Are you interested in making an impact through your everyday work? Are you passionate about advancing your career while making a difference in patients’ lives? Do you love to organize projects and thrive in a dynamic, high-paced environment?
If you said yes to these questions and you are looking for a place where you can explore a multitude of career paths across the drug development spectrum, consider working at Covance as a Study Design Lead. This is a permanent, full time position, based in our Indianapolis office or it can be remotely based.
As a Study Design Lead, you will collaborate with our pharmaceutical company clients to review clinical protocols, define the components of clinical trial study designs, and work with internal teams to highlight risks and financial impacts associated with various study design options. In this position, you will be responsible for the following:
Accurately interpreting clinical protocol requirements and coordinating the preparation of Covance clinical trial databases
Utilizing technical, therapeutic area, and pharmaceutical industry knowledge to successfully coordinate the completion of Covance clinical trial databases
Coordinating internal processes and communications related to study design and ensuring that follow-up actions are recorded and global monitoring plans are implemented
Ensuring that all customer requirements are documented and acted upon
Building strong relationships to ensure high quality study design
Do you have the following education and experience?
Bachelor of Science degree (flexible to consider those without a degree that have significant related experience)
Minimum of 3 years of study design experience (can include clinical database design)
Minimum of 2 years of experience interpreting and translating clinical protocols
Technical writing experience is desirable
Experience managing Clinical Trial Projects or designing clinical databases is a plus
Education/Qualifications:
Bachelor of Science degree preferred(flexible to consider those without a degree that have significant related experience)
High School diploma required
Experience:
Minimum of 3 years of study design experience (can include clinical database design)
Minimum of 2 years of experience interpreting and translating clinical protocols
Technical writing experience is desirable
Experience managing Clinical Trial Projects or designing clinical databases is a plus
Salary.com Estimation for Study Design Lead in Indianapolis, IN
$70,287 to $95,261
If your compensation planning software is too rigid to deploy winning incentive strategies, it’s time to find an adaptable solution.
Compensation Planning
View Core, Job Family, and Industry Job Skills and Competency Data for more than 15,000 Job Titles
Skills Library
Sign up to receive alerts about other jobs with skills like those required for the Study Design Lead.
Click the checkbox next to the jobs that you are interested in.