Clinical Research Expert
4 days ago
At George Clinical, we're dedicated to advancing clinical research through scientific expertise and operational excellence. Our full-service Contract Research Organization (CRO) is committed to delivering better research outcomes for millions worldwide.
We prioritize people, ensuring diverse, representative patient recruitment and combining global reach with local knowledge. This enables us to build trust with local communities and deliver faster results.
About the RoleAs a Senior Medical Monitor, you'll play a critical role in ensuring the safety and integrity of clinical trials. You'll provide medical and scientific expertise to clinical research projects, collaborating closely with cross-functional teams to support study execution and compliance with regulatory requirements.
- Ensure patient safety and adherence to protocol.
- Serve as the primary medical contact for study teams, investigators, and sponsors.
- Review and assess adverse events, serious adverse events (SAEs), and safety reports.
- Contribute to protocol development, study design, and medical monitoring plans.
- Participate in investigator meetings, site initiation visits, and data monitoring activities.
- Support regulatory submissions by providing expert medical input.
- Collaborate with clinical operations, biostatistics, and regulatory teams to drive successful trial outcomes.
To succeed in this role, you'll need:
- A Medical Doctor (MD) qualification.
- At least 5 years of experience as a Medical Monitor in clinical trials.
- Strong knowledge of GCP, ICH guidelines, and regulatory requirements in the APAC region.
- Experience in safety monitoring, adverse event assessments, and medical data review.
- Excellent communication and collaboration skills.
- Ability to provide strategic medical insights and problem-solving expertise.
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