Clinical Research Job at Bon Secours Mercy Health, USA | Life Sciences | Apply Now
If you are an experienced clinical trials professional looking to step into a specialized oncology research role, this full-time position at Bon Secours Mercy Health is an exceptional opportunity. Located at the Richmond Cancer Institute within St. Francis Medical Center in Midlothian, Virginia, this on-site role embeds you directly within an advanced ancillary support service line. For detail-oriented coordinators searching for a high-impact Clinical Research Job, this position offers a structured platform to manage institutional review board (IRB) filings, patient data integrity, and cross-departmental operations. It serves as an elite launchpad for a long-term oncology administration pathway and stands out as a premier Clinical Research Coordinator Job for professionals seeking a rewarding Life Sciences Job in the healthcare sector.
- Job Position: Clinical Research Coordinator – Cancer Institute at St. Francis Medical Center
- Req ID: R270064
- Location: 13710 St Francis Blvd, Midlothian, VA 23114, United States of America
About The Company
Bon Secours Mercy Health is a major, mission-driven healthcare system dedicated to improving the health and well-being of its communities while supporting its associates personally and professionally. The Richmond Cancer Institute Medical Oncology team at St. Francis Medical Center operates at the leading edge of oncology diagnostics and therapeutics. By joining this specialized team, you help advance breakthrough clinical trials that directly impact patient survival rates, bringing innovative cancer therapies from scientific discovery to real-world patient care.
Clinical Research Job – Key Responsibilities
As a Clinical Research Coordinator, you will manage the administrative, data, and regulatory lifecycles of active clinical research trials, ensuring absolute compliance with ethical guidelines and sponsor timelines.
Your core operational, documentation, and compliance duties will include:
- Trial Start-Up & Collaboration: Interacting directly with legal, finance, and compliance departments to facilitate the rapid launch, contract processing, and operational setup of new clinical trials.
- Patient Consent Management: Handling patient informed consent documentation and study participation agreements in strict accordance with ethical trial frameworks to advance this Clinical Research Coordinator Job.
- Data Capture & Entry: Capturing comprehensive patient clinical data and inputting it accurately into confidential electronic data management systems provided by industry pharmaceutical sponsors.
- IRB Regulatory Submissions: Preparing and managing complete Institutional Review Board (IRB) submissions for new protocols, study amendments, and mandatory annual continuing reviews.
- Safety & SAE Reporting: Reviewing safety alerts and submitting urgent Serious Adverse Event (SAE) documentation to the IRB and sponsors within required compliance windows.
- Document Auditing & Support: Maintaining comprehensive regulatory files, tracking critical protocol deadlines, and assisting with overall departmental needs in a flexible, backup capacity for this Clinical Research Job.
Qualifications & Profile Requirements For Clinical Research Job
This intermediate coordination vacancy is tailored for highly organized candidates who understand the strict regulatory demands of human subjects research.
Required Criteria:
- Educational Foundation: A Bachelor’s degree in a life science, or related quantitative scientific field is mandatory for this Life Sciences Job.
- Experience Track: A minimum of 2 years of direct experience working in clinical research operations or regulatory affairs.
- Compliance Knowledge: Proven familiarity with the ethical and regulatory requirements of human subjects research, including IRB protocols, FDA mandates, and ICH-GCP guidelines.
- Technical Software Skills: High proficiency with Microsoft Office applications and a strong familiarity operating within regulatory databases.
- Core Competencies: Exceptional attention to detail, robust organizational habits, critical thinking skills, and excellent written and verbal communication styles.
Preferred Assets:
- A Master’s degree in a health-scientific discipline or an active professional regulatory certification (e.g., CCRC via ACRP or CCRP via SOCRA).
- Prior clinical coordination experience working within an academic medical center or a large, multi-site research institution.
- Hands-on knowledge working with electronic regulatory systems and advanced Clinical Trial Management Systems (such as OnCore or REDCap).
In short, the Clinical Research Coordinator position at St. Francis Medical Center is a definitive route to transitioning your foundational life sciences background into a high-visibility career in oncology trial operations. Securing this role allows you to bypass generalized laboratory benchwork and take complete operational ownership of regulatory files, clinical datasets, and safety reports that determine the safety of next-generation cancer therapies. If you live in the Richmond, VA area, possess two years of clinical tracking experience, and want to align with a mission-driven organization, apply today to secure this premier Clinical Research Coordinator Job.
