Clinical Research Coordinator

Southcoast Health • Fall River, MA

201d • $27 - $46 • Onsite

About The Position

Join Southcoast Health, where your future is as promising as the care we provide. Our commitment to each other, our patients, and our community is more than a mission - it's our way of life, and you'll be at the heart of it. Southcoast Health is a not-for-profit, charitable health system with multiple hospitals, clinics, and facilities throughout Southeastern Massachusetts and Rhode Island. Nestled in local communities, Southcoast Health provides inclusive, ethical workplaces where our highly skilled caregivers offer world-class, comprehensive healthcare close to home. Find out for yourself why Southcoast Health has been voted ‘Best Place to Work' for 7 years in a row! We are searching for a talented Clinical Research Coordinator.

Requirements

• Bachelor's Degree or equivalent experience is required.
• Degree in Healthcare administration, Healthcare, Science, or related field is preferred.
• Three to five years of experience working directly in clinical trials involving human subjects is preferred.
• Attention to detail and strong organizational skills are required.
• US Driver's license is required.
• Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), or Certified Clinical Research Associate (CCRA) is preferred.
• Certification within 6 months of hire is required if less than 2 years full-time clinical research experience.

Nice To Haves

• Experience in managing clinical trials.
• Strong communication skills.

Responsibilities

• Perform diversified duties in coordinating all activities related to clinical trials.
• Oversight of all research-related activities.
• Screening and evaluation of prospective trial patients.
• Clinical follow-up of enrolled trial patients.
• Correspondence and coordination with the Institutional Review Board and trial sponsors.
• Facilitation and development of relationships with Sponsors for clinical trials.
• Management/tracking of compliance with Federal and institution guidelines relating to conducting human subject research.
• Educate patients about clinical trials and obtain informed consent to participate.
• Responsible for implementing new trials.
• Collaborate with multiple MD Principal Investigators.
• Negotiate and maintain budgets.
• Manage audits and ensure adherence to study protocols regarding mandated visits, medicine management, and symptom tracking.

Benefits

• Competitive pay and comprehensive benefits package.
• Generous Earned Time Off Package.
• Employee Wellbeing Program.
• 403B Retirement Plan with company match.
• Tuition assistance / Federal Loan forgiveness programs.
• Professional growth opportunities and customized leadership training.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Hospitals
• Education Level: Bachelor's degree