Senior Clinical Trial Management Specialist

1 week ago


California, United States R&D Partners Full time

R&D Partners is seeking a Senior Clinical Trial Management Specialist with expertise in biosample oversight to enhance our client's operations in the pharmaceutical sector. This role offers a hybrid work arrangement, requiring three days on-site weekly.

Position Overview:

  • Oversee and coordinate all logistical aspects related to the collection, transportation, and evaluation of biological specimens within clinical studies.
  • Ensure adherence to project timelines, including necessary documentation and stakeholder communications.
  • Act as the primary liaison for both internal teams and external partners to facilitate the effective execution of biological sample analysis strategies.
  • Engage in the examination of study protocols and related documentation, such as clinical sample management plans and communication strategies for study meetings.
  • Contribute to the development of standard operating procedures (SOPs) and participate in various special initiatives.

Qualifications:

  • A Bachelor’s degree in Life Sciences, accompanied by over five years of experience in the biopharmaceutical industry.
  • Proven track record in biosample management.
  • Familiarity with FDA regulations and ICH-GCP standards.

Compensation:

  • Hourly rate of $56-$58, commensurate with experience.

R&D Partners specializes in providing employment opportunities within leading pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

R&D Partners is committed to equal employment opportunities.



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