Study Design Lead
Technical Project Management
We are recruiting for our Project Management team within our Central Laboratory Services 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.
We are currently offering several 12 months temporary contract and permanent contract, all full time position, based in our Geneva, Switzerland or Mechelen, Belgium office.
Within this position, your duties will include:
What we’re looking for
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.
Get to know Covance
Covance, the drug development business of LabCorp, is the world’s most comprehensive drug development services company. Because of our broad experience, from early research to commercialization, our more than 20,000 employees from across the globe are in a unique position to supply insights that go above and beyond testing. Our team’s impact on healthcare is remarkable. Through their everyday work they’ve supported 100% of the top 50 drugs on the market and all the oncology drugs approved in 2016. Even though we span multiple businesses, we operate as one, sharing our knowledge to improve our efficiency and deliver on the promise of a healthier world.
The Covance team is driven by an energized purpose to improve health and improve lives across the globe. Here, you’ll work alongside exceptional people who each play an important role in bringing new scientific discoveries and therapeutic area advancements to life. And, because we span the drug development spectrum, you’ll directly impact a wide-range of initiatives as you explore unique career paths and discover your extraordinary potential.
Get ready to make a difference as we speed the delivery of groundbreaking therapies and improve lives of countless individuals.
Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). 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