Study Design Lead
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 12 months contract (renewable), full time position, based in our Geneva, Switzerland or Mechelen, Belgium office.
Within this position, your duties will include:
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.
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.
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