Clinical Research Coordinator

Found in: Jooble CA O C2 - 6 days ago

NouveauBrunswick, Canada Vitalief Full time

If you are interested a rewarding career path in the clinical research profession, a healthier “Life” work balance, and working with a team that respects and encourages your voice, then we want to speak with you
Vitalief, a fast-growing, “best of breed” Research and Clinical Trial Solutions Company, is committed to identifying talented and passionate clinical research professionals to join our exceptional team and support our clients in planning and executing successful clinical trials.
Investment in your career progression
~ 20 PTO (Paid Time Off) days plus 9 paid Holidays annually
~ Company paid life insurance and short / long term disability coverage; 401K retirement program; Robust healthcare plans to choose from

Work Location: Work is 100% on-site in New Brunswick, NJ.
Under the direct supervision of the Nurse Manager of Clinical Research Center, performs subject recruitment, consenting, data entry, and other clinical trial activities for several trials.
Serves as a liaison between the organization, investigators, members of the research team (i.e., physicians, nurses, hospital, and laboratory staff), and the research sponsors – to ensure that services are coordinated and delivered to patients in a timely manner.
Manages eligibility check lists, perform patient screening/consenting (informed consent), patient enrollment activation (based on clinical trial agreement and investigator discretion) and managing patient care (patient retention).
Maintains research record (e.g., for all patients enrolled in clinical trials.
Participates in site preparation for trials including: protocol feasibility, preliminary study budget, startup meeting preparation, training staff, and preparation of IRB applications and preparation of regulatory documents, study documents and forms.
Assists patients in understanding their diagnosis, treatment options, and the resources available including educating eligible patients about appropriate clinical research studies and technologies.
Oversees specimen processing for analysis and/or shipment, and documents laboratory results.
Minimum of 1 or more years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; regulatory compliance and data management.
Bachelor’s Degree required.
Demonstrated experience working on multiple clinical trials concurrently.
physicians, nurses, hospital, and laboratory staff) to ensure that services are coordinated and delivered to patients in a timely manner.
Demonstrated computer skills with Microsoft Office applications.
Any exposure EPIC (Electronic Health Records system) and/or OnCore (Clinical Trials Management System) is a plus.
IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that requires all on-site resources such as prospective Vitalief consultants to provide proof that they are fully vaccinated for Covid-19;

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