- Assist in clinical development planning and execution.
- Oversee clinical development activities in medical monitoring and medical writing.
- Provide critical medical and clinical insights to projects.
- Review clinical protocol design and oversee trial execution monitoring.
- Ensure subjects' well-being throughout the study.
- Ensure compliance with clinical development plans and regulations.
- Contribute to medical writing for study-related documents.
- Conduct literature searches and interpret findings.
- Assist with sponsor visits.
- MD degree or equivalent in life sciences.
- Minimum 5 years of experience in biopharmaceutical industry.
- Active US Medical License.
- Extensive experience in medical monitoring.
- Strong background in providing medical and scientific advice on clinical trial protocol design and development strategies.
- Critical thinking and scientific acumen.
- Excellent organizational, interpersonal, and communication skills.
- Proficiency in English, both written and verbal.
- Oncology experience preferred.
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Medical Director/Medical Monitor - South San Francisco, United States - Meet Recruitment
Description
Meet has partnered with a globally oriented clinical research organization (CRO), with expanding operations in the US. They are on the lookout for a seasoned Medical Monitor to join their team.
As a Medical Monitor, you'll play a pivotal role in supporting clinical development planning and execution to meet their clients' project requirements and quality standards. Collaborating with key functions such as clinical operations, biometrics, quality assurance, and pharmacovigilance, you'll provide clinical expertise to manage project-related medical monitoring. This includes delivering high-quality clinical scientific services, contributing medical input to protocols, conducting medical writing, and fostering strong medical science relationships both internally and externally.
Key Responsibilities:
Qualifications: