunoassay unit, clinical development and regulatory affairs, and project management)
  • Maintain project specific databases and spreadsheet
  • Maintain repository of project relevant literature, including patents and regulatory guidelines, and reference manager database
  • Support generation of quality and preclinical sections of the Investigational New Drug Applications
  • Follow established Health, Safety and Environment policies. Actively participate in training, hazard identification and other HS&E programs. Stop the activity or operation if it is unsafe or is out of compliance and report it immediately to management
17

Scientific Writer, Aggregate Reports Resume Examples & Samples

  • Coordinate and author documents needed for regulatory submissions (eg, CSRs, CTD summary documents, aggregate safety reports, risk management plans), ensuring the coordination and integration of the scientific, medical, and regulatory input from cross-functional team members
  • Participate in relevant document sub team(s) and ensure effective planning and management of timelines for all components of assigned documents
  • Participate in document strategy sessions, including messaging, document flow, logic, and consistency for assigned projects
  • Comply with internal and external processes and guidelines while managing the review process and, on an ongoing basis, resolve issues, errors, or inconsistencies with pertinent team members to ensure timely completion and high quality of assigned documents
  • Review and edit documents as required
  • Considerable experience in Assignment on Cross Functional Teams would be an advantage
18

Senior Clinical Scientific Writer Resume Examples & Samples

  • University degree (PhD preferred) in Medicine, Pharmacology, Biology or related scientific discipline
  • At least five years of experience in scientific/medical writing with a pharmaceutical or biotechnology company; a contract research organization; or at least seven years of relevant professional experience in a related field
  • Knowledge and understanding of International Conference on Harmonisation and Food Drug Administration guidelines pertaining to reports, publications and marketing materials
  • Expertise in analytical evaluation of scientific data, organizational skills, and the ability to work in a team environment
  • Knowledge of product areas, current developments, and keeping abreast of current literature
  • Word processing software (MS Word) proficiency and meticulous attention to detail
  • German is a benefit
19

Scientific Writer Resume Examples & Samples

  • Prepares literature review, abstracts, posters, and slide sets working from various data sources including clinical study reports, patient profiles etc
  • Performs quality control (QC) checking / proof reading of above documents to meet customer expectation
  • Manages assigned individual projects
  • Obtains feedback from customers
  • Complies with and support group’s project management tool, standards, policies and initiatives
  • He / She should follow Novartis specifications for documentation, specifically Novstyle, templates etc
  • He / She should follow and track clinical trial milestones for assigned projects
  • Maintains records for all assigned projects including archiving
  • Maintains audit, SOP and training compliance
20

Scientific Writer Resume Examples & Samples

  • Prepares and/or assists in the preparation of scientific documents such as methods, protocols, reports, method development summaries, analytical methods, SOPs, client correspondence and other similar documentation
  • Compiles laboratory data into a specified report format. Ensures that hardcopy and electronic reports are consistent and comply with required formats. Reviews data tables and listings and ensures that errors are corrected. Performs a quality control review of scientific documents prior to creation of the final pdf deliverable. Ensures compliance with PPD, Client, eCTD policy and procedure on publications
  • Reviews scientific documents for accuracy, formatting, consistency and compliance to protocols or SOPs
  • Works with senior staff to determine approach for new assignments
  • Keeps updated on the guidelines and requirements of the FDA and other international regulatory agencies for reference in the development of required documents
  • Good working knowledge of scientific terminology, medical, pharmaceutical and research concepts
  • Working knowledge of industry regulations, ICH or other regulated environements
  • Working knowledge of analytical laboratory procedures
  • Ability to work well in a collaborative team environment
21

Scientific Writer Resume Examples & Samples

  • Minimum bachelor’s degree with an emphasis in writing and a scientific discipline (biology, chemistry, nutrition, etc.) or equivalent experience
  • Strong knowledge of needed writing skills
  • Working knowledge of applicable computer systems (Windows or mac, Microsoft Office)
22

Scientific Writer / Senior Scientific Writer Resume Examples & Samples

  • Provides editorial support, ensuring quality of all scientific content, with a focus on clarity, accuracy and consistency, while maintaing adherence to proper format, regulatory requirements, and company guidelines/styles/drafting processes
  • Initiates and manages multiple rounds of document review and ensuing revisions, interacting positively and professionally with all levels of reviewers, effectively resolving conflicts and building consensus at every step in the revision process, while ensuring accuracy, consistency and quality of the final document
  • Critically reviews, interprets and conceptually organizes results from complex submission-supporting study reports, deriving clear, concise and scientifically accurate key messages that support regulatory submission strategies
  • Represents the Scientific Writing group on multi-disciplinary drug development teams, proactively identifying and promptly communicating to management any potential obstacles or issues impeding timely completion of deliverables
  • May assign work to, and oversee the activities of, the Associate Scientific Writers
  • Participate in various task force activities and project meetings related to area(s) of responsibility
  • Update and keep current the PCD Writing Group Sharepoint website
  • Abides by GLP, GCP, and all company SOP's pertinent to the position
  • Exceptional interpersonal skills for dealing positively and professionally with senior SMEs and reviewers at all levels within the company
  • Proficient in the use of electronic data bases for document drafting (e.g., SharePoint, Documentum, etc.) and electronic document review software (e.g., PleaseReview)
  • Prepares all documents with scrupulous and unfaltering attention to detail, performing all necessary crosschecks to ensure accuracy of reported data
  • Ability to grasp complicated technical subjects, synthesize diverse lines of evidence and apply these abilities to scientific writing
  • Thorough understanding of the drug development process
  • Comfortable working with incomplete information in a fast-paced, continually changing and rapidly evolving environment
  • Works effectively on multi-disciplinary teams, using strong organizational, communication, and interpersonal skills to faciltate discussions and decision-making
  • Communicates clearly, effectively and in a timely manner to many levels within the company
  • Flexible, with a positive attitude and a demonstrated ability to manage multiple competing priorities under time constraints, while ensuring consistent, high quality of all deliverables
  • Approaches assignments with an entrepreneurial spirit, regularly seeking opportunities to contribute added value; proactively contributes to continuous improvement in the Scientific Writing group
  • Able to work effectively in a flexible environment, including distance-based working relationships
  • Fluency in the English language is required
  • Awareness of compliance issues and guidelines germane to IND and BLA submissions
23

Scientific Writer / Senior Scientific Writer Resume Examples & Samples

  • Without assistance, make sound technical recommendations regarding projects/matters that are more routine than not
  • Provide some analysis/redesign of key experimental procedures
  • Independently select techniques and procedures to solve problems within area of responsibility
  • Employ appropriate techniques/methods to successfully and independently execute routine assignments within negotiated deadlines
  • Identify existing alternative methods and technologies for improving existing or new products/processes
  • Maintain knowledge of relevant QSR and safety requirements while building knowledge of other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities
  • Recommend appropriate designs, techniques and processes for a specified sequence of tasks where needed
  • Contribute to technical feasibility analysis of complex research and design concepts
  • Apply technical theories and principles to projects within area of expertise for non-routine tasks
  • Analyze and determine best solutions to non-routine experimental design or research problems with minimal assistance
  • Accurately assess results for validity and conformance to specifications
  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’) or equivalent combination of education, training, & experience
  • List knowledge, skills, and/or abilities
  • Analytical chemistry or elemental impurities experience a plus but not required
  • Knowledge/application of stoichiometry
  • Technical writing and review experience
  • Ability to demonstrates the relevant laboratory/technical, writing, and computer skills
  • Ability to demonstrate flexibility and can shift gears comfortably
  • Ability to objectively assess, organize, and clearly communicate complex information
  • Interpret available information and make recommendations to resolve technical challenges
  • Appropriately prioritize assignments to meet project schedules
  • Good knowledge of word processing, spreadsheets, table and graph generation and use of applicable computer software
  • Working knowledge of industry regulations, ICH, GxP, or other regulated environements
  • Good editorial and proofreading skills
  • Good problem solving and troubleshooting abilities
24

Scientific Writer Resume Examples & Samples

  • Possesses a thorough understanding of laboratory procedures and can reliably conduct complex analysis with increased independence
  • Works with lab teams on reporting and analysis, follows validated or experimental analytical procedures with periodic direct supervision
  • Responsible for review and compilation of results and data comparison against SOP acceptance criteria, methodology, protocol and product specifications
  • Enters data into databases and reports
  • Performs self review for own data prior to QC submission
  • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years’) or equivalent combination of education, training, & experience. OR Masters degree
  • Experience with writing and reviewing laboratory reports and documents. Experience with data analysis and review as well as compilation. Demonstrated knowledge of multiple applicable techniques such as: bioanalytical techniques, ELISA, immunoassays, bioassays or similar
  • Proficient in Microsoft Excel and Word
  • Proven ability to interpret data by performing trend analysis
  • Proven ability in technical writing skills
  • Ability to independently optimize analytical methods
  • Proven problem solving and troubleshooting abilities
  • Good written and oral communication skills
  • Time management and project management skills
  • Ability to work in a collaborative work environment with a team
25

Scientific Writer Resume Examples & Samples

  • Write and/or edit scientific content for grant proposals, reports, correspondence, articles and presentations. This will include figure development and editing of manuscripts by other lab members
  • Assist PI with grant application scientific writing and progress report development
  • Assist in the clinical sequencing reporting process for our Mi-Oncoseq Project
26

Scientific Writer Resume Examples & Samples

  • High level of proficiency with Microsoft Word; proficient with Microsoft Excel and Power Point and with Adobe Acrobat
  • Demonstrated ability to write, edit, and proofread medical and scientific documents
  • General familiarity with how research with human subjects is regulated
  • Demonstrated problem-solving and interpersonal skills that facilitate effective interactions within cross-functional teams and with external customers
  • Ability to identify issues and generate solutions or request appropriate intervention by management
  • Excellent organizational, communication, and interpersonal skills, both oral and written
  • Basic understanding of medical and scientific terminology, especially as it relates to biomedical basic and clinical research
  • Proven ability to work in a fast paced, demanding environment and adapt to changing priorities without supervision
  • Bachelor’s degree in a science or health profession
  • Certification in clinical research administration (or eligibility for certification within six months) or AMWA Essential Skills certificate within twelve months
  • At least two years of experience with technical, scientific, or medical writing in an academic medical environment, a pharmaceutical environment, a biotechnology company environment, or the equivalent (this requirement may be satisfied by experience in a relevant advanced degree program or post-doctoral position)
  • At least two years of experience in analyzing data, interpreting information, and providing logical conclusions
  • Advanced degree in a science or health profession
  • Oncology experience
  • Proficient with reference management software (EndNote preferred)
27

Scientific Writer Resume Examples & Samples

  • Collaborate with translational scientists and appropriate representatives from various scientific disciplines (Pharmacology, Toxicology, Drug Metabolism & Pharmacokinetics) for compiling and writing pre-clinical and translational manuscripts and other scientific documents such as study reports, pre-clinical and translational sections for regulatory submission dossier
  • As needed, review work of other writers for accuracy, quality, focus, and adherence to format and stylistic requirements in order to ensure high quality documents
  • Advanced degree in biological or related sciences (MS or PhD)
  • Excellent scientific writing and verbal communication skills. Demonstrated ability to compile concise summaries of complicated data sets
  • Expertise and knowledge in pre-clinical/translational writing
  • More than 5 years of previous experience in independently authoring scientific publications, reports, and/or review articles, preferably in pharmaceutical related fields
  • Advanced skills in use of Microsoft Word, Excel, data graphics software, Adobe Acrobat, and web-based browser software such as LiveLink to manage electronic document authoring, reviewing, and approval process
  • Knowledgeable in pre-clinical development and translational sciences
  • Advance knowledge of document guidelines for regulatory submission to FDA and other global regulatory bodies
28

Expert Scientific Writer Resume Examples & Samples

  • Work in conjunction with account management and manager to develop and adhere to logical and attainable timelines for project completion
  • Provide input and aid in troubleshooting/problem-solving
  • Collate and incorporate author/customers comments
  • Lead and/or participate in author/client teleconferences and answer content-related questions
  • Provide accurate citations in text (utilizing Reference Manager system), a bibliography, and appropriately annotated references for medical review
  • Review/revise other writers documents (eg. India)
  • Participate in strategic publications planning and related research
  • Work as part of a team to ensure that it is meeting company goals and objectives, and adhering to corporate values
  • Represent the organization in an appropriate manner
29

Scientific Writer Resume Examples & Samples

  • Write, edit (content, style and grammar/spelling), and proofread­ R01 and R01-like grant proposals, scientific manuscripts for peer review, INDs, clinical and IRB protocols, or other scientific documents for faculty, research fellows, and students
  • Assist with maintenance of databases and/or reference libraries
  • Search the internet and other sources for foundation and government grant opportunities
  • Translate scientific abstracts into lay terms
  • Assist with planning and conducting educational courses and workshops
  • Assist with assembling scientific documents as necessary (e.g., large institutional grants, annual/occasional reports, progress reports for grants admin., IND applications, etc.)
  • Assist Graduate School in assembling, editing, and publishing the Graduate School catalog, and other promotional materials, etc
  • Assist with maintenance/update of department website
  • Master’s degree and one or more years scientific writing experience, preferably in a healthcare/research/academic environment
  • Experience writing grants, including NIH R01 proposals, and/or experience with IND applications and clinical protocols preferred
  • Education in Biology, biochemistry, or other life science is preferred
  • Excellent interpersonal skills
  • Competence with on-line searches
  • Ability to work collaboratively, meet deadlines, have attention to details, perform multiple tasks simultaneously and prioritize
  • Strong experience with Microsoft Word, Excel, and PowerPoint
  • Knowledge of Adobe Acrobat, PhotoShop
  • Knowledge of Data analysis/graphing software, Adobe Illustrator, and database software is preferred
  • Understanding of HTML an asset
30

Scientific Writer Resume Examples & Samples

  • Writes, reviews, edits (content, logic, style, and grammar/spelling), and proofreads­ R01 and R01-like grant proposals, scientific manuscripts for peer review, or other scientific documents for faculty, research fellows, and students
  • Works to increase the number of grant submissions, especially to federal funding agencies
  • Works independently and with others to identify new grant opportunities on behalf of City of Hope investigators
  • Assists with planning and conducting educational courses and workshops on grantsmanship and scientific writing
  • Collaborates on the maintenance of databases and/or reference libraries related to grant funding opportunities
  • Assists Manager with various projects involving scientific documents (e.g., complex institutional grants, annual/occasional reports, progress reports for grants, templates and institutional text for non-techinical components of research proposals)
  • Requires a PhD in biology, biochemistry, or other life science or a masters degree with at least three years of scientific writing experience in a healthcare/research/academic environment
  • Experience in developing and writing research grants, and in reading and interpreting funding opportunities
  • Requires excellent organizational and interpersonal skills, attention to detail, and customer service skills
  • Ability to work independently and as part of a team, meet deadlines, perform and prioritize multiple simultaneous tasks
  • Requires judgment that that could affect image of City of Hope
  • Strong written and verbal communication skills are required
  • Must be able to communicate effectively with diverse audiences
  • Subject to irregular hours and changing priorities; candidate must be able to handle stressful conditions whilst maintaining a high quality of workmanship
31

Scientific Writer Resume Examples & Samples

  • 75% Develop and submit large, multidisciplinary, and multi-collaborative grant proposals to a wide range of funding agencies and organizations, including both public and private external entities. Assist with assembling scientific documents as necessary (e.g., large institutional grants, annual/occasional reports, progress reports for grants admin., IND applications, etc.)
  • 15% Search the internet and other sources for foundation and government grant opportunities. Translate scientific abstracts into lay terms
  • 10% Performs other related duties as assigned or requested such as presentation of draft ideas and plan to investigators, coordination of meetings required to create collaborative interactions both within and outside City of Hope, and reporting of progress to Principal Investigators
  • Communication - Expresses ideas clearly and constructively (written and spoken, upward and downward, one-on-one and with groups)
  • Customer Service - Seeks to understand customer needs and works to exceed customer expectations (internal and external)
  • Initiative - Looks for opportunities to improve performance; manages time, work, and relationships effectively and efficiently
  • Professionalism - Treats others with respect; abides by the institutional values; displays a positive and cooperative attitude; adheres to the workplace Code of Conduct and compliance policies
  • Stewardship - Identifies efficiencies to reduce redundancy and/or elimination of tasks resulting in savings of cost, resources, and or/time
  • Teamwork - Works proactively and collaboratively with others to streamline work and achieve mutual goals
32

Scientific Writer Resume Examples & Samples

  • Advanced/terminal degree in a science or health profession strongly preferred
  • Experience in an NCI-designated Cancer Center and working knowledge of Cancer Center Support Grant (CCSG) administrative guidelines, activities and responsibilities essential
  • Significant experience in an academic medical environment, working in research involved with technical/scientific writing
  • Grant writing experience and scientific manuscript preparation and submission experience
  • Understanding of scientific methodology
  • Excellent organizational and planning skills; leadership ability to manage multiple projects and work assignments with competing deadlines
  • Ability to prioritize, focus, work independently, and be flexible when contingencies arise. Ability to identify issues and generate solutions, or request appropriate intervention by management
  • High level of proficiency in Adobe, MS Word, Excel, PowerPoint, and various databases required. Experience with various graphic and presentation software a plus
  • Demonstrated experience analyzing data, interpreting information, provide logical conclusions/projections and program evaluation and anticipating costs/obligations
  • Ability to work in and appreciate a culturally diverse organization
  • Significant experience in project management, time management and organizational skills, with the ability to manage details of multiple and complex projects with firm schedules and competing deadlines. Proven ability to work in a fast-paced deadline-driven work atmosphere and able to assess environment and adjust plans according to situation with a solution-oriented perspective
  • Advanced understanding of medical and scientific terminology
  • Proven ability to work in a fast paced, demanding environment, and adapt to changing priorities without supervision
  • Considerable experience in analyzing data, interpreting information, providing logical conclusions
  • Program/project management experience
  • Ability to develop and implement innovative and creative approaches to seminal events
  • Demonstrated integrity, dependability, sound judgment, teamwork and resourcefulness to establish and maintain collaborative, positive and effective working relationships with multiple internal and external partners on behalf of UFHCC leadership
33

Senior Scientific Writer Resume Examples & Samples

  • Producing articles for publication in print and online according to agreed style and keeping to
  • Excellent scientific writing skills
  • A strong interest and background in science writing for expert and lay audiences
  • Ability to think logically and understand complex scientific concepts and data
  • Ability to work under pressure to deadline
34

Scientific Writer / Editor Resume Examples & Samples

  • Ability to research and synthesize information in both written and oral form
  • Ability to work independently and effectively under general supervision
  • Excellent time management and attention to detail
  • Ability to communicate and collaborate with diverse audiences and stakeholders
  • Initiative and creativity on the job along with the ability to problem solve
  • Superior listening skills to uncover information needs
  • Previous experience working in the publishing industry