Data Coordinator
About the role
The Data Coordinator supports the Study Coordinator in ensuring all activities are conducted according to company SOPs, GCP, and ICH regulations and guidelines. Key responsibilities include:
- Supporting the Study Coordinator in meeting industry trial data deadlines.
- Obtaining source documentation for patients enrolled in clinical trials.
- Aiding in case report form completion and query resolution.
- Assisting in Serious Adverse Event (SAE) reporting and tracking.
- Maintaining and archiving study administrative files.
- Creating and managing patient visit tracking spreadsheets.
- Assisting with special procedural projects to enhance Drug Development Data Operations.
- Auditing adherence to SOPs, GCP, and ICH regulations and guidelines during the clinical trial conduct.
Requirements
Knowledge of scientific, medical, and regulatory terms.
Detail-oriented.
Excellent English written and oral skills.
Bachelor's degree preferred.
Healthcare experience, clinical trials support, or pharmaceutical industry experience preferred.
Qualifications
Knowledge of scientific, medical, and regulatory terms.
Detail-oriented.
Excellent English written and oral skills.
Skills
Knowledge of GCP and Good Manufacturing Practice (GMP).
Benefits
Comprehensive benefits package including physical, mental, and financial well-being support.
Competitive compensation package with potential for annual bonuses and long-term incentives.
Total Rewards offerings tailored to the diverse colleague population.
Equal opportunity employer.
Note: Online recruiting-related scams involving McKesson are common. Candidates should only engage with official recruiters through the company’s career site: careers.mckesson.com.