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Clinical Research Associate Manager
1 week ago
About the Role:
We are seeking a highly skilled and experienced Clinical Research Associate to join our team at Medpace. As a CRA, you will be responsible for conducting qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol.
Your Key Responsibilities Will Include:
- Verifying adequate investigator qualifications, training, and resources, including facilities, laboratories, equipment, and staff;
- Medical record and research source documentation verification against case report form data;
- Regulatory document review;
- Investigational product/drug accountability and inventory;
- Verification and review of adverse events, serious adverse events, concomitant medications, and corresponding illnesses;
- Assessing the clinical research site's patient recruitment and retention success;
- Completion of monitoring reports and follow-up letters.
About You:
To be successful in this role, you will have a Bachelor's degree in a health or science-related field and at least 1.5 to 5 years of experience in clinical monitoring. You will also need to be knowledgeable about Clinical Monitoring practices and procedures.
What We Offer:
At Medpace, we provide comprehensive initial and ongoing training to ensure your success as a CRA. Our PACE Training Program will prepare you to effectively carry out your duties and enhance your current abilities. You will also have opportunities to participate in other clinical research departmental core rotations and learn other aspects of the drug/device development and approval process.
