Medical Research Coordination Professional
5 days ago
This role offers a unique opportunity to make a difference in the lives of patients and families facing various diseases. As a Clinical Research Associate, you will be responsible for conducting site visits, communicating with site staff, and verifying investigator qualifications and resources.
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Responsibilities:\
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- Conduct qualification, initiation, monitoring, and closeout visits at research sites;\
- Communicate with site staff, including coordinators, clinical research physicians, and their site staff;\
- Verify adequate investigator qualifications, training, and resources;\
- Medical record and research source documentation verification against case report form data;\
- Verification that the investigator is enrolling only eligible subjects;\
- Regulatory document review;\
- Medical device and/or investigational product/drug accountability and inventory;\
- Verification and review of adverse events, serious adverse events, concomitant medications, and corresponding illnesses;\
- Assess clinical research sites' patient recruitment and retention success and offer suggestions for improvement;\
- Completion of monitoring reports and follow-up letters.\
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Requirements:\
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- A minimum of a Bachelor's degree in a health or science-related field; BSN preferred;\
- Ability to travel 60-70% to locations nationwide (or less if remote/virtual visits are required);\
- Maintenance of a valid driver's license and ability to drive to monitoring sites;\
- Minimum 1 year of healthcare-related work experience preferred;\
- Proficient knowledge of Microsoft Office;\
- Strong communication and presentation skills;\
- Detail-oriented and efficient in time management.\
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Why Join Medpace?\
At Medpace, we prioritize our employees' growth and well-being. We offer a comprehensive benefits package, flexible work schedules, and professional development opportunities.
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