Covance Document Coordinator II
Play a pivotal role in the drug development process and grow your career
Are you interested in making a real 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 scientific breakthroughs and explore a multitude of career paths across the drug development spectrum, consider working at Covance as a Document Coordinator II in our Greenfield, IN facility.
In this role you will support out BioCMC laboratories by managing the process for issuing protocols, amendments and reports. You will also be reponsible for SOPs, study and non-study related documentation and the controlled forms system overall.
Excellent word processing, excellent written English, some knowledge of GMP regulations, ability to learn new software, flexible, team player. Able to sit for long periods of time. Team player.
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 choose to work at Covance
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. 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.