Clinical Data Coordinator - Trials Support & Compliance

McKesson Corporation; Denver (CO); On-site; USD 33,062 - 37,195; Full time

Job summary

McKesson Corporation in Denver, Colorado, is looking for a Data Coordinator to support clinical research activities. Responsibilities include assisting the Clinical Research Coordinator and Research Nurse, maintaining regulatory files, and ensuring adherence to Good Clinical Practice (GCP) guidelines.

The ideal candidate should be detail-oriented with a firm understanding of scientific and medical terms, and possess excellent written and oral skills in English. A Bachelor Degree is preferred along with experience in the healthcare or pharmaceutical sector.

Qualifications

• Knowledge of GCP and Good Manufacturing Practice (GMP).
• Detail-oriented with excellent communication skills.
• Experience in clinical trials or pharmaceutical industry preferred.

Responsibilities

• Support CRC to meet industry trial data deadlines.
• Obtain source documentation for patients in trials.
• Assist with case report form completion.
• Track Serious Adverse Events (SAE).
• Maintain patient visit tracking spreadsheets.
• Archive study and regulatory files.
• Ensure accuracy of source document templates.

Skills

Knowledge of scientific, medical, and regulatory terms

Attention to detail

Excellent English written and oral skills

Experience in healthcare or clinical trials

Education

Bachelor Degree preferred

Job description

McKesson Corporation in Denver, Colorado, is looking for a Data Coordinator to support clinical research activities. Responsibilities include assisting the Clinical Research Coordinator and Research Nurse, maintaining regulatory files, and ensuring adherence to Good Clinical Practice (GCP) guidelines.

The ideal candidate should be detail-oriented with a firm understanding of scientific and medical terms, and possess excellent written and oral skills in English. A Bachelor Degree is preferred along with experience in the healthcare or pharmaceutical sector.