Clinical Operations Specialist
2 weeks ago
Sr. Clinical Trial Management Associate (Senior CTMA)
Job Summary:We are seeking a highly skilled and experienced Sr. Clinical Trial Management Associate to join our Clinical Operations team in Foster City, CA. As a key member of our team, you will be responsible for managing the execution of clinical trials across all Gilead therapeutic areas.
Key Responsibilities:- Lead or manage components of Phase I, II, or III studies
- Assist in the review of clinical study protocols and other study documents
- Participate in the development of SOPs and contribute to special projects
- Manage study timelines, including documentation and communications
- Coordinate all operational activities required for the collection, delivery, and analysis of biological samples within a clinical trial
- MA/MS/PharmD/PhD with 2+ years' relevant clinical or related experience in life sciences
- BA/BS/RN with 4+ years' relevant clinical or related experience in life sciences
- Experience in managing the work of external vendors
- Meets all requirements for Clinical Trial Management Associate (CTMA) grade 25 position with demonstrable proficiency
- Demonstrated ability to be a fast learner
- Demonstrated ability to be flexible and adaptable to change
- Knowledge of full cycle clinical study management, from start-up to close-out
- Significant industry knowledge
We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
How to Apply:Please submit your resume and cover letter to [insert contact information].
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