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Regional Study Coordinator (1-year contract)Labcorp • Harrogate, England, GB
Regional Study Coordinator (1-year contract)

Regional Study Coordinator (1-year contract)

Labcorp • Harrogate, England, GB
30+ days ago
Job type
  • Full-time
Job description

Regional Study Coordinator (1-year contract)

Labcorp Harrogate, England, United Kingdom

Get ready to redefine what’s possible and discover your extraordinary potential. Here at Labcorp Drug Development, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.

Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.

The Company - LabCorp Drug Development

As one of the world's largest and most comprehensive drug development services companies, LabCorp Drug Development has helped pharmaceutical and biotech companies develop one-third of the all prescription drugs in the marketplace today.

The Position - 1 year contract

This position falls within our Central Labs Services group supporting Central Labs Projects for clinical trials phases I-IV. This position is remotely based.

Do you excel at coordinating events and information into a complex timeline? If you have a background in science or experience in project management, then joining our study team as a Temporary Regional Study Coordinator (RSC), an associate project manager role, could be the gateway to unleash your extraordinary potential with a career in project management.

Our RSCs manage local laboratory operations and serve as the bridge between our internal departments and various clinical studies. To be successful, RSCs must manage many competing interests, and communicate and articulate critical information to each department and amongst the project management team.

About The Job

You’ll join our Global Project Management Department, a team of exceptional people who are unified by an energizing purpose to transform healthcare and improve lives around the globe. Clinical studies are developed and managed collaboratively by a study team, and the RSC manages the day-to-day activities of a clinical trial at a regional level. RSCs manage multiple studies and the responsibilities for each include:

  • Collaborate with the Global Study Manager for all local study related aspects. Specifically, study set up and closure; ordering of study start up supplies, answering CRA questions regarding country specific regulations, etc.
  • Act as regional liaison between Global Study Manager and various CLS departments involved in the study.
  • Act as a regional liaison between assigned client representatives (e.g., CRAs or Site Monitors) and Covance CLS internal departments and teams.
  • Monitor, track and provide resolution to all local study issues; especially logistic issues and/or delays in receipt of study supplies, while keeping the Global Study Manager in the communication loop.
  • Clean the laboratory database; determine why a lab sample placed on hold is not being analyzed, resolve the issue.
  • Deliver outstanding customer service and timely responsiveness to ensure client satisfaction, which requires a clear understanding of study design and major budget drivers.
  • Work in a matrix environment where some task assignments are channeled to RSCs while others are delegated to other functional groups.

Your Skills

  • Excellent communication and organization skills
  • Demonstrated time management skills
  • Dedicated to teamwork
  • Ability to plan and prioritize
  • Thrive in a fast-paced environment
  • Fluency in English at a work-proficiency level

Requirements

  • A bachelor’s degree and customer service experience. A university degree in science is preferred, but not required if you have demonstrated project management experience.
  • First experience in client facing role and/or project management
  • Good understanding of Central Lab Services or clinical research/studies
  • To help you reach your Labcorp Potential, we provide a robust training program followed by structured mentorship, as well as continued support via independent and digital learning programs. You will have opportunities for advancement and be a part of a community of hard-working people who push new boundaries together.

Thrive personally and professionally at Labcorp Drug Development

Working at Labcorp Drug Development, you’ll continue to grow in our learning-based culture so you’ll know how to expertly respond and adapt as the industry continues to evolve. Here, you’ll put your education to work as you play a meaningful role in advancing healthcare and making a difference in people’s lives. Labcorp Drug Development offers great benefits, global experience and the opportunity to work independently within a team-oriented environment.

Get to know Labcorp Drug Development

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our diagnostics and drug development capabilities, we provide insights and accelerate innovations that empower patients and providers and help medical, biotech, and pharmaceutical companies transform ideas into innovations.

Here, you can join our more than 75,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives.

Labcorp Is Proud To Be An Equal Opportunity Employer

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination. Qualified applicants will receive consideration without regard to race, religion, color, national origin, sex, family or parental status, marital status, sexual orientation, gender identity, age, veteran status, disability, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

Seniority level

  • Entry level

Employment type

  • Full-time

Job function

  • Research, Analyst, and Information Technology

Industries

  • Hospitals and Health Care

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