Covance BioA Study Coordinator II
Play a pivotal role in the drug development process and grow your career
Are you interested in making a real scientific impact through your everyday work? Would you enjoy working in a team-focused environment as you explore unique career opportunities?
If you are looking for a company where you can gain exposure to a wide variety of science and explore a path forward into project management, consider working at Covance as a BioA Study Coordinator in their Madison, WI facility.
In this role you will clients and internal project manager and lead scientists to draft study documentation in accordance with proposal outline or client-supplied information. Documents include: draft protocols, sample analysis outline, and study schedules. You are also responsible for ensuring that the study is in compliance with SOP, protocol, and regulatory agency guidelines. You will also be expected to:
What we’re looking for...
BioA Study Coordinators are the most successful at Covance with:
Thrive personally and professionally at Covance
Working at Covance, you’ll continue to grow in our learning-based culture so you’ll know how to expertly respond and adapt as the industry continues to evolve. Here, you’ll put your education to work as you play a meaningful role in advancing healthcare.
We offer a comprehensive benefits package. This includes 21 days of personal time off, 7 paid holidays, medical and dental insurance as well as tuition reimbursement, a 401(k) plan with a generous company match, along with short and long-term disability and life insurance.
Why Study Coordinators choose to work at Covance