Medpace

Clinical Project Manager-Reference Laboratory

Medpace • $70K — $95K *
Cincinnati, OH 45238In-Person
Healthcare
Less than 5 years of experience
Reposted Today
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Job Overview by Ladders

Qualifications

  • Bachelor's degree in science or health-related field
  • 2-3 years of clinical laboratory experience
  • 2 years of project management experience
  • Knowledge of Microsoft Office
  • Excellent oral and written communication skills

Responsibilities

  • Supervise all aspects of designated clinical protocols
  • Create and maintain laboratory manuals and study-related documents
  • Develop and present clinical lab presentations at investigator meetings
  • Design specifications and monitor production of specimen collection kits
  • Serve as primary contact for Sponsors regarding assigned protocols
  • Track study status
  • Communicate all aspects of protocol to internal departments
  • Write, establish, and revise relevant Standard Operating Procedures

Benefits

  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local non-profits
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, eco-friendly campus with on-site fitness center
  • Structured career paths for professional growth
Full Job Description
Job Summary

We are currently seeking a Laboratory Project Manager for Medpace Reference Laboratories. This position is responsible for managing projects independently for one or more of Medpace Reference Laboratories' major clients.

Responsibilities

  • Supervise all aspects of designated clinical protocol with accountability of meeting agreed timelines, budgets, and performance quality;
  • Create and maintain laboratory manuals (general and study-specific) and other study- related documents;
  • Develop and present clinical laboratory presentations at investigator meetings;
  • Design specifications and monitor production of specimen collection kits;
  • Serve as primary contact for Sponsors regarding all aspects of assigned protocol(s);
  • Track study status as appropriate;
  • Communicate all aspects of protocol to various internal departments for appropriate study setup, maintenance, and closeout; and
  • Write, establish, and revise relevant Standard Operating Procedures and/or work instructions.


Qualifications

  • Bachelor's degree in science or a health-related field;
  • Knowledge of Microsoft Office;
  • 2 - 3 years of clinical laboratory experience;
  • 2 year project management experience required and;
  • Must have excellent oral and written communication skills

Travel: Up to 10%

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

About Medpace

Medpace is a clinical research organization that provides services to pharmaceutical, biotechnology, and medical device companies. The company's services include clinical trial management, regulatory consulting, and medical imaging. Medpace was founded in 1992 and is headquartered in Cincinnati, Ohio. The company has operations in North America, Europe, and Asia.
Learn more about Medpace
Size
4,700 employees
Market Cap
$6.4 billion
Industry
Pharmaceuticals & Biotech
Net Income
$145.3 million
Founded
1992
5 Year Trend
+22.1%
Revenue
$925.9 million
NASDAQ
MEDP
* Ladders Estimates

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