- Catalent Pharma Solutions (Bloomington, IN)
- **We're hiring for a Senior Regulatory Affairs Specialist to support compliance and regulatory affairs in Bloomington, Indiana!** Catalent is a ... are essential to our mission: to help people live better, healthier lives. The ** Senior Regulatory Affairs Specialist ** serves as the liaison to clients… more
- Zimmer Biomet (Warsaw, IN)
- …for impact on regulatory status of the product. + Follow Zimmer Biomet regulatory affairs policy and procedures. + May provide training and/or guidance to ... and governmental agencies. **Your Background** Requires a Bachelor's degree in Regulatory Affairs , Engineering, or Life Sciences, or related field. Requires… more
- Veterans Affairs, Veterans Health Administration (IN)
- Summary The Program Specialist is responsible for managing and supporting national VHA programs and activities that fall under the purview of ILEAD's, Employee and ... appropriate offices throughout the country and receive the necessary concurrence from senior VHA leadership and program oversight committees. Outline and maintain a… more
- Merck (Indianapolis, IN)
- **Job Description** The Senior Professional Services Veterinarian- Dermatology Specialist will function to support the commercial, medical, and business needs of ... may include, but are not limited to: + Utilizes specialist knowledge and experience in dermatology to serve as...leaders of diverse expertise and backgrounds, and assist medical affairs in developing and guiding advisory boards + Represent… more
- Immigration and Customs Enforcement (IN)
- …Assistant Director for Healthcare Compliance, Office of Health Plan Management. The Senior Utilization Review Consultant will report directly to the IHSC Regional ... position Responsibilities DUTIES AND RESPONSIBILITIES: Serves in the capacity of Senior Utilization Review Consultant and subject matter expert in program activities… more
- Lilly (Indianapolis, IN)
- …areas relevant to drug discovery or development, eg epidemiology, toxicology, pharmacovigilance, regulatory affairs + Experience within Global Patient Safety or ... detection and clarification, preparation of device safety reviews, support for regulatory inquiries, input into device development and risk management activities,… more