Clinical Research Physician Resume

When writing a Clinical Research Physician Resume remember to include your relevant work history and skills according to the job you are applying for. Whether you're seeking an entry-level position or have been in your career for a few years, exposing your relevant achievements in your resume can allow you to stand out and get that job interview.

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Here is the Clinical Research Physician Resume example:

John Wright

3015 Meadowview Drive

Covington, VA 24426

(555)-555-5555

[email]

Job Objective To obtain a Clinical Research Physician position that fully utilizes my experience and abilities.

Highlights of Qualifications:

Highly experienced in handling and delivering clinical research-based medical services
Profound knowledge of Good Clinical Practices, clinical research and clinical terminology
Outstanding knowledge of FDA guidelinesand international regulatory requirements
Familiarity with clinical trial preparation and drug development process
Ability to design and execute effective clinical trial strategies
Ability to handle and interact with aged and chronically ill patients in a considerate manner

Professional Experience:

Clinical Research Physician

Massachusetts General Hospital (GHC), Covington, VA

August 2012 – Present

Responsibilities:

Developed and implemented medical strategies, clinical development plans, and clinical therapy trials.
Informed participants about potential risks and monitored their health conditions throughout the trial process.
Conducted, interpreted, and reported on various laboratory studies and diagnostic tests.
Interacted and liaised with various industry peers and clinical research organizations.
Performed physical assessment of patients and provided appropriate treatment.
Built and maintained strong professional relationships with research partners, sponsors, and participants.

Clinical Research Physician

Ironwood Pharmaceuticals, Inc., Covington, VA

May 2009 – July 2012

Responsibilities:

Interacted and worked with clinical research staff in a collaborative manner.
Planned, executed, and reported on clinical trials and research activities.
Developed and implemented clinical research protocols and data collection requirements.
Prepared, reviewed, and provided study reports, publications and regulatory reports.
Identified and reported adverse events as per patient safety guidelines.
Interpreted and adhered to Good Clinical Practices and other related laws and requirements.

Education

Doctor of Medicine

Mayo Medical School, Rochester, MN