We're looking for a Clinical Regulatory Affairs Associate III, working in the Pharmaceuticals & Medical Products industry in Lake Bluff, Illinois, United States.
Plans and negotiates publishing timelines with the teams.
Manages multiple projects and competing priorities.
Plans and conducts submission team meetings.
Communicates effectively verbally and in writing with diverse audiences and across various levels within the organization.
The pay range we're offering is 40 to 42 per hour. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
4 years pharmaceutical or industry related experience
Experience in Regulatory Affairs preferred but may consider QA, R&D/support, scientific affairs, operations or related area
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.