- Takeda Pharmaceuticals (Providence, RI)
- …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
- Takeda Pharmaceuticals (Providence, RI)
- …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
- Takeda Pharmaceuticals (Providence, RI)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned products… more
- Merck (Boston, MA)
- …with worldwide regulatory agencies and/or subsidiaries with regard to global regulatory strategy/registration requirements for one or more our company's ... submissions and associated documentation. + Provides expertise as the Global Regulatory Lead to Product Development Teams...but are not limited to:** + Reports to Executive Director or Associate Vice President, Therapeutic Area… more
- S&P Global (Boston, MA)
- …Level (for internal use):** 11 **The Team:** S&P's Network and Regulatory Compliance group offers best-in-class technology and incorporate industry best practices ... financial services industry with meeting their compliance obligations. Our risk and regulatory compliance management solutions create a single source of truth for… more
- Rhythm Pharmaceuticals (Boston, MA)
- …tenacity to overcome barriers, together. Opportunity Overview Rhythm is looking for an Associate Director QA to play a leadership role in strengthening Rhythm's ... system that houses all of Rhythm's GxP records. The Associate Director QA will lead the Quality...global network of researchers, a track record of regulatory successes and global commercial infrastructure to… more
- Merck (Providence, RI)
- …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
- Merck (Providence, RI)
- …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
- Takeda Pharmaceuticals (Boston, MA)
- …will inspire you and empower you to shine? Join us as an Associate Director Translational Biomarker Lead Inflammation/Autoimmune disease, ECD in our Cambridge, ... people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for… more
- Merck (Providence, RI)
- …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
- Takeda Pharmaceuticals (Boston, MA)
- …excellence and portfolio progression for the Takeda Research pipeline. The Associate Director , Strategic Outsourcing will provide strategic oversight and ... people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for… more
- Takeda Pharmaceuticals (Boston, MA)
- …bring life-changing therapies to patients worldwide. Join Takeda as a Research Scientific Associate Director : TME Tumor Discovery Lead, ODDU where you will drive ... in-licensing or partnering. + Help prepare, edit, and review documents for regulatory submission including study reports, IB's, IND's. + Frequent contact and… more
- Zimmer Biomet (Plainville, MA)
- …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
- Ford Motor Company (Providence, RI)
- …ready to change the way the world moves? **In this position ** As the Associate Director of M&A Integration, you will lead the strategic integration of merged ... smooth transition. + Ensure that all integration activities comply with regulatory requirements and company policies. + Drive synergy identification and realization,… more
- Takeda Pharmaceuticals (Boston, MA)
- …to bring life-changing therapies to patients worldwide. Join Takeda as a Research Scientific Associate Director : TME Tumor Lab, ODDU where you will contribute to ... Preference for those with experience preparing/editing/reviewing of documents for regulatory submission (ie, study reports, IB's, IND's). **Minimum Requirements/Qualifications:**… 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 ... of Medical Strategies, Objectives and FM Plans within boundaries established by regulatory and legal compliance in accordance with company policies and sound ethical… more
- Takeda Pharmaceuticals (Boston, MA)
- …people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for ... everything we do. We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver **_Better Health and… more
- IQVIA (Boston, MA)
- …In depth knowledge of, and skill in applying applicable clinical research regulatory requirements; ie, Good Clinical Practice (GCP) and International Conference on ... travel _This is a remote / WFH opportunity_ IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the… more
- Merck (Boston, MA)
- … regulatory filing, and publication. **Specifically, The Senior Clinical Director May Be Responsible For:** + Evaluating pre-clinical and translational work ... **Job Description** The **Senior Clinical Director (Sr. Principal Scientist)** has primary responsibility for the strategic planning and directing clinical research… more
- CSL Plasma (East Providence, RI)
- …as or delegates to another appropriate physician the duties of "laboratory director ", "technical consultant", or "clinical consultant" as prescribed by the Clinical ... although such training may be delegated to an approved Medical Staff Associate . Trains other physicians. Evaluates newly trained Medical Staff Associates for… more