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Southcoast Health · 3 hours ago

Clinical Research Coordinator-CV

US-MA-Fall River

Full-time

Onsite

Mid Level

3+ years exp

Southcoast Health is a not-for-profit health system dedicated to providing comprehensive healthcare in Southeastern Massachusetts and Rhode Island. They are seeking a Clinical Research Coordinator-CV to oversee clinical trials, manage compliance with guidelines, and educate patients on trial participation.

CommunitiesHealth CareNon Profit

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

Qualification

Clinical trials experienceCertified Clinical Research ProfessionalCertified Clinical Research CoordinatorCertified Clinical Research AssociateHealthcare administration degreeAttention to detailOrganizational skills

Required

Bachelors Degree or the equivalent experience is required

Attention to detail and strong organizational skills are required

US Drivers license is required

Certification within 6 months of hire

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

Preferred

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