- Takeda Pharmaceuticals (Hartford, CT)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will be responsible ... You will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements are met for… more
- Boehringer Ingelheim (Ridgefield, CT)
- …labeling. Participate in Human Pharmaceutical Review Committee, providing regulatory opinion on promotional communications. Review scientific exchange communications ... of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate...monitor reliable sources from which to obtain product and/or regulatory information. + Review and signature of FDA forms… more
- Boehringer Ingelheim (Ridgefield, CT)
- …you with the opportunity for significant professional development. The (Senior Associate ) Director is a key member of global , cross functional product teams ... This may include high profile committees such as FDA advisory committees, global regulatory authority meetings, Advisory Boards, Board of Managing Directors,… more
- Sumitomo Pharma (Hartford, CT)
- ** Associate Director , GMP Quality Control** Sumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of critical ... highly motivated, and experienced individual for the position of Associate Director of GMP Quality Control, who... ensures compliance with GMPs, SMPA procedures and applicable global Regulatory guidelines by providing oversight and… more
- Merck (Hartford, CT)
- …component of decision-making at ouor company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and… more
- Boehringer Ingelheim (Ridgefield, CT)
- …are delivered in compliance with GCP requirements and global regulatory and ethical standards. **Requirements** **Requirements for Director Level:** + ... programs with the objective to accelerate clinical development and achieve regulatory approvals and reimbursable medicines. Senior CPL provides continuous medical… more
- Boehringer Ingelheim (Ridgefield, CT)
- …methods consultation to cross- functional and cross-regional colleagues. **Requirements** **Sr. Associate Director :** + Doctoral or Master's degree in ... analytical background. + Overview-level knowledge of one or more global healthcare systems. ** Director :** + Doctoral or...appropriate level based upon education and experience._ The Sr. Associate Director position offers a base salary… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** ** Associate Director Requirements:** + US MD or DO degree or ... our motivated and expert team of physicians in the global Inflammation Therapeutic Area of Patient Safety and Pharmacovigilance...more than 2 years of applicable experience, required. **Sr. Associate Director Requirements:** + US MD or… more
- Wolters Kluwer (Hartford, CT)
- …here. (https://youtu.be/OZ2kSzAaXK4?si=sDgZ7DZUbMnBddMq)** **What We Offer: ** The Market Research Associate Director role offers growth potential opportunities, ... Wolters Kluwer is a global leader in professional information services that combines...benefits. **What You'll be Doing:** As our Market Research Associate Director , you will share your in-depth… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Associate Director , Medical Coding, Analytics & Process is responsible for ... and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering… more
- Merck (Hartford, CT)
- …on time, every time, across the globe. **Position Responsibilities:** + The Associate Director is responsible for performing comprehensive and detailed GMP ... with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract… more
- Merck (Hartford, CT)
- …(QCI) colleagues, GCTO Country Operations, other GCTO functional areas, Pharmacovigilance (PV), Global Regulatory Affairs and Clinical Safety (GRACS), IT, etc.) ... the global inspection tracking system that tracks all GCP Regulatory Health Authority inspections, findings, responses and Corrective Action and Preventive… more
- Boehringer Ingelheim (Ridgefield, CT)
- …**_Candidate will be hired_** **_at level commensurate with experience and education._** **Sr. Associate Director Requirements:** + US MD or DO degree or ... Physician will join our motivated and expert team of physicians in the global CREA Therapeutic Area of Patient Safety and Pharmacovigilance at BI, whose priority… more
- Boehringer Ingelheim (Ridgefield, CT)
- …employees. Within the Go-To-Market ("GTM") Services Media Center of Excellence, the Associate Director , Consumer & Professional Media, will use deep knowledge ... of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate...the DTC Media agency delivery. Collaborates close with the Director on executing key priorities for the Media CoE.… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Associate Director , External Research, Scientific Affairs provides strong subject matter expertise, operational oversight and process ... and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering… more
- Pfizer (Groton, CT)
- …clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices. + Provide scientifically ... access negotiation, and other evidence generation efforts for Pfizer products; Regulatory and Health Technology Assessment (HTA) submissions; and projects to… more
- Zimmer Biomet (Stamford, CT)
- …included, respected, empowered, and recognized. **What You Can Expect** The Program Associate Director will oversee lifecycle management business processes to ... of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a...- Research, Business Development, Finance, Clinical, Commercial, Legal and Regulatory . + Analyze the data related to the portfolio… more
- Bristol Myers Squibb (Stamford, CT)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Summary** The Regional Associate Director (RAD) role is field-based and focused on ... of Medical Strategies, Objectives and FM Plans within boundaries established by regulatory and legal compliance in accordance with company policies and sound ethical… more
- Sanofi Group (Hartford, CT)
- …Medical function serves as a valued strategic partner with Clinical, Commercial, Regulatory , and Market Access on therapeutic solutions to support patients' needs. ... patients. **Job Description:** This position reports to the Senior Medical Director , Respiratory/Allergy. Main job responsibilities: + In partnership with the… more
- Pfizer (Groton, CT)
- …You will be part of a team of nonclinical statisticians within Pfizer's Global Biometrics and Data Management organization. There is no management of people in ... for the design, analysis, reporting, and interpretation of exploratory, regulatory , and investigative nonclinical safety studies. + Provide critical experimental… more