Clinical Project Associate Job at Sarah Cannon Research Institute, USA | Apply Now For Remote Job
A rare chance has emerged for aspiring candidates to join the Sarah Cannon Research Institute (SCRI). This Clinical Project Associate Job is fully remote and offers candidates the opportunity to contribute to innovative oncology treatments while working from anywhere in the United States. Interested applicants should apply soon, as this role is essential in advancing cancer care.
- Job Position: Clinical Project Associate
- Location: Fully Remote, USA, TN
- Job Requisition ID: JR0151251
About The 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.
Clinical Project Associate Job Description
In this Clinical Project Associate Job, the selected candidate will be responsible for ensuring the Trial Master File (TMF) is set up and maintained in “audit ready” condition. This includes conducting 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. The Clinical Project Associate will maintain clinical trial management systems and tracking tools while actively participating in cross-functional teams to ensure delivery of project deliverables.
Key Responsibilities
- Set up and 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 specialists 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 liaising with Clinical Research Associates and investigative sites to resolve outstanding regulatory issues.
- Review study documents to ensure they are current, complete, and accurate.
- Other duties as assigned.
Eligibility Criteria
- 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.
Documents Required
- Resume/CV.
- Cover letter (if applicable).
- References (if applicable).
This Clinical Project Associate Job at the Sarah Cannon Research Institute allows qualified candidates to play a vital role in advancing cancer research and treatment. Interested individuals are encouraged to apply through the official listing while the role remains open.
