Covance

Study Design Lead

CH-Geneva | BE-Mechelen
Job Number
2017-16063
Job Category
Other
Position Type
Full-Time

Job Overview

Study Design Lead

Technical Project Management

 

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. As a Study Design Lead you should be knowledgeable and experienced in study design techniques related to the creation and maintenance of the Covance Statement of Work document (key client deliverable) and should demonstrate leadership across the Covance study team, keeping a collaborative attitude and fostering excellent communication within the team, demonstrate agility to deal with conflicting priorities and possess appropriate self-management skills.

 

This is a permanent contract, full time position, based in our Geneva, Switzerland or Mechelen, Belgium office.

 

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 partners 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.
  • Demonstrates 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 handle conflicting priorities
  • Participates in functional meetings and provides input, keeping processes up to date
  • Follows 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 running Clinical Trial projects or in designing clinical databases.

 

We Offer

The opportunity to work within an experienced and highly skilled team.

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

Get ready to redefine what’s possible and discover your extraordinary 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 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 ground breaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.

 

Education / Qualifications

Minimum Required:

  • High School Diploma

Preferred:

  • University degree in a scientific field

Experience

Minimum Required:

3 years of previous experience as a CCLS Regional Study Coordinator or 2 years of previous experience as Global Study Manager (I or II), Clinical Database Designer or other equivalent industry experience in designing clinical databases

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