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Senior Clinical Trial Management Specialist

2 months ago


California, United States R&D Partners Full time

Our esteemed pharmaceutical client in the Bay Area is seeking a Senior Clinical Trial Management Specialist with expertise in biosample oversight to enhance their dynamic team. This role offers a hybrid work arrangement, requiring three days on-site each week.

Position Overview:

  • Oversee and coordinate all operational processes necessary for the collection, transportation, and evaluation of biological samples throughout the clinical trial lifecycle.
  • Manage project timelines, ensuring all documentation and communications are meticulously maintained.
  • Act as the primary liaison with both internal and external parties to ensure the effective execution of the biological sample analysis strategy.
  • Engage in the examination of study protocols and other related documents, including the clinical sample management plan and study communication strategies, as well as presentations for Investigator and/or study initiation meetings.
  • Contribute to the development of Standard Operating Procedures (SOPs) and engage in special projects as required.

Qualifications:

  • A Bachelor’s degree in Life Sciences coupled with over five years of experience in the biopharmaceutical sector.
  • Proven track record in biosample management.
  • Familiarity with FDA regulations and ICH-GCP guidelines.

Compensation:

  • $56-$58/hour (Dependent on Experience)

R&D Partners is a specialized employment agency and recruitment firm dedicated to providing career opportunities within leading pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

R&D Partners is committed to equal opportunity employment.