- Takeda Pharmaceuticals (Hartford, CT)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Project Management and Strategic ... Regulatory Affairs Team. **How you will contribute:** + As Associate Director , Global Regulatory Project Management and Strategic Planning, you… more
- Boehringer Ingelheim (Ridgefield, CT)
- …Persons with a non-science degree having relevant professional experience may be considered. + Associate Director level: must have three to five (3-5) years of ... product labeling. Participate in Human Pharmaceutical Review Committee, providing regulatory opinion on promotional communications. Review scientific exchange communications… more
- 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)
- …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
- Merck (Hartford, CT)
- …component of decision-making at our 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)
- **Description** The Associate Director of Drug Substance - EACD will have the primary responsibility to oversight process development and manufacturing ... manufacturing activities of clinical/commercial stage small molecule APIs. Reporting to the Director of EACD, this individual will provide guidance to the external… more
- Merck (Hartford, CT)
- …Pharmacometrics -** **Immune/Oncology** **(QP2-IO)** team in the role of Associate Director QP2-IO team is part of the Global Clinical Development ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… 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 Oncology 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)
- …Medical Device and Combination Product (MDCP) Quality Assurance Operations team, the Associate Director Quality Engineering & Quality Assurance is responsible ... reviewing and approving medical device/combination product documentation to support regulatory filings and audits of data, policies, procedures, and systems… more
- Boehringer Ingelheim (Ridgefield, CT)
- …benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Associate Director , Content Enablement is responsible to translate the asset ... and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering… more
- Boehringer Ingelheim (Ridgefield, CT)
- …programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Associate Director , Access & Affordability programs will lead the overarching ... of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate...to: Value & Access, TA Marketing and Sales, Legal, Regulatory , Compliance, HP Operations. + Leads and develops direct… 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
- Boehringer Ingelheim (Ridgefield, CT)
- …programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Associate Director , Medicine Capability Process Excellence Owner defines the US ... and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering… more
- Bristol Myers Squibb (Stamford, CT)
- …data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing ... of Medical Strategies, Objectives and FM Plans within boundaries established by regulatory and legal compliance in accordance with company policies and sound ethical… more
- Zimmer Biomet (Hartford, 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
- 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
- Boehringer Ingelheim (Ridgefield, CT)
- …develop and motivate HEOR Value Demonstration and Translation Team staff at the Director , Associate Director and Manager levels. Collaborate with HEOR ... alignment with the US Market Access Department, the Executive Director ensures that the HEOR Value Demonstration Team (VDT)...of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate… more