Clinical Scientist - Remote US

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.

Our Clinical Scientist is primarily responsible for providing scientific assistance and support for the Sarah Cannon Medical Directors and study teams who oversee trials conducted by SCRI. Your key responsibilities will include providing clinical, therapeutic and scientific expertise to the study team, supporting the creation of trial deliverables, and ongoing medical data review with a specific focus on patient safety and efficacy to ensure that the data is coherent, complete, and accurate so that it is suitable to meet study deliverables. You will follow standard operating procedures, ICH-GCP, and all applicable regulatory requirements.

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

Duties include and are not limited to:

• Serve as the scientific point of contact for the study team on both industry-sponsored and investigator-initiated trials

• Collaborate with medical writing during the development of clinical study protocols and attend protocol development meetings

• Perform medical and scientific review of clinical study protocols, informed consent forms, investigator brochures, case report forms, clinical study reports, TFL shells, TFLs, and other study documentations and publications

• Perform medical data review and assessments of safety and efficacy data

• Scientifically review clinical research data including patient demographics, medical and disease history, concomitant medications, laboratory values, adverse events, disease response verification, and overall review to enhance data quality

• Other duties as assigned

Qualifications needed include:

• Bachelor’s Degree (4-year program) required

• Minimum 2+ years of experience analyzing data and science in clinical research and/or laboratory-based research or within the pharmaceutical or CRO environment

• Prior work experience in a highly-detailed role such as nursing or scientific research

• Prior work experience in a collaborative environment taking initiatives when needed such as process improvement

Preferred Experience includes:

• Experience in oncology clinical research and/or oncology-focused laboratory-based research

• Familiarity with medical data review is 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.

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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.