Job Overview : Study Design Lead
Study Design Lead
Technical Project Management
Are you ready for an intellectual challenge that demands refined communication skills? If you have a Life Sciences degree and want to reach your extraordinary potential helping us make ground-
breaking deliveries through clinical studies, then joining our study team as a Study Design Lead (SDL) in our Mechelen or Brussels office could be the next step in your career.
This role is also eligible for remote work in Belgium.
Our SDLs thrive in an ever-changing environment. Moving quickly amongst technical conversations with internal and external players, their ability to truly understand a problem and guide a solution makes them successful both with our pharmaceutical clients and in our mission to improve health and improve lives.
Housed in Covance Central Laboratory Services (CLS), this is a permanent contract role that is crucial to our growing facilities in Mechelen.
About the Job
You’ll join our Global Project Management Department, a team of exceptional people who are unified by an energizing purpose to transform healthcare and improve lives around the globe.
Clinical studies are developed and managed collaboratively by a study team, in which the SDL plays an essential role by designing the Covance Statement of Work (SOW).
This critical document, which translates the study protocol provided by our clients, guides all services provided by Covance CLS throughout the course of a clinical trial.
SDLs have multiple studies in their portfolio and responsibilities for each include :
You must have a university degree in Life Sciences. We value candidates who are on a path of continuous learning; a PhD is an asset but not required.
You must demonstrate related industry experience, either through education or employment. Previous experience running clinical trial projects or designing clinical databases is preferred.
opportunities for advancement; and a community of hard-working people who push new boundaries together.
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.
Please apply by submitting a CV in English.
This position is only available for candidates elligible to work in Belgium
Education / Qualifications :
Expience in clinical trials is preferred