- Sanofi Group (Cambridge, MA)
- …for clinical trial initiation + Ensure that regulatory messaging for regulatory submission documents is aligned with program level and company objectives ... team** The team is involved in developing and executing regulatory strategies for Tzield in life cycle development stages...a later diagnosis. **Main responsibilities:** + Leads the US regulatory post-marketing activities. + As a key member of… more
- Sanofi Group (Cambridge, MA)
- …for clinical trial initiation + Ensure that regulatory messaging for regulatory submission documents is aligned with program level and company objectives ... **Main responsibilities:** + Leads the US regulatory activities. + As a key member of the Global Regulatory Team (GRT), and strategic partner to the Global … more
- Sumitomo Pharma (Boston, MA)
- ** Associate Director , GMP Quality Control** Sumitomo Pharma America (SMPA) is focused on delivering therapeutic and scientific breakthroughs in areas of critical ... seeking a dynamic, highly motivated, and experienced individual for the position of Associate Director of GMP Quality Control, who oversees GMP compliance of… more
- AbbVie (Worcester, MA)
- …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Quality Control provides leadership and direction to the ... Quality Function they are responsible for within Operations. This Associate Director , Quality Control is responsible for...authority on job specific aspects of the Quality and Regulatory compliance program for the site. +… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will be responsible for the ... strategic and tactical labeling expertise to teams while ensuring compliance with applicable regulatory requirements. You will serve as the regulatory expert for… more
- Bristol Myers Squibb (Cambridge, MA)
- …future therapeutics. Reporting to Senior Scientific Director Translational Medicine, the TM Associate Director will be part of the late stage TM group. The ... for the pipeline and supports the late-stage portfolio for regulatory , translational development and life cycle management. The Immunology, Cardiovascular,… more
- Curia (Burlington, MA)
- Associate Director , Human Resources - Burlington, MA Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology ... industries. The Associate Director , Human Resources is responsible for...development, performance management and any other employee-orientated practice or program that will attract, motivate and retain the workforce.… more
- Wolters Kluwer (Boston, MA)
- …the technology transformation efforts to highlight the maturity of WK's cybersecurity program . + Collaborate with peers across GBS teams to align compliance ... and reported to demonstrates the effectiveness of the security compliance program . Compliance Oversight and Responsibilities: + Educate control owners and business… more
- Regeneron Pharmaceuticals (Boston, MA)
- The Associate Director , Clinical Imaging will own the strategy and execution of sophisticated early and late phase oncology imaging in clinical trials where ... clinical studies. We assume you will be a member of cross-functional program teams including Regeneron clinical and preclinical colleagues as well as external… more
- Bristol Myers Squibb (Cambridge, MA)
- …pharmaceutical industry for the Sr. Research Investigator level or 5+ years for the Associate Director level. No additional industry experience is needed for the ... $121,000 - $167,2000, plus incentive cash and stock opportunities (based on eligibility). ** Associate Director :** the starting compensation for this job is a… more
- Wolters Kluwer (Boston, MA)
- …Corp in the **New York Office.** The position is remote. The Associate Director (Sr. Engineering Leader) of the Salesforce Program will manage the enterprise ... **Wolters Kluwer CT Corporation (CT)** is looking for an ** Associate Director ** **, Salesforce** to join CT… more
- Pfizer (Cambridge, MA)
- …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
- Sanofi Group (Cambridge, MA)
- …gastrointestinal diseases. **Main Responsibilities:** The Global Medical Immunology Pipeline Associate Director , Gastroenterology, reports to the Global Medical ... care. We curate patient and scientific evidence and partner with commercial, regulatory , R&D, market access, and external affairs teams to develop therapeutic… more
- Takeda Pharmaceuticals (Lexington, MA)
- …true to the best of my knowledge. **Job Description** **Job Title** : Associate Director , Upstream Manufacturing Operations **Location** : Lexington, MA **About ... + Participate in facility and process inspections by domestic and international regulatory agencies. Ensure that all SOPs and batch records are maintained to… more
- Bristol Myers Squibb (Boston, MA)
- …data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing ... leadership. + Ensures appropriate regional management of speaker lists and speaker program support (if applicable) + Contributes FM expertise to regional accounts… more
- Frontier Medicines (Boston, MA)
- Join Frontier Medicines on an exciting journey as our newest Senior Manager/ Associate Director in CMC Development, located at either our Boston or South San ... drug substance process development and manufacturing + Coordinating drug substance program management + Engaging with CROs/CDMOs and identifying new technologies +… more
- Randstad US (Cambridge, MA)
- associate medical director . + cambridge , massachusetts (remote) + posted april 2, 2024 **job details** summary + $90 - $117.69 per hour + contract + ... trial process based on previous experience + Good knowledge of regulatory requirements/ICH guidelines + Good organizational and communication skills, able to… more
- Novo Nordisk (Lexington, MA)
- …to develop new medicines for patients. The Position We are looking to hire an Associate Director of Clinical Operations. This is a unique opportunity to work in ... with study protocol, and identifying areas of concern and escalating to Clinical Program Lead when appropriate + Collaborate with the Clinical Trial Lead and study… more
- Sanofi Group (Cambridge, MA)
- …Our Medical function serves as a key strategic partner with commercial, regulatory , clinical, and market access on therapeutic solutions to support patients' needs. ... respiratory, and gastrointestinal diseases. **Main responsibilities:** The Global Medical Director of the Dermatology, reports to the Global Medical Head… more
- Bristol Myers Squibb (Cambridge, MA)
- …and validation of clinical study reports (CSRs) and clinical portions of Regulatory Documents (eg, IB, DSUR, regulatory responses) + Collaborate and ... statistics, clinical operations + Proficient knowledge and skills to support program specific data review, trend identification, data interpretation + Knowledge of… more