Research Assoc Resume Samples

4.5 (81 votes) for Research Assoc Resume Samples

The Guide To Resume Tailoring

Guide the recruiter to the conclusion that you are the best candidate for the research assoc 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
PK
P Klocko
Princess
Klocko
3038 Giles Common
Detroit
MI
+1 (555) 140 8007
3038 Giles Common
Detroit
MI
Phone
p +1 (555) 140 8007
Experience Experience
Chicago, IL
Research Assoc
Chicago, IL
Corwin-Will
Chicago, IL
Research Assoc
  • Propose, design, and lead process improvements using cross-functional and industry network to drive improvements to Lilly QC practices
  • 7) Perform equipment maintenance and calibrations and ensure working area is maintained in a 5S state
  • Assist in composing/developing applications for grants/contracts for funding of research projects
  • 2) Work independently or with other Technical Services personnel to execute experiments
  • 7) Develop new or improved techniques and procedures around specific tasks with minimal supervision
  • 9) Work independently or with other PDTS personnel to execute experiments
  • Assists faculty in the conduct of research of significant value in the basic and/or translational science area
Dallas, TX
Clinical Research Assoc
Dallas, TX
Pfeffer Inc
Dallas, TX
Clinical Research Assoc
  • Supplying sites with study binders and assisting study team in developing source worksheets
  • Manage assigned study sites and networks conducting phase I-IV protocols according to the monitoring plan including source document verification
  • Assists with review and completion of study standard operating procedures and work instructions
  • Works closely with management to review and get approval of clinical trial agreements and site specific budgets
  • Manage data query resolution process with sites and track status updates (i.e. IWS)
  • Assists in ordering, distributing and receiving investigational product
  • Participate in all clinical study project meetings from inception to close out, providing advice on contract process, status and timelines
present
Detroit, MI
Research Assoc, Data Mgmt
Detroit, MI
Dickens-Simonis
present
Detroit, MI
Research Assoc, Data Mgmt
present
  • Assist in the development of protocol and criteria
  • Works collaboratively with research staff in verifying collected data
  • Develop and/or modify techniques and protocols related to the research design
  • Leads database design and oversees database management
  • Conducts data analysis at predetermined study checkpoints and evaluates study progress and results
  • Formulates research methods and suggests options for improving quality
  • Proficient in SPSS, SAS or STATA
Education Education
Bachelor’s Degree in Public Health
Bachelor’s Degree in Public Health
Boston University
Bachelor’s Degree in Public Health
Skills Skills
  • 3) Research lab experience may include research in GMP/QSR environment, cross-functional teamwork, and independent experimentation in method development and validation
  • 7) Able to work in cold environment; able to lift, push, or pull up to 50 pounds
  • Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
  • 7) Good interpersonal skills, good verbal and written communication skills
  • 7) Able to work in cold environment; able to lift, push, or pull up to 35 pounds
  • 4) Ability to handle multiple tasks concurrently while paying attention to details
  • 10) Able to work in cold environment; able to lift, push, or pull up to 35 pounds
  • Excellent working knowledge of cGMP regulations
  • Excellent teamwork and communication skills
  • Attentive to detail
Create a Resume in Minutes

15 Research Assoc resume templates

1

Research Assoc Resume Examples & Samples

  • 3) Contribute to technical feasibility analysis of complex research and design concepts
  • 4) Evaluate results relative to product requirements, definitions and/or program goals
  • 5) Play a lead role in the evaluation, selection and adaptation of various techniques, which accomplish business objectives such as quality and cycle-time
  • 6) May provide training and supervision to junior members within the discipline. Routinely provide advice and assistance to team members regarding unique problems
  • 7) Devise new approaches to complex problems through adaptations and modifications of standard technical principles. Incorporate new methods and technologies for improving existing or new products/processes
  • 8) Maintain current knowledge of relevant QSRs and other regulatory requirements related to R&D (product development, design and safety) to ensure compliance in all research, data collection and reporting activities
  • 9) Develop budgets and activity schedules of limited scope. In addition to having an in-depth knowledge and understanding of GxP and related regulations and guidance, is able to provide expert insights into such regulations so as to facilitate efficient product registration and/or is an active participant in the generation, review, adoption and interpretation of such regulations
  • 10) Independently plan and execute a series of design and/or technical tasks that may not be well-defined, have multiple variables, and require advanced techniques within negotiated deadlines
  • 1) The position requires relevant laboratory skills, writing skills, and computer skills plus teamwork/interpersonal skills
  • 2) Bachelor's degree in a scientific discipline with at least 5-7 years or MS with at least 3-5 years relevant experience, or equivalent
  • 3) Research lab experience may include research in GMP/QSR environment, cross-functional teamwork, and independent experimentation in method development and validation
2

Research Assoc Resume Examples & Samples

  • Bachelor's degree in a scientific discipline
  • Research lab and/or manufacturing experience in GMP/QSR environment is useful, ideally in the biologics industry
  • The position requires relevant laboratory skills, writing skills, and computer skills plus teamwork/interpersonal skills
3

Research Assoc Resume Examples & Samples

  • 1) Design appropriate experiments to achieve process improvements with minimal supervision
  • 2) Work independently or with other Technical Services personnel to execute experiments
  • 3) Supervise and develop a scientific staff of at least one full time employee and several temporary employees
  • 4) Plan and conduct bench scale and pilot scale experiments
  • 5) Assessment of new technology and application to our existing processes
  • 6) Utilize robust statistical analysis to draw appropriate conclusions from the data
  • 7) Develop new or improved techniques and procedures around specific tasks with minimal supervision
  • 8) Write SOPs and batch records, and develop research outlines for scientific projects
  • 1) Knowledge of protein purification techniques
  • 2) Experience in protein process development
  • 3) Knowledge of analytical tools for analysis of proteins
  • 4) Experience with DOE (design of experiments), six sigma, and lean manufacturing a plus
  • 5) Knowledge of GMPs
  • 6) Good interpersonal skills, good verbal and written communication skills
  • 7) Able to work in cold environment; able to lift, push, or pull up to 50 pounds
  • MS degree and > 4 years related experience
  • PhD and 1 year related experience
4

Research Assoc Resume Examples & Samples

  • Set up tracking tools, assist in develop forms and document procedures
  • Summarizes data for progress reports
  • Responsible for reviewing own work to ensure data quality
  • Bachelor's degree in the healthcare field
5

Research Assoc Resume Examples & Samples

  • 1) Conduct laboratory bench and pilot scale protein purification studies, including sample collection, sample preparation, and sample submission
  • 2) Use sophisticated laboratory instrumentation and computer systems to collect and record data
  • 3) Perform advanced assays requiring precise analytical skills and an understanding of biological and chemical principles
  • 4) Complete all testing and analyses of experimental materials in a timely and appropriate manner
  • 5) Prepare study protocols/final reports, maintain data integrity and ensure compliance with company SOPs, GLP, and cGMP regulations
  • 6) Prepare buffers and solutions
  • 7) Perform equipment maintenance and calibrations and ensure working area is maintained in a 5S state
  • 8) Ensure personal training requirements are met
  • 9) Work independently or with other PDTS personnel to execute experiments
  • 1) Knowledge of protein separation and purification techniques
  • 2) Understanding of plasma fractionation is preferred
  • 4) Ability to handle multiple tasks concurrently while paying attention to details
  • 5) Experience with DOE (design of experiments), six sigma, and lean manufacturing a plus
  • 6) Knowledge of GMPs is a plus
  • 7) Good interpersonal skills, good verbal and written communication skills
  • 8) Solid organizational skills
  • 9) Ability to work independently, and follow specific instruction to accomplish the tasks
  • 10) Able to work in cold environment; able to lift, push, or pull up to 35 pounds
  • Bachelors Degree in a scientific discipline with at least 2-3 years relevant experience, or Masters Degree
6

Research Assoc Resume Examples & Samples

  • Analysis of test articles by appropriate biochemical methods such as: HPLC, UV-Vis, and compendial test methods including pH, osmolality, physical appearance, and particle size analysis
  • Initiating QC responsibilities such as sample coordination, lab equipment maintenance, QC document management, QC inventory control and reconciliation of sample requests/documents as needed
  • Monitoring laboratory equipment for temperature and conformance to specifications and applying acceptable cGMP practices during execution of all work tasks
  • Exhibit strong teamwork skills by sharing knowledge and troubleshooting assistance with coworkers, technical mentoring of less experienced associates
  • Delivery of independent projects by
  • Propose, design, and lead process improvements using cross-functional and industry network to drive improvements to Lilly QC practices
  • Development of new methods for validation and transfer, including assay data review
  • Compiling and analyzing data for documentation of test procedures and preparation of reports/graphs to present to manufacturing leadership
  • Perform document reviews and author new QC lab standard operating procedures (SOPs)
  • BS in a related science (e.g., Chemistry, Biochemistry) with minimum 8 years (e.g. regulated compliance industry, FDA industry), or Masters in related science (e.g. Chemistry, Biochemistry) with minimum 6 years of experience (e.g.regulated compliance industry, FDA industry)
  • Previous HPLC experience (method transfer, method validation, method development)
  • Attentive to detail
  • Good computer skills
  • Ability to work independently and achieve problem resolution with minimal supervision
7

Clinical Research Assoc Resume Examples & Samples

  • Ensure the site Investigator Folder is up to date and mirrors the Novartis TMF. Responsible for collecting regulatory documents from site and filing in the Novartis TMF. Prepare and collect study site documents
  • Responsible for utilizing and updating electronic systems to perform job functions (e.g. Outlook, WinFx, ClinTransfer, IMPACT, IWS, eTMF, webEDI, I.MAN, STARS, Vantage, SSU Database, Investigator Portal, LMS, ESOPs, iLearn, Expense reimbursement, CWT Horizon, Metrixx, Timecard, PMP, multiple eCRF applications). Serve as a reference to other CRAs on electronic systems. May be responsible for assisting with the evaluation, design and implementation of new systems
  • Perform additional roles and functions for GenMed Clinical Operations as assigned such as a trial Lead CRA, systems superuser, or committee member
  • Support the successful implementation of innovative processes and technologies.#LI-TW1
  • Solid medical and business knowledge
  • Three to five years of experience as a CRA. Trial Lead CRA experience desirable
  • Demonstrated ability to coordinate, organize, communicate, and manage site activities, with knowledge of when to escalate issues to management or clinical team
  • Advanced understanding of clinical development, knowledge and experience in international (FDA, EMEA, ICH) and local regulations
8

Research Assoc Resume Examples & Samples

  • Highly organized and self-motivated individual with solid understanding of biopharmaceutical purification process development. Strong multidiscipline problem solving skills, excellent communication skills, attention to detail, and ability to lead and influence cross-functional peers and/or upper management. The individual must also have
  • Hands-on experience of purification process development including chromatography, filtration and analytical assays to monitor processes and product characteristics
  • Knowledge of cGMP manufacturing and familiarity with engineering concepts; Knowledge of cell culture principle and techniques
  • Ability to establish and maintain accurate documentation under appropriate guidelines; Ability to present to peers and management team with a concise and fact-based approach
  • Able to communicate well with other groups, and to provide timely feedback to manufacturing group for continuous improvement
  • Team oriented, shares information and coordinates tasks effectively with others
  • Ability to thrive in a fast-paced environment and to multi-task, with good organizational and time-management skills
  • Must have passion to innovate and drive for solutions, and eagerness to learn and continuously improve
9

Research Assoc Resume Examples & Samples

  • 1) Plan and conduct laboratory bench and pilot scale protein purification studies, including sample collection, sample preparation, and sample submission
  • 10) Assessment of new technology and application to our existing processes
  • 11) Utilize robust statistical analysis to draw appropriate conclusions from the data
  • 12) Write SOPs and batch records, and develop research outlines for scientific projects
10

Research Assoc, Data Mgmt Resume Examples & Samples

  • Leads database design and oversees database management
  • Develop and/or modify techniques and protocols related to the research design
  • Conducts data analysis at predetermined study checkpoints and evaluates study progress and results
  • Formulates research methods and suggests options for improving quality
  • Assist in the development of protocol and criteria
  • Works collaboratively with research staff in verifying collected data
  • Proficient in SPSS, SAS or STATA
  • Preferably has at least 3 years of experience
11

Postdoctoral Research Assoc Resume Examples & Samples

  • Strong skills with Python, including OOP and multi-tasking
  • Familiarity with autonomous vehicles or robots
  • Familiarity with GPU based environment/programming
  • Experience with CUDA, NVIDIA Jetson TX1
  • Hands on experiences with Kalman, Extended Kalman filters, Cascades
  • Hands on experiences with optimization theories and real-world problems
12

Clinical Research Assoc Resume Examples & Samples

  • Responsible for establishing and maintaining Electronic Trial Master filing systems, securing essential documents and monitoring files and databases for accuracy and completeness
  • Responsible to perform clerical functions, maintain office / study supplies and equipment, and scanning and electronic filing
  • Responsible for establishing accounts in billing systems within compliance guidelines and issuing payments to vendors and investigators according to executed agreements
  • Works closely with management to review and get approval of clinical trial agreements and site specific budgets
  • Tracks study status, enrollment, regulatory documentation and site start up status
  • Assists in ordering, distributing and receiving investigational product
  • Assists in user acceptance testing and evaluating new upgrades
  • Assists with the preparation of technical reports, summaries, templates and protocols
  • Supplying sites with study binders and assisting study team in developing source worksheets
  • Distributes updates to study sites
  • Records, compiles and distributes minutes from team meetings
  • Maintains all pertinent study correspondences between the sponsor, study sites and third parties
  • Assists with review and completion of study standard operating procedures and work instructions
  • Coordinate research Investigator, Coordinator and monthly forum meetings and newsletters
13

Clinical Research Assoc Resume Examples & Samples

  • Serves as Clinical Research Coordinator/Assistant on multiple protocols, with multiple PIs depending on complexity study and condition of study patient population not to exceed the number determined safe to conduct as directed by supervisor. Research specific to Pulmonary, Cardiac, and ICU which may involve both in-patient (ICU) and out-patient research. Coordinates daily operations of clinical (human) research studies in Internal Medicine, Pulmonary Critical Care Division, with a major focus on pulmonary related diseases
  • Prepares/submits IRB required documents, including but not limited to, Initial Review, Study Protocol, Informed Consent Forms, Questionnaires, Study Recruitment/advertising material, Investigator Brochure, IND safety reporting, Continuing Reviews, Adverse Events (AE) and Serious Adverse Events (SAE)and other IRB documentation
  • Conducts or participates in the informed consent process including interactions with the IRB and discussions with research participants, including answering any questions related to the study. Obtains appropriate signatures and dates on forms in appropriate places on Informed Consent Form (ICF) & HIPAA form. Assures that amended consent forms are appropriately implemented and signed
  • Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials. Collects documents needed to initiate the study and submit to the sponsor (e.g., FDA Forms 1572, CVs, etc.)
  • Prepares other study materials as requested by the PI. These study materials include, but are not limited to, the informed consent document/form, case report forms (CRFs), enrollment/screening logs, and drug/device accountability logs
  • Reviews and comprehends the research protocol. Screen potential study patients - evaluate protocol defined inclusion and exclusion criteria. Explain research and medical procedures to study patients (and family if needed) in Spanish if necessary. Answer patient questions, re-iterated MD instructions and interpret if necessary
  • Schedule research related patient visits. Assists physician with scheduling of necessary procedures and escorts subjects to procedures in the hospital. Schedules, prepares for, and staffs routine visits from CRAs monitoring research procedures
  • Collects data as required by the protocol. Records research data. Collects necessary information from patient charts (i.e., medications, laboratory, ECG and x-ray reports, and charge sheets) and records data in source documentation
  • Process routine clinical samples (i.e. blood, urine) and label specimens appropriately and assure prompt shipping if to outside laboratory. Submit request for dry ice and ship and label samples. Process routine clinical samples (i.e. blood, urine) and label specimens appropriately and assure prompt shipping if to outside laboratory. Submit request for dry ice and ship and label samples
  • Associate’s degree in a field of study related to the clinical research trial plus one (1) year related experience or a combination of related education and/or experience to equal three (3) years
  • Certified Clinical Research Professional as defined by The Society of Clinical Research Associates or ability to obtain certification as a Clinical Research Professional within two years from date of hire or upon eligibility
  • Bilingual - Spanish/English
  • Excellent organizational skills to independently manage workflow
  • Ability to prioritize quickly and appropriately
  • Familiarity with Microsoft Office Suite
  • Pulmonary and/or critical care or work as a respiratory therapist, clinical research/human subjects research experience involving research of medications in the process of being approved by the FDA by pharmaceutical companies (not animal, basic, or epidemiologic research)
  • Knowledge of good clinical practice, FDA , OHRP, HIPPA, policies. IATA training in shipping biologic specimens
14

Clinical Research Assoc Resume Examples & Samples

  • Position will review and assist in the negotiation of terms and conditions while adhering to all applicable Baxter policies
  • Participate in all clinical study project meetings from inception to close out, providing advice on contract process, status and timelines
  • Partner with Legal, Clinical Project Manager and other functional groups to resolve issues in a timely manner and provide guidance on complex contract situations
  • Manage the Clinical Research Organization (CRO) with respect to contracts
  • Continually seek and suggest innovative and more efficient ways to carry out duties
  • Provide mentorship and training to other Contract Associates as needed
  • Demonstrate and incorporate Baxter competencies in executing responsibilities
  • Ability to maintain effectiveness under changing circumstances and priorities
  • Excellent verbal and written communication, presentation, interpersonal and organizational skills required
  • This position requires a sound knowledge of various computer software and meticulous attention to detail
15

Research Assoc Resume Examples & Samples

  • Assists faculty in the conduct of research of significant value in the basic and/or translational science area
  • Plans, conducts, and manages research projects within the federal and institutional regulations and policies
  • Collaborates with researchers, external agencies and institutions to develop cooperative research initiatives
  • Trains technical staff, students, fellows & physicians in lab procedures
  • Reviews manuscripts for peer-reviewed journals
  • Assist in composing/developing applications for grants/contracts for funding of research projects
  • Promotes free discussion, research progress, and overall morale
  • Responsible for appropriate use of research funds
  • May supervises staff and students
  • Master’s degree, 5-7 years of scientifically relevant experience required
  • Bachelor’s degree 10+ years of scientifically relevant experience required
16

Research Assoc Resume Examples & Samples

  • Plans, conducts research projects within the federal and institutional regulations and policies
  • Trains technical staff, students in lab procedures
  • Assists with the submission of grant applications/contracts and funding of research projects
  • Participates in free discussion, research progress, and overall morale
  • May supervise students
  • Terminal degree (MD, PhD, DVM), 1or more years Post-Doctoral fellowship experience
  • Master’s degree, 3-5 years of scientifically relevant experience required
  • Bachelor’s degree, 7+ years of scientifically relevant experience required
17

Clinical Research Assoc Resume Examples & Samples

  • Position will review and play a key role in negotiation of terms and conditions while adhering to all applicable Baxter policies
  • Manage Clinical Research Organizations (CROs) with respect to contracts
  • BS/BA required and/or minimum 4 years of experience
  • Paralegal and/or legal analyst experience
  • Extensive experience negotiating contract terms and conditions
18

mAb Research Assoc Resume Examples & Samples

  • Broad knowledge and experience in cutting-edge research areas, familiar with various antibody generation technologies
  • Knowledgeable of antibody cloning
  • Well-organized, detail-orientated, and self-motivated
  • Master with minimum of 3 years of monoclonal antibody experiences or equivalent educational degree and experience is required
  • Highly experienced in monoclonal antibody generation, and strong problem-solving skills in all aspects of mAb generation process. Experience in developing antibody pairs for diagnostic/detection kits is highly desired
  • Hands-on experiences of multiple antibody characterization techniques including but not limited to ELISA, Western blotting, IP, IF and Biacore (SPR)
19

Clinical Research Assoc Resume Examples & Samples

  • Responsible for coordinating research activities as defined in research study protocols and PI
  • Responsible for screening potential study patients evaluate protocol defined inclusion and exclusion criteria
  • Responsible for ensuring 100% documentation of ICF/HIPAA and maintain in study binder/files
  • Having two years of experience as a full-time Clinical Research Professional (or 3500 hours part time) during the last five years
  • Experience working with Clinical Trials
20

QC Research Assoc Resume Examples & Samples

  • Bachelor or above degree or above in Biology, Chemistry or related field
  • 5+ years experience as a QC specialist with strong sense of quality in mind
  • Master of the QC skill of WB, ELISA and Bio-Plex
21

Clinical Research Assoc Resume Examples & Samples

  • Two (2) years of direct experience in clinical biomedical and/or behavioral research required
  • (LC: RN-TN) Must possess a current Tennessee State Board of Nursing license if primary residence is Tennessee or a Nurse Licensure Non-Compact state
  • (LC: RN-MISS or RN-AR) Must possess a current State Board of Nursing license in the state of primary residence if the state is a Nurse Licensure Compact state