- Parexel (Hartford, CT)
- …and approved programs, helping to shape the future of life-saving therapies. As a **CMC Regulatory Affairs Senior Associate ** , you will play a ... (advanced degree preferred). + 4+ years of experience in CMC Regulatory Affairs within the pharmaceutical or biotechnology industry. + Proven experience… more
- Sumitomo Pharma (Hartford, CT)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director, Regulatory Affairs (Oncology).** The Associate ... Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She will...Comfortable presenting to all levels of the organization including Senior Management. **Education and Experience** + Bachelor's degree in… more
- United Therapeutics (Hartford, CT)
- …or pharma regulatory experience with a Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic ... experience with a Master's Degree in life sciences, quality, regulatory affairs or a related area of...Ability to mentor, coach, guide, and train lower to senior level employees **Preferred Qualifications** + Proficient knowledge of… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Associate Director, Medical Affairs Strategy Team Member serves ... organized customer channels including Health Systems and Payers. The Senior Associate Director, Medical Affairs ...industry. + One-plus (1+) years of experience in Medical Affairs , Clinical Trials, Regulatory , or related area… more
- Boehringer Ingelheim (Ridgefield, CT)
- …field with eight to ten (8-10) years' experience in the pharmaceutical industry in Regulatory Affairs or scientific discipline required OR Master's degree with a ... or related field with six (6) years' experience in the pharmaceutical industry in Regulatory Affairs or scientific discipline required. + Minimum five (5) years… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Senior Clinical Program Leader assumes global Clinical Development responsibilities supporting early or late development projects, reporting to ... the Associate Global Head or the Global Clinical Programme Team Leader. The Senior Clinical Program Leader has a medical leadership role for a project or a… more
- Otsuka America Pharmaceutical Inc. (Hartford, CT)
- …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to ... ** Associate Director, Small Molecule Analytical Development** + Lead...and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and facilitation skills. + Strong track record of interactions with regulatory affairs authority, international societies and other relevant stakeholders. ... **Description** This role will serve as the Associate Head of Experimental Medicine for a given...years (combination of hospital, academic and industry experience),inclusive of senior leadership role/s; Clinical / pharma experience in the… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and facilitation skills. * Strong track record of interactions with regulatory affairs authority, international societies and other relevant stakeholders. ... **Description** This role will serve as the Associate Head of Experimental Medicine for Inflammation/ Immunology Rheumatology and Gastroenterology and has overall… more