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Medical Sciences Consultant
2 weeks ago
We value innovative thinking and expertise at George Clinical. As a Senior Medical Monitor, you will play a crucial role in ensuring the safety and integrity of clinical trials.
You will provide medical and scientific expertise to clinical research projects, working closely with cross-functional teams to support study execution and compliance with regulatory requirements.
Your Key Responsibilities
- Provide medical oversight for clinical trials, ensuring patient safety and adherence to protocol.
- Collaborate with cross-functional teams to support study execution and compliance with regulatory requirements.
- Develop and implement medical monitoring plans for clinical trials.
- Assess and report on adverse events, serious adverse events (SAEs), and safety reports.
- Support regulatory submissions by providing expert medical input.
- Participate in investigator meetings, site initiation visits, and data monitoring activities.
About This Opportunity
This is an exciting opportunity to join our team and contribute to advancing clinical research. If you have a strong background in medicine and clinical trials, excellent communication skills, and experience working in a cross-functional team environment, we encourage you to apply.
What We Offer
- A competitive salary and benefits package.
- The opportunity to work on diverse projects and collaborate with global teams.
- Access to professional development opportunities and training.
- A supportive and inclusive work environment.
