Junior Data Manager/Health Program Analyst

Company: Vitalief
Location: New Brunswick
Posted on: May 14, 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 role is 100% remote with up to 20% travel internationally Responsibilities:
  • Provide study coordination and data management oversight of specific protocols – including implementing and monitoring quality control SOPs, conducting periodic quality assurance monitoring, work with investigators to develop and implement protocols at our client's international sites.
  • Develop REDCap case report forms consistent with clinical protocols and investigator input, sets up SOPs for data collection sites to provide data capture (of clinical and laboratory data), and performs quality assurance audits to validate data in preparation for analysis by biostatisticians.
  • Maintains and manages research databases using Access and SAS software. Works with statisticians in creating the appropriate databases from collected data for analyses.
  • Monitors data quality per standard operating procedures for each protocol. Coordinate QA/QC with international on-site staff and Clients Study Coordinators. Required Skills:
    • Bachelor's degree in Public Health or related sciences required, advanced degree a plus.
    • One year of Research database experience.
    • 2 years biomedical research experience preferred.
    • Intermediate proficiency with statistical packages (SAS, R, MS Excel, MS Access, etc.).
    • Good understanding of clinical research components – data collection, human subjects protection, quality assurance and control.
    • Strong computer knowledge and graphic experience a plus.
    • Excellent communication, organization and presentation skills.
    • Ability to learn and integrate other related computer applications into existing operations. #LI-DNI Powered by JazzHR4O1118Lq2d

Keywords: Vitalief, New Brunswick , Junior Data Manager/Health Program Analyst, Executive , New Brunswick, New Jersey