Project Coordinator II
- Employer
- Labcorp
- Location
- Warsaw, Poland
- Salary
- Competitive
- Start date
- 29 Sep 2020
- Closing date
- 26 Oct 2020
View more
- Discipline
- Clinical Research
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Covance, the drug development business of LabCorp® has supported the pharmaceutical industry develop more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today.
In 2019,weestablished our Project Management Academy. This is our center of excellence to identify early talent and develop them into future Covance project managers.
As partof our ongoing growth weare looking for Project Coordinators to join our Warsaw Project Management Academy.
Main responsibilities:
- Acts as a SME on study specific processe
- Project expertise for CTMS reporting, study metrics, risk management regarding communication, coordination, and eTMF quality
- Able to co-ordinate and manage support across large global study
- Applies therapeutic knowledge to daily activities of the clinical trial, brings new knowledge to the team, drives best practices in coordination, communication and documentation
- Provides administrative support for effective Clinical Trial Core Team Operations
- Provides support with project planning & forecasting (inc plans & Project Schedule, TAQs)
- Provides support with reviewing and managing all aspects of project (financials, enrollment, vendors, etc).
- Attend and coordinate study meetings internal, sponsor, (including KOM, IM, as needed, working with Scarrit as needed).
- Develop Protocol Tools, Coordinate study plans and development and support management of study plans, guidelines, utilized MS Project for timelines with the ICRA
- Develop Inv Training
- Regulatory/Pharmacy Binders and study materials.
- Create and revise Project Specific Forms
- CTMS updating
- Payments for manually tracked (AsiaPac)
- ADI logs and Agenda/minutes/Slide decks
- Manage and maintain Sponsor system portals
- Provides Site and team communications
- Drafts and formats Newsletters
- Assist with coordinating Audits (assist in response to internal audits and CAPA resolutions)
- Follow up on Governace portal issues
- Trackers (including financial and vendors)
- Vendor Mgt if no Vendor Manager
- Performs other duties as assigned by management to support study teams and needing collaborative support
University/college degree, or certification in a related allied health profession (i.e. nursing, medical or laboratory technology), in lieu of college degree candidate may have 5 years relevant industry experience.
- Knowledge of the clinical trial process with early clinical pharmacology experience preferred
- Computer competency with various programs (e.g., Microsoft Word, Excel, Project, Access and Power Point)
- Ability to develop accurate study related documents with minimal supervision
- Ability to communicate verbally and in writing
- 2 years of relevant industry experience
- Additional experience may be submitted for education requirements
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.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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