Study Manager
Listed on 2026-01-16
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Research/Development
Clinical Research -
Healthcare
Clinical Research
Join to apply for the Study Manager role at Vita Global Sciences, a Kelly Company
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$54.81/hr - $54.81/hr
Kelly Science and Clinical FSP is currently seeking a Study Manager for a long‑term engagement with one of our Global Pharmaceutical clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full‑time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K (no match) and a variety of other benefits to choose from.
You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
- Assists the SM Study Lead and study team with the operational conduct of clinical studies (e.g., CTT minutes, clinical supplies planning/tracking, lab specimen tracking, imaging data reconciliation, status update reports, study closeout activities)
- May support a single study or multiple studies
- May lead a study with limited scope (e.g., Survival Follow-up)
- May be responsible for tracking study timelines and will be proficient in project management tools
- May interact with internal and external stakeholders (study sites, vendors, committees, etc.) in support of clinical study objectives
- At least 2 year Pharmaceutical and/or clinical drug development experience (such as pharmaceutical/biopharma companies, hospital settings, research sites, clinical trial units, CRO, SMO) in the last 5 years required
- TA-specific experience beneficial
One Note experience preferred.
- BS/BA/MS/PhD
Applicants must be currently authorized to work in the US on a full‑time basis now and in the future.
Posted By:
Karli Minor
Mid‑Senior level
Employment TypeContract
Job FunctionResearch, Analyst, and Information Technology
IndustriesBusiness Consulting and Services
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