Clinical Research Coordinator, Cardiovascular Device Clinical Trials

Southcoast Health System•Fall River, MA

1d•$57,554 - $96,762•Onsite

About The Position

Join Southcoast Health, a not-for-profit, charitable health system with multiple hospitals, clinics, and facilities throughout Southeastern Massachusetts and Rhode Island. We are searching for a talented Clinical Research Coordinator to join our team. Southcoast Health offers a culture of well-being, competitive pay, comprehensive benefits, generous Earned Time Off, an Employee Wellbeing Program, a 403B Retirement Plan with company match, and tuition assistance/Federal Loan Forgiveness programs. We are committed to inclusive, ethical workplaces where highly skilled caregivers offer world-class, comprehensive healthcare close to home.

Requirements

Bachelors Degree or the equivalent experience is required.
Attention to detail and strong organizational skills are required.
US Drivers license is 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.

Nice To Haves

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.
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.

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 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.