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Junior Clinical Research Associate

Company: Vitalief
Location: New Brunswick
Posted on: May 9, 2022

Job Description:

Job DescriptionWhy Vitalief? A fast-growing, innovative Clinical Trial Solutions Company, Vitalief is committed to identifying talented and passionate clinical research professionals to join our exceptional team as experts and active members of our clients' research efforts.We pride ourselves in fostering a culture of "people first" by hiring and retaining clinical research professionals as employees of Vitalief. We are a company that prioritizes personal and professional growth for OUR team. Although unconventional, we believe this to be the right approach and that our culture will attract and retain exceptional clinical research talent. None of this is possible without the drive and passion of our Vitalief team members. If you are interested in the clinical research profession and being part of a culture that includes:

  • The ability to have a voice challenging the status quo with novel thinking
  • Flexible work environment
  • Transparent Leadership
  • Investment in your career progression
  • Variable incentive/reward system
  • Encouraged and mentored by the talented Vitalief team to achieve full potential Then we want to speak with you!Note: This position is 100% remote, however the resource needs to reside in the EST Zone. Responsibilities:
    • Under the direction of the Principal Investigator(s), Data and Operations Management Director, and other leadership, the Senior Research Coordinator is responsible for on-site and off-site study coordination and data management oversight of specific assigned scientific protocol(s).
      • Implementing and monitoring quality control SOPs, conducting periodic monitoring visits, and working with investigators at the sites to develop and implement protocols.
      • Coordinates and administers protocols and translates protocols into operational implementation and conduct at the foreign and domestic sites. Site locations include, but are not limited to: North America, Peru, Brazil, Moldova, Uganda, Kenya, South Africa, India, Vietnam, Indonesia, China, and the Philippines.
      • Participates in the development of performance standards, selection of methodology and instrumentation and coordination of the analytical, biochemical, physiology and instrumentation functions with the clinical and research areas to ensure conformance with the goals and objectives of the department.
      • Assists faculty in developing study patient consent forms & applications to the IRB. Responsible for reporting protocol changes to the IRB.
      • Provides specialized protocol, procedure and application (REDCap, FreezerPro specimen tracking) training to international site study team (investigators and staff).
      • Assures timely responses to study inquiries and schedules regular "monitoring" visits. Coordinates quality assurance/quality control activities with on-site staff and investigators. Required Skills:
        • Bachelor's Degree plus three (3) years of scientific/clinical research experience OR Master's Degree plus two (2) years of scientific/clinical research experience.
        • Ability to travel 6 weeks yearly – consisting of three 2-week trips to either South America, Africa and/or Asia.
        • Strong relationship building and interpersonal skills.
        • Computer literacy with proficiency and working knowledge of database and reporting tools such as Microsoft Word, Excel, Access and PowerPoint.
        • Effective oral and written communication skills.
        • Excellent organizational skills and attention to detail.#LI-DNIPowered by JazzHRuH4fRpHZbx

Keywords: Vitalief, New Brunswick , Junior Clinical Research Associate, Healthcare , New Brunswick, New Jersey

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