Job Description

Our drug development client, is looking for an experienced research physician to join their well established clinical trial department.This position will be doing phase I of clinical research trials for CRO. The person we are looking for will need to be BC in Family or Internal Medicine. This person does not have to have experience in phase one but will need to have some experience in clinical research. This position is for a person who wants to learn and be groomed into a position which will eventually take over as a medical director in 5 or 6 years from now. \
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Job Functions\
Works closely with the Medical Director to develop and implement policies and procedures that ensure high quality service.\
As Principal Investigator and as signatory on FDA Form 1572, provides oversight to all staff who are directly involved in study execution.\
Functions as the Principal Investigator or Sub-Investigator for Clinical Research Studies, ensuring that all protocol guidelines are met.\
Provides medical safety review of clinical research protocols as requested by Sponsors.\
Responsible for protecting the rights, safety and welfare of study participants enrolled in a clinical research study.\
Responsible for ensuring that the clinical trial is conducted according to the investigational plan and that it meets all the applicable regulations, including adherence to Good Clinical Practices and Standard Operating Procedures (SOPs).\
Provides medical and scientific feasibility of all new sponsor inquiries.\
Attends study initiation meetings and communicates with the IRB when required.\
Maintains external relationships with physicians, hospitals and community health centers to assist with study needs and participant recruitment.\
Conducts Physical Exams on study participants.\
Evaluates clinical laboratory and study examinations.\
Monitors and documents all participants adverse events, medical condition and response to study medications and treatments.\
Specialty in Internal Medicine, Emergency Medicine, or Family Medicine.\
Minimum of 2 years executive-level leadership experience.\
Maintains current DEA license.\
Maintains current ACLS certification.\
Should have at least several peer reviewed academic publications as primary author in the field of clinical pharmacology, concerned with pharmacokinetic and/or pharmacodynamic investigations.\
Huge Plus if you have experience with carbon 14 studies\
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Pursues clients and responds to client requests.\
Attends industry events to ensure optimum exposure of company, Inc.\
Senior Research Physicians completes the above essential functions in addition to acting as subject matter expert in clinical pharmacology, works closely with company sponsors, planning and executing Phase I and Phase II drug development projects.
Employment Type: Full-Time

Job Tags

Full time,

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