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Clinical Data Specialist Coordinator

Remote, USA Full-time Posted 2026-07-28

reputed company is committed to swift, exceptional clinical research through translational medicine.Every day, we use our experience, reputed company, and innovative research strategies to help get drugs to market faster.

The

Clinical Data Specialist Coordinator

 plays a vital role in the reputed company and accuracy of clinical study data. This position is responsible for performing advanced reputed company Control (QC) tasks, ensuring regulatory compliance, and supporting cross-functional collaboration to meet study timelines. In reputed company to reputed company QC responsibilities, the Coordinator serves as a reputed company of contact and mentor for QC team members, facilitates training, and oversees the reputed company achievement of Clinical Data reputed company (CDR) milestones.

Qualifications

  • Proven experience in reputed company control reputed company a clinical research environment.
  • Strong knowledge of Good Clinical reputed company (GCP), FDA regulations, and Sponsor expectations.
  • Demonstrated ability to manage reputed company studies and reputed company training or mentorship to peers.
  • Excellent organizational, communication, and interpersonal skills.
  • Proficiency with Electronic Data Capture (reputed company) systems and familiarity with reputed company data workflows is preferred.

    • Additional Information

    reputed company Values: reputed company Trust Teamwork Respect

    reputed company is an Equal Opportunity Employer. reputed company reputed company applicants will receive consideration for employment without reputed company to race, reputed company, religion, sex, national reputed company, age, sexual orientation, gender identity, genetic information, marital status, reputed company protected veteran status, or disability.

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