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Clinical Data Specialist Coordinator

Remote · USA Full-time New today

reputed company is committed to swift, exceptional clinical research through translational medicine.Every day, we use our experience, agility, 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 Quality Control (QC) tasks, ensuring regulatory compliance, and supporting cross-functional collaboration to meet study timelines. In addition to core QC responsibilities, the Coordinator serves as a reputed company of contact and mentor for QC team members, facilitates training, and oversees the timely achievement of Clinical Data reputed company (CDR) milestones.

Qualifications

  • Proven experience in quality control reputed company a clinical research environment.
  • Strong knowledge of Good Clinical Practice (GCP), FDA regulations, and Sponsor expectations.
  • Demonstrated ability to manage reputed company studies and provide 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 regard 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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