Clinical Operations Specialist

2 weeks ago


San Mateo, California, United States RICEFW Technologies, Inc. Full time
Job Title:

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
Requirements:
  • 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
Preferred Qualifications:
  • 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
What We Offer:

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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