Job Details

It’s More Than a Career, It’s a Mission.

Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the largest community-based cancer programs to advance oncology treatments and improve outcomes for cancer patients across the globe. We look for mission-driven candidates who have a desire to advance the fight against cancer and make a difference in the lives of patients diagnosed with cancer every day.

Our Mission

People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.

As the Source Document Specialist you will provide support to the Study Coordinator on a daily basis, ensure all activities are conducted according to company SOPs, and all applicable GCP and ICH regulations and guidelines.

• You will support the Study Coordinator to meet industry trial data deadlines.

• You will obtain source documentation for patients enrolled into clinical trial.

• You will assist the Study Coordinator with case report form completion if needed.

• You will assist the Study Coordinator with query resolution if needed.

• You will assist the Study Coordinator to obtain medical record including research chart.

• You will create and maintain spreadsheet for medical record and research chart accountability.

• You will maintain and archive study administrative files.

• You will work closely with Tennessee Oncology medical record departments to assure accountability of records.

• You will work closely with Iron Mountain to locate archived records.

• You will meets with project manager on a regular basis.

• You will assesses adherence to Sarah Cannon SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines.

What you should have for this role:

• An Associate Degree; Bachelor Degree preferred

• At least 2 years of experience working in health care organization – oncology preferred

• 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, or pharmaceutical industry experience preferred

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.