Study Manager

Vita Global Sciences, a Kelly Company; Rahway (NJ); On-site; USD 62,292 - 88,719; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401K options

Paid time off

Job summary

A global pharmaceutical service provider is looking for a Study Manager in Rahway, NJ. This full-time, contract role requires at least 2 years of experience in pharmaceutical and clinical drug development. The candidate will assist in operational conduct of studies, manage timelines, and communicate with stakeholders. Proficiency in Microsoft Office is essential. This opportunity offers competitive pay and full benefits, including medical, dental, and 401K options.

Qualifications

• At least 2 years of experience in Pharmaceutical and/or clinical drug development in the last 5 years.
• TA-specific experience beneficial.

Responsibilities

• Assist the SM Study Lead and study team with operational conduct of clinical studies.
• Support a single or multiple studies and track study timelines.
• Interact with stakeholders to support clinical study objectives.

Skills

Pharmaceutical and/or clinical drug development experience

Oral and written communication skills

Proficiency in Microsoft Office

Project management tools proficiency

Education

BS/BA/MS/PhD

Tools

Microsoft Office (Outlook, Word, Excel, PowerPoint)

OneNote

Job description

Join to apply for the Study Manager role at Vita Global Sciences, a Kelly Company.

Base pay range

$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.

Description of Services

• 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

Minimum Years of Experience

• 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

Demonstrated oral and written communication skills

Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required; OneNote experience preferred.

Educational Requirements

• 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

Seniority Level

Mid‑Senior level

Employment Type

Contract

Job Function

Research, Analyst, and Information Technology

Industries

Business Consulting and Services