Covance is expanding and is looking to recruit a Senior Regulatory Submissions Associate (Lead) to join the team, the successful candidate can be based anywhere in the UK/EU. The role is responsible for the timely preparation of submissions to Regulatory Authorities in support of investigational and marketed products. You will Interact with Regulatory Authorities and with clients to support regulatory activities. Proactively interact with other Covance groups and clients to provide guidance regarding Regulatory Authority requirements and project timelines and requirements. Working with minimal supervision, it is the responsibility of the Senior Regulatory Associate to have oversight and coordination of the submission activities across the EU/Globally and to also prepare documents to the required standard and to maintain awareness of current regulatory standards related to submissions for drug and biologic products. This position may also have supervisory responsibilities.
A career at Covance provides our employees the unique chance to create an immediate impact and difference in our patient’s lives. Joining Covance will offer a rewarding career, a chance to work in a high-energy & team oriented work place, and access to competitive benefits. With the support of exceptional people from across the globe and a vast array of career options, you’ll be empowered to own your career journey with mentoring, training and personalized development planning. As a Covance employee, your work will be meaningful, the patient outcomes are real, and the results are lasting.
Our mission is to help our clients bring the miracles of medicine to market sooner -- join us for your next career move.
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.
Recommended: Bachelor’s Degree in Life Sciences or equivalent.