Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

Study Design Lead in Geneva or Mechelen

Company: Covance
Location: Mechelen
Reference: 14854
Closing Date: 07 Dec 17
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.  We are recruiting for our Project Management team and are currently seeking to hire a Study Design Lead to help support the team. This is a full time position, based in our Geneva, Switzerland or Mechelen, Belgium office.

Requirements:

About the job:

Within this position, your duties will include:

  • Interacts with the clients (pharmaceutical companies) to define study design choices and works with Covance internal stakeholders to highlight risks and budget impacts associated with study design
  • Takes the lead to accurately interpret clinical protocol requirements and coordinate the preparation of Covance clinical trial databases.
  • Leverages technical, therapeutic area and pharmaceutical industry knowledge to successfully coordinate the completion of Covance clinical trial database.
  • Liaises with internal departments to understand Covance capabilities and assesses feasibility of requests in order to meet client needs related to study design
  • Coordinates internal processes and communications related to study design (including but not limited to: internal feasibility requests, material transfer agreements and supply forecasting) and ensures the eventual follow up is documented and global monitoring plan implemented. Performs quality self-review
  • Displays strong interpersonal and communication skills that will build strong internal and external relationships to ensure high quality study design
  • Ensures that all customer requirements with relation to study design are documented and acted upon
  • Able to act efficiently in an environment with dynamic timelines and priorities
  • Displays appropriate self-organization and ability to manage conflicting priorities
  • Participates in functional meetings and provides input, keeping processes up to date
  • Complies with CCLS Global Project Management strategy
  • Supports a culture of continuous improvement, quality and productivity
  • Other duties as assigned

 

About You:

To be successful in this position, you will need to be educated to High school diploma level (or equivalent) and/or University degree in a scientific field in a relevant area.

Additionally, you will need to demonstrate 3 years of previous industry experience in managing Clinical Trial projects or in designing clinical databases.

 

We Offer:

Covance offers a comprehensive benefits package including health cover and a contributory pension.

 

Get ready to redefine what’s possible and discover yourextraordinary potential at Covance. 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 anenergized 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.

 

There is no better time to join us!

Apply for this job: Study Design Lead in Geneva or Mechelen

Contact Information:

Address:  Covance -Geneva
7 Rue Moïse-Marcinhès, 1217 Geneva, Meyrin, Switzerland
1217
Switzerland
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.