Data Coordinator

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

Job summary

McKesson’s Corporate in Denver, Colorado, is seeking a Data Coordinator to support the Clinical Research Coordinator and Research Nurse. This role ensures daily activities comply with company SOPs and relevant regulations.

The ideal candidate will have knowledge of scientific and regulatory terms, be detail-oriented, and possess excellent communication skills. A bachelor’s degree is preferred along with experience in healthcare or clinical trials support.

The position offers a salary range of $24/hr to $27/hr.

Qualifications

• Knowledge of scientific, medical, and regulatory terms.
• Knowledge of GCP and Good Manufacturing Practice (GMP).
• Detail-oriented with excellent communication skills.
• Healthcare experience or clinical trials support preferred.

Responsibilities

• Support CRC to meet industry trial data deadlines.
• Obtain source documentation for patients enrolled onto clinical trials.
• Assist with case report form completion.
• Assist in Serious Adverse Event (SAE) reporting.
• Create patient visit tracking spreadsheets.
• Maintain and archive study and regulatory files.

Skills

Knowledge of scientific, medical, and regulatory terms

Knowledge of GCP and Good Manufacturing Practice (GMP)

Detail-oriented

Excellent English written and oral skills

Healthcare experience

Clinical trials support

Pharmaceutical industry experience

Education

Bachelor's Degree preferred

Job description

Role Overview

The Data Coordinator provides support to the Clinical Research Coordinator (CRC) and Research Nurse on a daily basis, ensuring all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines.

Responsibilities

• Support CRC to meet industry trial data deadlines.
• Obtain source documentation for patients enrolled onto clinical trials.
• Assist CRC with case report form completion and query resolution.
• Assist in Serious Adverse Event (SAE) reporting and tracking.
• Create and maintain patient visit tracking spreadsheets for CTS.
• Maintain and archive study administrative files.
• Maintain and archive regulatory files.
• Assist in ensuring source document templates are accurate.
• Be assigned special procedural projects to enhance the functioning of the research program.
• Assess adherence to SCRI SOPs, GCP, and ICH regulations throughout the conduct of the clinical trial.

Qualifications

• Knowledge of scientific, medical, and regulatory terms.
• Knowledge of GCP and Good Manufacturing Practice (GMP).
• Detail‑oriented.
• Excellent English written and oral skills.
• Bachelor's Degree preferred.
• Healthcare experience, clinical trials support, or pharmaceutical industry experience preferred.

Compensation

Salary range: $24/hr – $27/hr.

Equal Opportunity Employer

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.