Eurofins Lancaster Laboratories

Clinical Project Manager

Eurofins Lancaster Laboratories • $95K — $115K *
Lancaster, PA 17603In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
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Job Overview by Ladders

Qualifications

  • Bachelor's degree in healthcare/life sciences or equivalent industry experience (5+ years) in Central Lab.
  • 2-4 years of Project Management experience in complex project service industries.
  • 2-4 years of relevant clinical project experience with a CRO or Sponsor organization.
  • Authorization to work in the United States indefinitely without restriction or sponsorship.
  • Fluent in English; knowledge of other languages is advantageous.

Responsibilities

  • Oversee project execution and ensure proactive communication with clients.
  • Ensure timely and efficient study execution according to protocol within the regional scope.
  • Maintain compliance with global project management standards and procedures.
  • Obtain client approval on specifications before production.
  • Manage project timelines, budgets, and implement corrective actions as necessary.
  • Maintain an accurate and complete Study File for regulatory inspections.
  • Support sales efforts in the bid process for new and repeat business.

Benefits

  • Comprehensive medical coverage, dental, and vision options.
  • Life and disability insurance.
  • 401(k) with company match.
  • Paid vacation and holidays.
Full Job Description
Job Description

Lead and/or support regional teams in the execution of projects and to excel in service performance and
delivery. To deliver superior performance (time, quality, cost, and service) to exceed the clients' expectations
and specifications and continued business relationship.

Project Manager Duties Include but are not Limited to the Following:
  • Oversee project conduct to provide a pro-active and timely project/study communication with the clients to maximize client satisfaction and continuing relationships as the primary point of contact between the Clinical team and ECL
  • Ensure accurate, timely and efficient study execution according to clinical protocol/quote within the regional scope of the project
  • Ensure that the project is conducted in accordance with project management global standards and procedures of ECL
  • Ensure that client's formal approval on specifications, incl. amendments, are obtained before putting into production
  • Ensure all study activities (set-up, conduct, closure) are delivered on-time, in full (on specs) and within budgets and oversee corrective actions to bring them back on track and expectations
  • Maintain complete financial management of the budget for assigned studies
  • Take appropriate actions and escalate to/follow-through with Head PM, other functional and site leaders if services and projects deviate from expectations
  • Ensure that the Study File is accurate, maintained, complete, and self-explanatory such that it will pass a regulatory inspection during the life time of the study, and at any time after closure in line with the prevailing regulations at the time of the study
  • When required, actively support sales in bid process to gain repeat, and/or new, long-term business
  • Support and work with QA, be present during the study audit, and present the study file
  • Ensure timely resolution of corrective actions assigned to the Project Manager
  • Execute projects within timelines and on budget
  • Lead, manage, and support assigned projects to surpass global standards in a competitive and fluid drug development services business environment
  • Senior Project Managers will support Global Project Managers on global studies in their region
  • Perform other duties assigned my manager


Qualifications

Basic Minimum Education Qualifications:
  • Project Manager:
    • A Bachelor degree in healthcare/life sciences (laboratory or clinical services preferred) or significant industry experience (5+ years) in Central Lab is also considered acceptable.

Basic Minimum Work Requirements:
  • Project Manager:
    • Minimum of 2 - 4 years Project Management experience in complex project service industries
    • Minimum of 2 - 4 years relevant clinical project experience with a CRO or Sponsor organization
  • Authorization to work in the United States indefinitely without restriction or sponsorship.

The Ideal Candidate Possesses the Following:
  • Energetic and enthusiastic person, willing to travel as required to attend investigator meetings, other necessary client meetings, and internal global meetings.
  • Fuent in English, other languages of operating sites and global clients of advantage
  • A proven track record of strong customer focus, driven by quality and exceptional level of service
  • Possess excellent communication skills, with the ability to assimilate and rationalize large volumes of information and determine best course of action.
  • Excellent communication skills being to assimilate large volumes of information and requests to determine the best course of action
  • Good organizational and analytical skills, client service focus and performance orientation


Additional Information

Position is full-time working remotely Monday - Friday, 8:00am - 5:00pm, and additional hours as needed.
  • Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

About Eurofins Lancaster Laboratories

Eurofins Lancaster Laboratories is a leading contract research organization (CRO) providing analytical, research and testing services to clients in the pharmaceutical, biopharmaceutical, biotechnology, crop protection, chemical, food, environmental and consumer products industries. The company was founded in 1961 and has grown to become one of the largest CROs in the world, with over 50 locations in 20 countries. Eurofins Lancaster Laboratories is part of the Eurofins Scientific Group, a global leader in bioanalytical testing and laboratory services. The company's services include method development and validation, stability testing, quality control testing, and regulatory compliance support.
Learn more about Eurofins Lancaster Laboratories
Size
12,000 employees
Industry
Pharmaceuticals & Biotech
* Ladders Estimates

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