Clinical Research Coordinator-CV at Southcoast Health System, Inc.

Fall River, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

16 May, 26

Salary

96761.6

Posted On

15 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trials Coordination, Patient Screening, Clinical Follow-up, Institutional Review Board Correspondence, Sponsor Coordination, Compliance Management, Informed Consent, Protocol Adherence, Budget Negotiation, Audit Management, Medicine Management, Symptom Tracking, Attention to Detail, Organizational Skills

Industry

Hospitals and Health Care

Description

Overview Community Focused. Care Driven. 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-CV This is an onsite role A career at Southcoast Health offers you: A culture of well-being that embraces, respects, and celebrates the rich diversity of one another and the communities we serve 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 **Available to regular status employees who are scheduled to work a minimum of 24 hours. Southcoast Health is an Equal Opportunity Employer. Responsibilities Under the direction of the Care Center Director or Designee, perform diversified duties in coordinating all activities related to clinical trials. Duties include but are not limited to 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 to clinical trials and obtain informed consent to participate. Responsible for implementing new trials, collaborating with multiple MD Principal Investigators, negotiating and maintaining budgets, managing audits and ensuring adherence to study protocols about mandated visits, medicine management and symptom tracking. Qualifications Bachelors Degree or the 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 Drivers 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. If less than 2 years full time clinical research experience, the minimum allowed before you can sit for the exam, certification will then be required. Must be fully vaccinated against seasonal Influenza and the COVID 19 virus or to be exempt from the requirement for medical or personal reasons by signing a statement certifying you are choosing to be exempt from vaccination once hired Compensation: Pay rate will be determined based on level of experience. Pay Range USD $57,553.60 - USD $96,761.60 /Yr. Rotation Schedule Requirement M-F

Responsibilities

The coordinator will perform diversified duties in overseeing all activities related to clinical trials, including screening prospective patients, managing clinical follow-up, and handling correspondence with the IRB and trial sponsors. Responsibilities also involve implementing new trials, collaborating with Principal Investigators, negotiating budgets, and ensuring adherence to study protocols.