- Novo Nordisk (Lexington, MA)
- …working with stakeholders across multiple functions. The Associate Director , CQ, R&D Quality - will also act as the Clinical Quality Line of Business/ ... and serve as an Associate Directors for Clinical Compliance, Research & Development (R&D) Quality .... Compliance is one of four sister departments in Clinical Quality (CQ), which is part of… more
- University of Massachusetts Amherst (Amherst, MA)
- Associate Director of UHS Clinical Ops Apply now ... of the region. Job Summary The Associate Director of University Health Services (UHS) Clinical ...as mandated immunizations, health status and disability. + Leads quality assurance clinical programs, peer review and… 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 ... the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future,...merges biotech speed and agility with large pharmaceutical company quality , resources , and stability, uniting the best of… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Clinical Data Standards where you will be responsible ... the strategy for Takeda's global data standards, processes, and technologies across the clinical data continuum for quality of deliverables and global data… more
- Bristol Myers Squibb (Cambridge, MA)
- …writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing) + Site-facing ... + Activities related to data generation and validation, including CRF design, clinical data review/query resolution; ensure consistent, quality data review by… more
- Merck (Boston, MA)
- …to lead the coordination and execution of major change projects across Global Clinical Trial Operations. The role will also assist with Program Management Office ... initiatives and adapt plans based on evolving needs to ensure on-time, high- quality delivery in accordance with the stated project goals. + Ensure cross-initiative… more
- Kelly Services (Burlington, MA)
- **Sr. Manager/ Associate Director - Quality ...the Kelly Talent Community. Why Kelly (R) Science & Clinical ? Kelly Science & Clinical is your ... an experienced QA professional to support and evolve the quality management systems and processes at our US Site... function. This individual will report to the Sr. Director of Global GCP/GLP compliance and while working closely… more
- Frontier Medicines (Boston, MA)
- Join us as the Senior Manager/ Associate Director of Quality Assurance at Frontier, where precision meets purpose. In this pivotal role, you'll oversee ... knowledge sharing. + Familiarity with global regulatory and compliance requirements for clinical development and relevant quality standards, including but not… more
- Novo Nordisk (Watertown, MA)
- …and Cambridge reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct ... Boston R&D hub merges biotech speed and agility with large pharmaceutical company quality , resources, and stability, uniting the best of both worlds to develop new… more
- Boston Health Care for the Homeless Program (Boston, MA)
- …BONUS Boston Health Care for the Homeless Program (BHCHP) is seeking a talented Associate Medical Director of Medical Respite to work-in close collaboration with ... the Respite Medical Director and be responsible for the daily ...onboarding new hires, and conducting annual performance reviews. The Associate Medical Director will also work closely… more
- Bristol Myers Squibb (Devens, MA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director (AD) Quality Product Lead (eg, QPL, ... Quality Product Steward) for BMS is the responsible Quality representative for the lifecycle of commercial products/brands for the Biologics/Sterile Fill and… more
- Randstad US (Cambridge, MA)
- associate medical director . + cambridge ,...data on new treatments and practices to ensure high quality clinical service offerings. Advises non medical ... reports, safety related documents etc.) and assure production of high- quality documents + Supporting the Clinical lead...production of high- quality documents + Supporting the Clinical lead by: + Delivering medical oversight of the… more
- American Red Cross (Dedham, MA)
- …which includes the pre-analytic, analytic, and post-analytic phases of testing. + Ensure high- quality clinical lab test results required for patient care with ... and includes participation in multi-disciplinary research in collaboration with clinical teams, lead quality improvement initiatives, contribute to process… more
- Novo Nordisk (Lexington, MA)
- …best of both worlds to develop new medicines for patients. The Position The Associate Director in Medicinal Chemistry will be responsible for leading drug ... the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future,...goals. + Has accountability for CROs timelines and data quality + Has accountability and is a contributor to… more
- Sanofi Group (Framingham, MA)
- …Culture Development department within CCD located in Framingham, MA in the role of Associate Director . We are looking for a candidate with excellent scientific, ... Ensure highly scalable and robust commercial processes + Drive for product quality attribute understanding and control to meet comparability + Deliver thorough… more
- Bristol Myers Squibb (Devens, MA)
- …their personal lives. Read more: careers.bms.com/working-with-us . Position Summary: The Associate Director Supplier Relationship Manager (SRM) is accountable ... strategies. + Assures delivery of commercial supply that meets quality , compliance, schedule and budget expectations through proactive identification and… more
- Pfizer (Cambridge, MA)
- Position is Onsite/Hybrid **ROLE SUMMARY** + Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory ... rigorous statistical expertise on:Projects and protocols in support of clinical development and for publication, presentation, access negotiation, and other… more
- Sanofi Group (Cambridge, MA)
- …ensure the delivery of business objectives. + Enables the GRL by providing quality regulatory input and position to internal business partners, including but not ... limited to the clinical development teams, commercial and Global Regulatory Team for...Global Regulatory Team for assigned projects + Liaises with clinical , commercial, and other internal business partners in partnership… more
- Sanofi Group (Cambridge, MA)
- …ensure the delivery of business objectives. + Enables the GRL by providing quality regulatory input and position to internal business partners, including but not ... limited to the clinical development teams, commercial and Global Regulatory Team for...Global Regulatory Team for assigned projects + Liaises with clinical , commercial, and other internal business partners in partnership… more
- Novo Nordisk (Watertown, MA)
- …and Cambridge reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct ... Boston R&D hub merges biotech speed and agility with large pharmaceutical company quality , resources, and stability, uniting the best of both worlds to develop new… more