Medical Monitor – Clinical Trials (U.S.)
Company: Umbrex Agency
- Location: United States
- Work mode: Remote
- Seniority: Senior
- Employment type: Contract
- Posted: 2 days ago
- Offer language: English
Job description
Our client is a biopharmaceutical company seeking an experienced Medical Monitor to provide medical and clinical oversight for ongoing clinical trials, potentially in oncology. The consultant will be responsible for reviewing clinical trial data, addressing medical and safety issues, collaborating with internal study teams, and supporting clinical trial planning and execution.
Key Responsibilities:
- Provide medical monitoring and clinical oversight for ongoing clinical trials
- Review and interpret clinical trial data to ensure patient safety and study integrity
- Assess, triage, and address medical and safety issues arising during clinical trials
- Collaborate with internal clinical development and study teams to support trial execution
- Contribute to clinical study planning, endpoint design, and medical oversight activities
Qualifications:
- Prior experience serving as a Medical Monitor for clinical trials at a biopharmaceutical company or Contract Research Organization (CRO) (required)
- MD or DO qualification with extensive clinical trial experience (preferred)
- Experience providing medical oversight for oncology clinical trials (a plus)
- Strong understanding of clinical trial operations, medical monitoring, and patient safety
- Excellent clinical judgment, communication, and cross-functional collaboration skills
Start Date: ASAP
Duration: Approximately 6 months
Time Commitment: 5 days per week
Location: Remote (U.S.)
Expected rate: Client did not provide a range
Project ID: 9815
***This is a contract role and does not offer any health benefits.
