Study Coordinator-Project Manager at Powered Research
RTP, NC 27709, USA -
Full Time


Start Date

Immediate

Expiry Date

05 Dec, 25

Salary

75000.0

Posted On

06 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Health Insurance, Drug Discovery, Oncology, Ophthalmology, Smartsheet, Life Sciences, Pharmacology, Ms Project

Industry

Information Technology/IT

Description

QUALIFICATIONS:

  • Bachelor’s or advanced degree in life sciences, pharmacology, ophthalmology, oncology, or related field.
  • 3+ years of project management experience in a CRO or preclinical research setting.
  • Experience managing sponsor relationships and multi-study portfolios.
  • PMP certification or equivalent is a plus.

SKILLS & ATTRIBUTES

  • Excellent communication and internal client-facing skills.
  • Strong organizational and multitasking abilities.
  • Strong working knowledge of drug discovery and development
  • Proficiency in project tracking tools (e.g., MS Project, Smartsheet, or similar).
  • Collaborative, detail-oriented, and solutions-driven mindset.
    Job Type: Full-time
    Pay: $75,000.00 - $100,000.00 per year

Benefits:

  • 401(k)
  • Health insurance
  • Paid time off

Work Location: In perso

Responsibilities

ROLE OVERVIEW

As a Project Manager / Study Coordinator at this leading CRO specializing in ophthalmology studies, you will oversee the planning, execution, and delivery of sponsor-driven preclinical projects. You’ll serve as the primary liaison between the study director and the preclinical team, ensuring scientific rigor, operational excellence, and timely execution of studies.

KEY RESPONSIBILITIES

  • Engagement: Act as the main liaison between study directors and internal study teams. Translate sponsor objectives into executable study plans with the guidance of the Principal Investigator / Study Director.
  • Project Proposal Development: Study Outline development and costing assigned projects
  • IACUC protocol development: In cooperation with the Study Director
  • Timeline & Milestone Management: Develop, schedule and track project timelines, deliverables, and resource allocation across multiple concurrent studies.
  • CRO Operations: Coordinate study activities with cross-functional teams (animal technicians, pharmacologists, imaging scientists, data analysts).
  • Documentation: Ensure Guideline and SOP compliance, assess study documentation, and support data verification, GLP experience a plus
  • Risk & Issue Management: Identify operational risks and proactively suggest mitigation strategies.
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