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 a rewarding career path in the clinical research profession and working with a team that respects and encourages your voice, then we want to speak with you!

Work Location: This role is currently 100% on-site in New Brunswick, NJ, which potential occasional travel locally to client sites in New Jersey.

Responsibilities:

• The Clinical Research Education and Training Coordinator is responsible for supporting the educational growth and development of a diverse group of research personnel who support clinical research conducted at the client site.
• Develops, implements, and continually updates and educational programs, curricula, courses, and learning materials for clinical research personnel.
• Conducts onboarding and orientation of clinical research personnel. Trains new clinical research personnel to independently manage complex phase I-III clinical trials, including items such as Patient Consenting, Screening, Enrolling participants after ensuring eligibility, Managing participant treatment per protocol, Collecting and reporting research data, Reporting Serious Adverse Events and Deviations per protocol, Ensuring adherence to protocol requirements.
• Assists with evaluating training needs of existing personnel to identify knowledge gaps.
• Maintains orientation and training system and materials.
• Identifies areas for performance improvement and engages research personnel in improvement projects.
• Maintains up-to-date knowledge and adheres to policies, procedures, guidance, and practice standards set forth by the client, FDA, and all regulatory bodies.
• Adheres to all pertinent federal, state, and client regulations, laws, and policies as they presently exist and as they change or are modified.

Required Skills:

• Bachelor’s Degree required plus 3 to 5 years of clinical research experience.
• At least one (1) year of formalized and structured training or educator experience.
• Working knowledge of the Title 21 Code of Federal Regulations (CFR), International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) Guidelines
• Oncology experience preferred.
• ACRP or SOCRA certification preferred.
• Positions requires critical thinking skills, decisive judgment, and working with minimum supervision.
• Demonstrates excellent interpersonal skills, able to establish rapport with a wide range of people, able to work in a stressful environment, and able to work on multiple tasks.
• Demonstrates excellent organizational skills and is detail oriented.
• Proficient in computer applications (MS Office Suite: Word, Excel, PowerPoint, and Microsoft Teams).
• Must be willing to travel locally to client sites in New Jersey.

PHYSICAL DEMANDS: Standing, sitting, walking, talking, and hearing. No special vision requirements. Lifting up to 25lbs.

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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