Clinical Project Associate

McKesson’s Corporate; Tennessee; Hybrid; USD 55,000 - 90,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a detail-oriented professional to manage TMF/documentation for clinical trials. This remote US role emphasizes audit readiness and cross-functional collaboration with the clinical operations team.

Ideal candidates have at least 1 year of clinical research experience (oncology preferred) and a high school diploma. The position offers remote work with standard benefits and career development opportunities within SCRI’s oncology

Qualifications

• Minimum High School Diploma or GED.
• 1 year of clinical research experience required; 3 years preferred.
• Oncology clinical research experience preferred.

Responsibilities

• Set up and maintain the Trial Master File (TMF) in audit-ready condition throughout the study lifecycle.
• Maintain clinical trial management systems and tracking tools across cross-functional teams.
• Set up, document collection, and upload files to the TMF/eTMF; perform quality review of documents.

Skills

Clinical research

Oncology

Documentation management

Education

High School Diploma or GED

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.

Responsibilities

• Ensure the Trial Master File (TMF) is set-up and maintained in “audit ready” condition; and conduct critical documentation collection and review throughout the lifecycle of the study, in accordance with Good Clinical Practices, ICH Guidelines, Federal Regulations and Development Innovations SOPs.
• Maintain clinical trial management systems and tracking tools, actively participating in cross-functional teams to ensure delivery of project deliverables.
• Set-up, document collection/upload of files to the TMF/eTMF.
• Perform initial quality review of documents prior to upload/filing in the TMF/eTMF.
• Partner with document specialist to maintain the Trial Master File (TMF) in “audit ready” condition from study start to completion.
• Assist with confirming the qualifications of investigators and investigative sites throughout the conduct of the clinical trial.
• Perform critical document distribution to and collection from the investigative sites throughout the lifecycle of the clinical trial.
• Proactively liaise with Clinical Research Associate and investigative site to resolve outstanding regulatory issues.
• Review study documents to ensure they are current, complete and accurate.
• Other duties as assigned.

This position is remote based in the US; relocation assistance and visa sponsorship are not available.

Qualifications

• Minimum High School Diploma or GED
• At least 1 year of clinical research experience required; at least 3 years of clinical research experience preferred.
• Oncology clinical research 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.

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. 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.

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.