Sarah Cannon Research Institute (SCRI) is hiring a Clinical Safety Coordinator to serve as the primary Pharmacovigilance contact for our Investigator Initiated and Research Collaboration Trials. At SCRI, people living with cancer are at the heart of every decision we make. You'll join a mission-driven team transforming care through clinical excellence and research.
What You'll Do
- Accountable for the delivery of a Safety Monitoring Plan for assigned trials, describing the end-to-end safety reporting process.
- Ensure compliance with study protocols, Funding Partner requirements, and applicable Pharmacovigilance regulations.
- Prepare expedited individual safety reports and ensure their further submission via regulatory functions.
- Perform proficient data entry of safety case reports into the ARGUS safety database.
- Review safety case reports to confirm ARGUS safety database entries are complete and accurate.
What We're Looking For
- Work experience with all Microsoft Office products, including Excel, and varying software applications or databases.
Nice to Have
- A Bachelor's Degree is preferred; relevant experience may be substituted for education.
- 3+ years of Data Entry experience in a hospital, medical office, or research environment requiring a high level of attention to detail.
- Proven ability to appropriately manage and prioritize assigned tasks and adhere to specific deadlines.
Technical Stack
- Microsoft Office Suite, including Excel
- ARGUS safety database
Benefits & Compensation
- We offer a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being.
Work Mode
This is a fully remote position open to candidates located anywhere within the United States.
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.
