Data Coordinator

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

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

Responsibilities

• You will support CRC to meet industry trial data deadlines
• You will obtain source documentation for patients enrolled onto clinical trials
• You will assist CRC with case report form completion and with query resolution
• You will assist in Serious Adverse Event (SAE) reporting and tracking
• You will create and maintain patient visit tracking spreadsheets for CTS
• You will maintain and archive study administrative files
• You will maintain and archive regulatory files
• You will assist in ensuring source document templates are accurate.
• You will be assigned special procedural projects to enhance the functioning of the research program
• Throughout the conduct of the clinical trial you will assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines.

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 Degree preferred
• Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred

The compensation range for this position is $24/hr - $27/hr.

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.