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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