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Program Support Coordinator / Project Manager

Company: Vitalief
Location: New Brunswick
Posted on: May 8, 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:
    • Handling and producing a large volume of oncology clinical trials information to assist with fulfilling Disease Specific Group (DSG) expectations as outlined by policy and aligning with client expectations.
    • Analyzing key performance metrics, providing analysis to leadership via business intelligence, and assistance in preparation of data as needed for grant reporting and competitive renewal requirements.
    • Assists DSG Leaders with creating and managing portfolio maps to support the vetting and prioritizing of new trials in support of ongoing DSG study portfolio review and management.
    • Assists in preparation of reports, presentations, and other documentation in the ongoing oversight of programmatic activities and in the investigation and development of solutions to problem areas.
    • Supports investigators with SRB submissions and Study Interest Forms of new protocols. Tracking and updating process in OnCoreĀ®.
    • Liaise with Study Activation Coordinators and Regulatory staff regarding the status of studies in the start-up process to support timely activation of new Oncology studies.
    • Collects data relevant to DSG programmatic activities and processes on a regular basis from various stakeholders. Develops and maintains DSG reports and analytics to support Cancer Center Support Grant (CCSG) activities. Required Skills:
      • Bachelor's Degree.
      • Three (3) years professional experience with planning, coordinating, evaluating and managing of projects/program; developing strong action plans; and researching and interpreting data required.
      • One (1) to three (3) years of clinical research experience preferred.
      • Computer literacy with proficiency and working knowledge of database and reporting tools such as Microsoft Word, Excel, Access and PowerPoint.
      • Able to run disease group meetings, delegate, take meeting minutes and follow up.
      • Effective oral and written communication skills.
      • Excellent organizational skills and attention to detail.#LI-DNIPowered by JazzHR8hIBMJB56u

Keywords: Vitalief, New Brunswick , Program Support Coordinator / Project Manager, Executive , New Brunswick, New Jersey

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