Clinical Research Physician Resume Samples

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NB
N Brakus
Nicholaus
Brakus
58166 Torp Lakes
Boston
MA
+1 (555) 460 1216
58166 Torp Lakes
Boston
MA
Phone
p +1 (555) 460 1216
Experience Experience
New York, NY
Clinical Research Physician
New York, NY
Goyette LLC
New York, NY
Clinical Research Physician
  • Assist Operations and Client Managers with sponsor visits
  • Provides responsible, competent medical research advice to management
  • Perform on-study and post-study physical examinations to ensure that the physical and mental wellbeing of volunteers is undiminished at the end of the study
  • Provides leadership to the clinical study team involved in the execution of clinical studies
  • Review and evaluate protocols and provide clinical and scientific support
  • Provide all necessary medical support functions as defined by project specific contractual obligations which will include, but not be limited to, the following
  • Participate in the on-call system for providing 24/7 medical support
Dallas, TX
Clinical Research Physician Neuroscience
Dallas, TX
Cronin Group
Dallas, TX
Clinical Research Physician Neuroscience
  • Perform local AE review and provide general medical support for safety issues
  • Provide assistance to ICRO and site for IEC/IRB Interactions
  • Provide medical expertise support to pharmacovigilance activities
  • When necessary, provide medical expertise to Clinical Operations activities for safety amendments, INs, etc
  • Assist in writing country or site specific Informed Consent Forms (ICF)
  • May be called upon to provide strategic medical input into protocol design at a global level
  • Lead and/or perform protocol, country and site feasibility
present
Detroit, MI
Medical Director, Clinical Research Physician
Detroit, MI
Lesch, Greenholt and Frami
present
Detroit, MI
Medical Director, Clinical Research Physician
present
  • Participates in Development Strategy to make recommendations, take action and provide clinical research expertise
  • Prepare, present and manage materials for external advisory boards to guide protocol and product development
  • Interact seamlessly with biomarker translational scientists to inform and refine clinical product development and strategy
  • Engage and inspire the project/clinical development team through communicating the strategic vision and the operational plan to achieve the vision
  • Provides high quality, current and timely medical/scientific input into sections of key documents relevant (IB, annual safety reports, etc) to the area of responsibility
  • Provides medical, clinical and scientific guidance to the study team, affiliate medical personnel and investigative sites
  • Provide clinical leadership to allow for initiation of trials in EU in collaboration with regulatory and clinical operations team members
Education Education
Bachelor’s Degree in Clinical Medicine
Bachelor’s Degree in Clinical Medicine
Johnson & Wales University
Bachelor’s Degree in Clinical Medicine
Skills Skills
  • Knowledgeable in the areas of clinical research and regulatory affairs as they relate to clinical studies and healthcare management
  • Intermediate knowledge of Microsoft Word 2013, including the ability to troubleshoot issues
  • Previous research experience – basic and/or translation is desirable
  • Able to demonstrate strong communication, interpersonal, organizational, and negotiating skills
  • Excellent teamwork skills
  • Ability to influence others (both cross-functionally and within the function) in order to create a positive working environment
  • Demonstrated ability to influence others (both cross-functionally and within the function) in order to create a positive working environment
  • Demonstrated strong communication,, interpersonal, teamwork, organizational and negotiation skills
  • Demonstrated ability to balance scientific priorities with business priorities
  • Regulatory experience in support of INDs, BLAs, NDAs, supplemental applications etc. is desirable
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12 Clinical Research Physician resume templates

1

Clinical Research Physician Resume Examples & Samples

  • Participate in executing a clinical protocol for a phase III clinical trial comparing two smallpox vaccines, including but not limited to conducting medical histories and physical examinations, assessing clinical laboratory tests, wet reading of EKGs, assessing cardiac risk, calculating renal clearance, calculating BMI, administering vaccine, assessing adverse events and evaluating data related to the immune response and trial outcomes
  • Prepare or assist in the preparation of reports of research activities and results/outcomes for submission to the Food and Drug Administration (FDA) and assist with preparing manuscripts of research activities and results/outcomes for publication as assigned by Lead Principal Investigator and Site Principal Investigator
  • Participate in meetings and presentations related to assigned duties and/or work performed
  • As required, trains and assists coworkers and technical staff in special knowledge and skills
  • Provide any required written summaries, reports, and other documents as needed in support of the clinical trial
  • The contractor shall perform duties and responsibilities independently based on broad guidelines and objectives provided by the Lead and Site Principal Investigators and own initiative. Performance is evaluated based on the completeness, accuracy and timeliness of results, conformance to established policies, standards and objectives, and, effectiveness of communications and interpersonal skills
  • Provide administrative and logistics support of trial as needed
2

Clinical Research Physician Neuroscience Resume Examples & Samples

  • Lead and/or perform protocol, country and site feasibility
  • Provide protocol, Risk management plan & disease training as appropriate at Investigator’s Meetings or scientific venues or internally
  • Provide medical expertise support to pharmacovigilance activities
  • Follow-up with the Investigator for additional information or clarifications as needed
  • When necessary, provide medical expertise to Clinical Operations activities for safety amendments, INs, etc
  • Review and try to resolve local medical issues / questions that arise during the entire course of the study
  • Assist in writing country or site specific Informed Consent Forms (ICF)
  • May be called upon to provide strategic medical input into protocol design at a global level
  • Support planning, implementation and follow-up of regulatory agency inspections and internal audits
  • Ability to assess the feasibility of implementing the protocol based on regional medical practice
3

Clinical Research Physician Resume Examples & Samples

  • As Clinical Research Physician/Scientist you are responsible for planning, preparation, conduct and reporting of Phase II - IV clinical trials mainly in the areas of cardio-metabolism and/or CNS within the department of Clinical Research Germany
  • As local study manager, you are the leader of the local trial team being responsible for the local performance, quality and oversight in multinational clinical trials. This includes selection of investigational sites, development of key documents for the local regulatory submission, and performance of investigational sites regarding quality and recruitment. You are the local point of contact for medical and operational questions of investigational sites and of your trial team. Furthermore you are responsible for the local trial budget
  • As international study manager, you are the leader of the international trial team being responsible for the global performance, quality and oversight in multinational clinical trials. As author of the Clinical Trial Protocol, you are in close contact to relevant stakeholders in the clinical development and translational medicine organization. You are in contact with external experts and external partners required for conduct of the clinical trial. Organization of trial-specific meetings, e.g. Investigator´s Meeting, Data Monitoring Committees is within your expertise. You are the main contact person for medical and operational questions of the investigational sites and of the trial team. Furthermore you are responsible for the global budget of the trial including external partners
  • You ensure adherence to local and international, internal and external regulations, quality, compliance and data integrity on local respectively global level of clinical trials
  • You provide internal medical and operational consultancy, advice and training on various aspects within clinical trials
4

Clinical Research Physician Resume Examples & Samples

  • Clinical research or pharmaceutical medicine experience preferred
  • Knowledge of drug development process preferred
  • Fluent in English; both written and verbal communications
  • Interpersonal, organizational and negotiation skills
  • Excellent teamwork skills
5

Clinical Research Physician, Immuno Resume Examples & Samples

  • Assist Lilly scientists with target identification and validation efforts guided toward development of new oncology therapeutics
  • Provide expertise to drug-discovery teams involved in clinical candidate selection overseeing laboratory to clinic transition of oncology compounds
  • Develop and implement medical aspects of global strategy and clinical plans for various oncology compounds
  • Interact with consultants, clinical pharmacologists, clinical investigators, and affiliate CRPs to plan, initiate, and conduct global clinical trials
  • Develop and/or review clinical trial protocols for clinical trialsand serve as medical lead for trial conduct
  • Collaborate on the statistical analysis and preparation of clinical study reports
  • Prepare and present documentation of clinical trial results to corporate committees, regulatory agencies, and outside audiences, and publish results of research projects
  • Provide support for global regulatory reports
  • Monitor safety reports and implement appropriate pharmacovigilance actions, if necessary
  • Establish and maintain contact with external experts and opinion leaders
  • Explore and pursue opportunities for extramural scientific relations
  • Attend and participate in scientific symposia as well as administrative and business workshops
  • Monitor global scientific/medical literature
  • Participate, as requested, as clinical expert on due diligence teams related to external in-licensing opportunities
  • Medical Doctor or Doctor of Osteopathy. Must be board eligible in oncology or hematology and have completed the comparable level of post-medical school clinical training relevant to the country of hiring. US trained physicians must have achieved board eligibility or certification. Foreign medical graduates who are not US board eligible or certified may be hired directly for employment in the US at the discretion of the Chief Medical Officer
  • Non-US trained physicians must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME). For the recognized list of foreign medical schools and the disapproved list, see http://www.in.gov/pla/2799.htm
  • Clinical experience in the field of medical oncology and experience with the clinical trial process, particularly with oncology phase I and phase II (proof-of-concept) studies
  • Clinical and/or scientific experience in cancer immunology
  • Knowledge of drug development process is preferred
  • Ability to influence others (both cross-functionally and within the function) in order to create a positive working environment
  • Willing to engage in domestic and international travel to the degree appropriate to support the business of the team
  • A scientific background in immunology with laboratory experience is desirable
6

Clinical Research Physician, Medical Affairs Resume Examples & Samples

  • Medical Doctor or Doctor of Osteopathy. Must be board eligible or certified in appropriate specialty/subspecialty or have completed the comparable level of post-medical school clinical training relevant to the country of hiring
  • Must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME). For the recognized list of foreign
  • Excellent English communication (written and verbal), interpersonal, organizational and negotiation skills
  • Demonstrated ability to influence others (both cross-functionally and within the function) in order to create a positive working environment. Demonstrated leadership and teamwork skills
  • Clinical and clinical trial expertise in GI cancer
  • Experience with lecturing, teaching, and/or writing about GI cancer
  • Translational research experience (e.g. biomarkers), particularly in GI cancer
  • Knowledge of the drug development process, particularly within the US
  • Pharmaceutical medicine experience
7

Clinical Research Physician Resume Examples & Samples

  • Provides subject matter expertise in medicine for all clinical research studies during the design and implementation phases of study protocols
  • Conducts physical, oral and other clinical assessments, with prospective and enrolled participants for research purposes only, as required by study protocols
  • Assists the study RN and study Principal Investigator, as needed, in determining participant eligibility for study enrollment and completion
  • Conduct follow-up calls/exams with research participants as may be specified by study protocols
  • In coordination with the study RN, respond to unanticipated and adverse events, and other medical emergencies as may arise
  • Review and contribute to the development of new or the updating of current clinical laboratory SOPs
  • Provides responsible, competent medical research advice to management
  • Treat as highly confidential, all data and information collected as part of day-to-day research operations
8

Temp / Clinical Research Physician Resume Examples & Samples

  • To provide medical safety and medical cover when monitoring study participants
  • To assess and interpret study clinical data, e.g. Pulse, BP, ECG’s, laboratory tests, adverse events etc
  • To provide medical support for human volunteer studies of new and existing pharmaceuticals
  • To assist in dosing of study medication
  • To work in accordance with ICH and GCP
9

Clinical Research Physician Resume Examples & Samples

  • Oversee safety issues of projects conducted by ICON which will include, but not be limited to, the following
  • Adverse event reporting to the sponsor
  • Follow up of adverse events as necessary
  • Communication of safety issues to the head of the department or designee
  • Participate in the on-call system for providing 24/7 medical support
  • Provide all necessary medical support functions as defined by project specific contractual obligations which will include, but not be limited to, the following
  • Medical information source
  • Ongoing training for project teams in therapeutic areas as requested
  • Review of study documentation (protocol, CRF. etc.)
  • Contribute to investigator meeting presentations
  • Ongoing safety review of individual patient laboratory reports generated by central laboratories
  • CRF safety review
  • Contribute any necessary medical input into integrated clinical and statistical reports
  • Assist in making presentations to potential clients when appropriate
  • Demonstrate a thorough understanding of ICON Standard Operating Procedures (SOPs) and ensure that all activities are conducted in accordance with current SOPs
  • Demonstrate a thorough understanding of applicable regulatory standards in the country where clinical studies are to be conducted and ensure that all activities are conducted in compliance with current regulations
  • Keep the person to whom the Clinical Research Physician reports informed of any issues within the department which require attention
  • Line management of DSAs as appropriate
  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
  • Medical degree (MBBS)
  • Preferably 2 years experience in a relevant clinical research role
  • Ability to medically evaluate clinical data
  • Good oral and written communication skills including proficiency in English
  • Ability and willingness to travel on an as-need basis
  • Good computer skills (MS: Outlook, Word, Excel)
10

Medical Director, Clinical Research Physician Resume Examples & Samples

  • Drive clinical trial protocol development and execution through regulatory filings
  • Prepare, present and manage materials for external advisory boards to guide protocol and product development
  • Provide medical guidance to investigators on managing patients on clinical protocols
  • Interact seamlessly with biomarker translational scientists to inform and refine clinical product development and strategy
  • Provide therapy area medical and scientific expertise to study teams and key stakeholders
  • Build and own investigator relationships across Europe for multiple indications and protocols
  • Provide clinical leadership to allow for initiation of trials in EU in collaboration with regulatory and clinical operations team members
  • Engage and inspire the project/clinical development team through communicating the strategic vision and the operational plan to achieve the vision
  • Provide input into clinical sections of IND’s, Investigator Brochures, CTA’s , ISS’, ISE’s and clinical expert reports
  • Represent the team with internal and external leaders and instill confidence in stakeholders by possessing a broad knowledge of the pharmaceutical industry and business environment and their impact on the product/therapy area
  • Work with Therapeutic Area Head and other team members to prepare abstract, manuscripts and presentation for external meetings as well as author clinical sections of regulatory documents (IB, IND sections)
  • Cultivate and nurture strong collaborations, relationships and support with Investigators, Academic partners and KOL’s
  • LI-SL1
  • Clinical expertise in the treatment and management of patients with hematologic malignancies and/or patients undergoing allogeneic stem cell transplant
  • Working knowledge of Good Clinical Practice and clinical research
  • Excellent written and spoken communication skills
  • Keen ability to analyze clinical efficacy, safety, and biomarker data
  • Interest/ability to evaluate early stage assets and participate in Business Development Due Diligence
11

Clinical Research Physician Resume Examples & Samples

  • 2 years clinical experience and/or two years of experience in clinical research coupled with an understanding of the International Conference on Harmonisation Good Clinical Practice (ICH GCP)
  • A flexible attitude with respect to work assignments, new learning and travel
  • Ability to manage multiple and varied tasks with enthusiasm, and prioritize workload with attention to detail
  • Willingness to work with multiple supervisors in a matrix environment, and to value the importance of teamwork
  • IT literate – Experience with Microsoft based applications and general knowledge of PC functions
12

Clinical Research Physician Resume Examples & Samples

  • Responsible for ensuring that the clinical trial is conducted according to the investigational plan and all applicable regulations
  • Provide medical and scientific feasibility of all new sponsor inquires
  • Direct test article administration or dispensation
  • Review and evaluate protocols and provide clinical and scientific support
  • Liaise with sponsor regarding study design and site capabilities
  • Interact with regulatory bodies as is relevant to clinical operations
  • Attend study initiation meetings
  • Present protocols at IRB/IEC meetings, as required
  • Assist Operations and Client Managers with sponsor visits
  • Perform pre-study physical examinations and review lab data to ensure volunteers are medically and mentally fit upon entering the study
  • Perform on-study and post-study physical examinations to ensure that the physical and mental wellbeing of volunteers is undiminished at the end of the study
  • Inform Principal Investigator, IRB and Sponsor as appropriate of relevant events
  • Review and sign CRFs at the conclusion of the study
  • Act as Principal Investigator/Co-Investigator as assigned by the Medical Director
  • 3-5 years MD experience
13

Clinical Research Physician Resume Examples & Samples

  • Previous clinical experience in direct patient care
  • Previous experience of performing a clinical research role within a clinical research organization or pharmaceutical company
  • Excellent written & verbal communication skills required including a good overall scientific vocabulary
  • Intermediate knowledge of Microsoft Word 2013, including the ability to troubleshoot issues
14

Medical Director, Clinical Research Physician Resume Examples & Samples

  • Provides Therapeutic Area expertise to study teams and key stakeholders
  • Participates in Development Strategy to make recommendations, take action and provide clinical research expertise
  • Ensures optimal study conduct; leads the clinical study, in liaison with the Clinical Trial Manager, from study set-up through study conduct until study closure and study report
  • Medical monitoring of clinical studies. Ability to review patient eligibility criteria, make medical decisions and regularly review/ monitor any possible safety issues
  • Provides medical, clinical and scientific guidance to the study team, affiliate medical personnel and investigative sites
  • Nurtures professional relationships with Investigators, Academic partners and KOLs
  • Maintains scientific expertise in Therapeutic Area concordant with current knowledge and practice
  • Provides high quality, current and timely medical/scientific input into sections of key documents relevant (IB, annual safety reports, etc) to the area of responsibility
  • Contributes to the planning and review of abstracts, manuscripts and presentations for external meetings
  • Presents at Internal and External Meetings, representing the team with internal and external leaders
  • Participates in activities of the multifunctional Disease Area team
  • Consolidated experience in the therapeutic area, including patient clinical experience
  • Experience in the design and execution of hematology protocols
  • Excellent written and verbal communication skills and interpersonal skills. Ability to advise, persuade and negotiate with colleagues in a supportive and encouraging fashion
  • Competencies related to the Clinical Development Process (Planning , coordinating and organizing, decision making, delivery of results, personal accountability, technical and professional knowledge, facilitating change)
  • Ability to understand and present data at internal and external meetings, including Investigators’ meetings and Data Review Meetings
  • Knowledge of the clinical development process and strong relationships with team members, colleagues and internal and external stakeholders to achieve results
15

Clinical Research Physician Resume Examples & Samples

  • Minimum master degree in clinical medicine or related bioscience
  • Knowledge of clinical development process, and regulatory requirements
  • Knowledge in industry setting
  • Interpersonal communication skill
  • Excellent written/verbal communication skills in English Team player
  • Project Management skill
  • Knowledge of PC (WORD, EXCEL, POWERPOINT)
  • Presentation skill
16

Clinical Research Physician Resume Examples & Samples

  • Medical Doctor or Doctor of Osteopathy
  • Preference will be given to candidates with internal medicine or endocrinology training
  • Must be Board eligible or certified in appropriate specialty/subspecialty or have completed the comparable level of post-medical school clinical training relevant to the country of hiring
  • Must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME). For the recognized list of foreign medical schools and the disapproved list, see http://www.in.gov/pla/2799.htm
  • Knowledge of drug development process relevant to country/region preferred
  • Demonstrated strong communication, interpersonal, teamwork, organizational and negotiation skills
  • Demonstrated ability to influence others (both cross-functionally and within the function) in order to create a positive working environment
  • Ability to engage in domestic and international travel to the degree appropriate to support the business of the team
  • Medical affairs experience
  • Demonstrated strong communication,, interpersonal, teamwork, organizational and negotiation skills
  • Not a requirement but highly desirable---Knowledge in immunology and/or cardiovascular medicine
17

Clinical Research Physician Resume Examples & Samples

  • Provides leadership to the clinical study team involved in the execution of clinical studies
  • Oversees and is responsible for the quality, coordination and timeliness of protocol development
  • Oversees and is responsible for the quality, coordination, medical accuracy and timeliness of clinical study reports
  • Assists senior management to oversee quality, coordination and timeliness of clinical sections of INDs, Investigator Brochures, CTAs, ISS's, ISE's, and clinical expert reports
  • Participates, as required, as a clinical representative on Project Teams
  • Establishes and maintains working relationship with Study investigators, key opinion leaders, academicians, and Senior managers and department heads across the corporation
  • Ensures adherence to GCP/ICH and SOP standards
  • Maintains clinical and scientific awareness in area of expertise. Supports clinical operations in site selection, study budget preparation, study execution and addresses clinical/medical issues at study sites
  • Participates in the organization, coordination and execution, as required, of internal meetings and external medical/scientific meetings, e.g., Investigator Meetings and clinical/scientific advisory board meetings
  • Develops and gives oral presentations, as required
  • Supports data management as required for CRF development, database edit checks development, listings review, query resolution, database clean-up and lock activities
  • Prepares clinical study timelines and status reports, as required, per Supervisor
18

Clinical Research Physician Resume Examples & Samples

  • MD plus completion of Fellowship program
  • Physicians trained outside the US who are not US board eligible or certified may be hired directly for employment in the US at the discretion of the Chief Medical Officer. Non-US trained physicians must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME)
  • Must be able to demonstrate basic knowledge of the drug development process and exercise Good Clinical Practice (ICH GCP) principles
  • Must be fluent in English; both written and verbal communications
  • Able to demonstrate strong communication, interpersonal, organizational, and negotiating skills
  • Able to engage in domestic and international travel to the degree appropriate to support project and business needs
  • Previous research experience – basic and/or translation is desirable
  • Demonstrated experience and involvement in clinical trial design or execution
  • Regulatory experience in support of INDs, BLAs, NDAs, supplemental applications etc. is desirable
19

Senior Clinical Research Physician Resume Examples & Samples

  • Leading the clinical team activities providing expertise and significant contributions to Clinical Project Teams, Study Teams, Global Development Teams and Global Brand Teams
  • Preparing clinical development plans and institute properly approved clinical protocols. Presenting and defend protocols. Implement clinical R&D policies, SOPs and related directives
  • Monitoring study progress, leading the analyses and data evaluation process for progress reporting and presentations to senior management
  • Preparing various official and regulatory documents for Regulatory and other agencies, such as Dossiers, NDAs, INDs, Safety and Annual reports, handling of responses to regulatory agencies regarding questions about complex safety or efficacy issues
  • Serving as the Medical Monitor, responsible for the safety monitoring of clinical trials, and as medical expert for Phase I-II studies, managing the process from protocol development thorough individual study report and integrated regulatory documentation
  • Ensuring that Serious Adverse Events are properly reported on a global basis
  • Leading cross-functional teams comprised of multidisciplinary professionals and clinical scientists. Directing responsibility for leading a team of Clinical Development professionals and ensure delivery of their portfolio of assets
  • Reviewing potential in-licensing candidates and present recommendations to Senior Management groups
  • Supporting any needed due diligence and prepare/present medically sound strategy and plans associated with advanced opportunities
  • Contributing and support Department/Clinical initiatives to improve the quality and content of all clinical programs as well as the cross functional/organization processes designed to effectively deliver our R&D portfolio
  • M.D. degree or equivalent, board certified (or eligible). Medical specialty and sub-specialty training and certification are required in Diabetes / Endocrinology
  • Diabetes / Obesity / NASH therapy experience
  • Significant experience in clinical research and/or endocrine drug development in pharmaceutical or CRO environment
  • Excellent oral and written communication skills; strong interpersonal and listening skills
  • Proven leadership skills and demonstrated ability to interact collaboratively in a cross-functional environment
  • Ability to make sound and timely decisions; agile in learning and action oriented
  • High level of emotional intelligence; able to deal with ambiguity
  • Able to relate to varied level audiences across organisation; able to build and lead effective teams and coach & develop team members; able to set priorities for team and maintain accountability; skilful in negotiating organisational boundaries and hierarchy; experience managing and developing others
  • Clinical or research experience in field of specialisation
  • A fellowship or training and certification in Endocrinology
20

Clinical Research Physician, Diabetes Resume Examples & Samples

  • Must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME). For the recognized list of foreign medical schools and the disapproved list
  • Three to 5 years of clinical care and clinical research or pharmaceutical medicine experience
  • Pediatric Endocrinology experience preferred including diabetes and growth hormone deficiency treatment
  • Demonstrated ability to balance scientific priorities with business priorities
  • Fluent in English, verbal and written communication
21

Clinical Research Physician Resume Examples & Samples

  • Responsible for protecting the rights, safety and welfare of participants under their care
  • Administers test article to the subjects, or delegates this to nursing staff where appropriate
  • Perform pre-study physical examinations and review lab data and all inclusion/exclusion criteria to ensure volunteers are medically and mentally fit upon entering the study
  • Perform on-study and post-study physical examinations to ensure that the physical and mental well being of volunteers is undiminished at the end of the study
  • Inform Principal Investigator, IRB/IEC and Sponsor as appropriate of relevant events
  • Delegate the above as appropriate
  • Typically 2 years MD experience
  • Needs to have at least 2 years experience in clinical training posts
  • Previous CRO or Phase I experience preferred but not required