Clinical Project Manager and Site Supervisor
3 days ago
We are seeking a highly skilled Clinical Project Manager and Site Supervisor to join our team at Tigermed. As a key member of our clinical operations department, you will be responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies.
About the Role- Project Management: Responsible for managing clinical projects from initiation to close-out, ensuring timely completion and within budget.
- Study Site Management: Selects eligible sites, conducts pre-study visits, initiates studies, and monitors sites to ensure compliance with regulations and protocols.
- Documentation: Ensures timely collection and maintenance of essential documents, including investigator files and trial master files.
- Develop and implement project plans, timelines, and budgets in collaboration with cross-functional teams.
- Coordinate with sites, sponsors, and vendors to ensure smooth study execution.
- Monitor and report on project progress, identifying and mitigating risks as needed.
- Select and initiate study sites, ensuring they meet sponsor selection criteria.
- Conduct pre-study visits to assess site capabilities and prepare for study start-up.
- Ensure site staff is adequately trained on study protocols and procedures.
- Monitor site performance, addressing issues and completing visit reports in a timely manner.
- Bachelor's degree in Medical, Pharmacology, or Biology-related field.
- At least 1 year of experience as a CRA (Clinical Research Associate).
- Excellent understanding of Good Clinical Practice (GCP) and clinical trial operations.
- Strong skills in Microsoft Office applications, including Word, Excel, PowerPoint, and Outlook.
The estimated annual salary for this position is $80,000-$110,000, depending on experience and qualifications. Additional benefits include health insurance, retirement plan, and paid time off.
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