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Job Details

Clinical Project Coordinator II (Early Clinical Development), Leeds

Company: Covance
Location: Leeds
Reference: 64206BR
Closing Date: 21 Dec 16
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

We are recruiting for our Early phase Clinical Operations team in Leeds and are currently seeking to hire a Project Coordinator. This is a full time, permanent position based in our Leeds office.

Requirements:

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. 
We are recruiting for our Early phase Clinical Operations team in Leeds and are currently seeking to hire a Project Coordinator. The Project Coordinator will support the team by assuming Primary responsibility for the coordination and completion of all administrative functions in support of the project manager responsible for overall management of multi-site clinical studies. This is a full time, permanent position based in our Leeds office. 

About the Job:
Within this role, you will be expected to consistently comply with GCP standards, as well as driving efficiency and quality in coordination activities and applicability to clinical trial management and learning and applying drug development process knowledge. 

Additionally, your responsibilities will include: 

  • Providing administrative support for effective Clinical Trial Core Team Operations 
  • Coordinating meetings, study specific training, optimising tracking, and filing processes 
  • Administering Study Plans 
  • eTMF document upload 
  • Original document management 
  • Coordinating eTMF quality reviews 
  • CTMS/eTMF set up per BP&S standards 
  • Developing Protocol Tools 
  • Developing Inv Training 
  • Creating and maintaining Regulatory Binders 
  • Granting EDC access, and access to other study required systems 
  • CTMS Updating and Data Monitoring 
  • Leading eTMF Audit Readiness 
  • Ensuring Payments per Global Finance standards 
  • Creating ADI Logs and/or taking minutes 
  • Creating and maintaining trackers 
  • CTMS/eTMF set up per BP&S standards 
  • Coordinating Study/Sponsor Specific Training 
  • Conducting feasibility activities 
  • Performing other duties as assigned by management to support study teams needing collaborative support 


About You:
To be successful in this position, you will need to demonstrate: 

  • 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 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 
  • Some demonstrable experience of working within a clinical trials operations environment, including an understanding of the drug development life cycle 



We Offer:
COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. 
Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. 
At Covance, we help make the miracles of medicine a reality. 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 miracle of medicine to market sooner. 

There is no better time to join us!

Apply for this job: Clinical Project Coordinator II (Early Clinical Development), Leeds

Contact Information:

Address:  Covance Leeds
Leeds

England

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