Skip to main content

This job has expired

Associate Project Coordinator

Employer
Labcorp
Location
Leeds, United Kingdom
Salary
Competitive
Start date
12 Jun 2021
Closing date
7 Jul 2021

View more

Discipline
Project Management
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details


Your new employer is Labcorp Drug Development , the world's most comprehensive drug development company, dedicated to improving health and improving lives. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow's challenges as they evolve. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner. Excellent opportunity for an Associate Project Coordinatorto join our Phase I Clinical Research business in Leeds, West Yorkshire on a full-time and permanent basis. This is a great opportunity to develop your career within Clinical research/trials and allow you to continue to practice your clinical skills and knowledge. You will be supporting Project Manager focusedon early phase studies.

Key Responsibilities

Your main responsibilities will include but not be restricted to:

  • Work with a more senior PC or PM in developing study specific documents ( e.g., Project Management Plan, Communication Plan, Investigator Package Plan, Risk Register, Project Specific Training Matrix and any other applicable plans as required), including compliance with client-specific requirements for low complex studies; distributes them to the study team and/or sponsor for review, compiles comments, and routes final documents.
  • Maintain an internal standardized filing structure for study-related documents; pro-activelymaintains documents within the filing structure.
  • Responsible for project setup activities ( e.g., study ID request, SAS Environment Setup request, eTMF, Study-specific Distribution Lists, etc.).
  • Attends and assists in the organization of study-related meetings, as required; distributes meeting agendas; maintains and distributes meeting minutes, Project Log, Risk Register, and study team contact lists; participates in client visits as needed.
  • As directed and with oversight, assists with business improvements initiatives to drive quality, productivity, and continuous improvements across different business units.
  • Upon PM request and with Associate Project Coordinator (PC) acceptance, may serve as a sponsor and site contact in the absence of the PM, primarily during maintenance phases of routine single and multi-site low-complexity trials.
  • Assists the PM or a more senior PC with payments per global finance standards.
  • Assists in the set-up, coordination and maintenance of sponsor/internal training in accordance with applicable SOPs and processes.
  • Assists in the development of project tools as required for the project ( e.g., screening and enrolment log and development of investigator training).
  • Assists the PM, or more senior PC as required with feasibility, including providing sites with feasibility questionnaire and tracking responses.
  • Assists the PM/more senior PC in maintaining overall project trackers, including financial, screening, and vendors.

Get ready to redefine what's possible and discover your extraordinary potential at Labcorp Drug Development . Here, 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.
Education/Qualifications:
  • University/college degree, preferably in a healthcare/scientific field. Specific clinical research experience may be substituted for education.
Experience:
  • Knowledge of the clinical trial process with early clinical pharmacology experience preferred.
  • Recent and relevant experience in a research environment.
  • Knowledge of protocol designs, study objectives, study procedures, and project-related timelines.
  • Knowledge of GCP/ICH Guidelines and applicable Regulatory Authority Guidelines.

Join us and discover why Labcorp Drug Development has been named by Forbes as one of the World's Best Employers 2020 and more than 90% of the top 20 global pharmaceutical companies are repeat customers. We can offer you not only a job, but a stable, long-term international career.

#LI-SP2

Company

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 —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert