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Source Document Specialist

McKesson Corporation

Nashville, TNFull-timePosted 2w agoStill listed today

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At a glance

Compensation
No compensation found
Location
Nashville, TN
Schedule
Full-time
Work Authorization
Not specified

Olive lists jobs from US employers, including remote roles you can work from the United States.

Requirements

Credentials this posting asks for.

Associate's degree, required

Job overview

The Source Document Specialist supports the Study Coordinator with clinical-trial documentation and administrative activities. The role obtains patient source documents and medical records, assists with case report forms and query resolution, and maintains record-accountability spreadsheets and study files. It also coordinates with medical-record departments and archive services, and assesses adherence to company SOPs, GCP, and ICH regulations and guidelines.

Skills & qualifications

RequiredNice to have

Skills

Scientific Terminology, nice to haveMedical Terminology, nice to haveRegulatory Terminology, nice to haveGood Clinical Practice, nice to haveGood Manufacturing Practice, nice to haveAttention to Detail, nice to haveEnglish Writing, nice to haveEnglish Oral Communication, nice to have

Qualifications

Associate Degree, requiredBachelor's Degree, nice to have2 Years Healthcare Experience, requiredOncology Experience, nice to haveHealthcare Experience, nice to haveClinical Trials Support Experience, nice to havePharmaceutical Industry Experience, nice to have

Full job description

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 meet with project manager on a regular basis.
  • You will assess 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

About Sarah Cannon Research Institute

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 850 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA in the past decade. SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S. Please click here to learn more about our research offerings.

We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here.

As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:

McKesson Talent Advisors will never solicit money or credit card information in connection with a McKesson job application.

McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.

McKesson job postings are posted on our career site: careers.mckesson.com.

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.

How this job compares

Set against the 1,460 open Clinical Research jobs on Olive Jobs, counted November 11, 2026.

Pay
  • This postingNot listed
  • US median$130–198K/yr719 salary ranges
  • US median$26–38/hr188 hourly ranges
Openings
Olive Jobs lists 13 open Clinical Research jobs in Tennessee and 1,460 across the US. 13% of them nationwide are listed as remote or flexible.
Hiring the most across the US
Experience
This posting asks for at least 2 years of experience; Clinical Research postings that state a minimum ask for 3 years at the median (1,082 postings).
Education
This posting asks for an associate degree; 606 of the 1,460 open Clinical Research jobs (42%) ask for an associate degree or higher.

Counted across the open, public US postings on Olive Jobs on November 11, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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