WHY VITALIEF?
Vitalief, a fast-growing, innovative 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. We make a difference in people’s lives.
Our PEOPLE FIRST culture prioritizes personal and professional growth for all Vitalief employees. If you are interested in the clinical research profession and working with a team that respects and encourages your voice, then we want to speak with you!
WHAT IS THE ROLE?
Many clinical research teams struggle to retain resources to support numerous ongoing clinical trial activities. This continuing challenge negatively impacts the conduct and success of clinical trials. To address this problem, Vitalief is developing a Resource Optimization Center (ROC), an innovative partnering model that offers on-demand resources to our clients to ensure the continuity and success of their clinical trials. You will be a key member of our team and gain broad experience working in multiple clinical research centers, studying different disease groups within the client’s Oncology research program.
Under the direct supervision of a Clinical Research Manager at our client’s Clinical Research Center, you will be responsible for demonstrating your versatility and “can do” attitude, and adaptability in the following areas:
Work Locations: 100% on-site at one of our client’s New Jersey locations such as Hamilton, Toms River, Long Branch or Lakewood).
REQUIRED SKILLS:
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; inoculated annually for Influenza; and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.
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