
Clinical Research Expert
1 week ago
As a Clinical Research Physician, you will play a pivotal role in ensuring the integrity and safety of clinical trials. Your expertise in medical monitoring, pharmacovigilance, and regulatory reporting will be instrumental in guiding operational teams, investigators, and study sites.
- Provide medical oversight of adverse events, lab data, concomitant medications, and protocol adherence.
- Offer scientific and medical guidance to operational teams, investigators, and study sites.
- Collaborate with Pharmacovigilance on safety assessments, SAE narratives, and regulatory reporting.
- Support independent committees (DSMBs, adjudication committees) as needed.
- Conduct ongoing patient profile and CRF reviews to ensure clinical integrity and safety.
Requirements:
- A medical degree (MD) with advanced clinical training and at least 3 years' experience in pharma/clinical research.
- Prior medical monitoring experience in a contract research organization (CRO) is preferred.
- Strong communication, analytical, and problem-solving skills.
- Experience in late-stage (Phase II/III) clinical trials.
What We Offer:
- A competitive salary and comprehensive benefits package.
- A diverse culture that rewards high performance and nurtures talent.
At Our Organization:
- We are committed to providing an inclusive and accessible environment for all candidates.
- We offer equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Searchable Terms:
- Clinical Research Physician
- Medical Monitoring
- Pharmacovigilance
- Regulatory Reporting
- Late-Stage Clinical Trials
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