Clinical Scientist - Remote US
About The Position
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 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.
Requirements
- 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
Nice To Haves
- Experience in oncology clinical research and/or oncology-focused laboratory-based research
- Familiarity with medical data review is preferred
Responsibilities
- 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
Benefits
- Comprehensive benefits to support physical, mental, and financial well-being
- Competitive compensation package
- Annual bonus or long-term incentive opportunities may be offered
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
