- Merck & Co. (North Wales, PA)
- …the ability to:--Strong knowledge of clinical research regulatory requirements (eg, GCP and ICH) Proven ability to manage competing priorities and effectively ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents… more
- Merck & Co. (Rahway, NJ)
- …- Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. - Preferred Experience and Skills: - - Proficiency ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents… more
- Clinical Dynamix, Inc. (Waltham, MA)
- …to the Sr. Director , Clinical Excellence Operations the Senior Manager/ Associate Director , Records Management will be responsible for expertise, oversight, ... across all therapeutic areas of development at Company. The Associate Director of Records Management will provide...in the records management team. The incumbent will ensure GCP compliance and inspection readiness related to… more
- Lifelancer (Minneapolis, MN)
- About the job Regional Associate Director , US Field Medical Cardiovascular - Central Region Job Title: Regional Associate Director , US Field Medical ... data generation, insight generation and patients' access to medicine. The Regional Associate Director (RAD) role is field-based and focused on managing… more
- Takeda Pharmaceutical Company Limited (Boston, MA)
- …learnt framework across CPMQ Provide expert guidance to the CPMQ team on quality compliance activities. Provide guidance and support to GCP , PV Health Authority ... Management and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . Advanced knowledge of pharmaceutical development, medical affairs and… more
- MannKind Corporation (Bedford, MA)
- …requirements and guidelines (FDA, EMA, PMDA, ICH, etc.), ensuring company compliance and best practices. Partner with cross-functional teams, including clinical ... managing multiple priorities in a fast-paced environment. Deep understanding of ICH- GCP guidelines and other relevant regulatory requirements. Strategic thinker with… more
- Lifelancer (London, KY)
- …and operational direction for ongoing clinical trials. Line manage a team of 2 Associate Directors and 1 Medica Director Lead the design, execution, and ... About the job Sr Medical Director Job Title: Sr Medical Director ...and safety risk mitigation across studies. Ensure adherence to ICH- GCP guidelines and regulatory compliance across all… more
- Alcanza Clinical Research (Roslindale, MA)
- …following according to study protocol, company processes & procedures, and in compliance with FDA, GCP /GDP/ALCOAC, ICH regulations and guidelines: a. Screening ... focus on enhancing efficiencies, facility management, patient safety and protocol/ GCP /SOPs/policy/regulatory compliance ; Collaborating with manager to support… more
- Alliance Clinical Network (West Hills, CA)
- …like to meet you. ESSENTIAL DUTIES AND RESPONSIBILITIES: Partner with Regional Site Director to ensure compliance and productivity of all clinical site staff ... disabilities to perform the essential functions. EDUCATION AND EXPREIENCE: Associate 's degree and/or completion of accredited healthcare certification program,… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Associate Director , Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is ... responsible for the effective management of GCP , GVP and GLP inspections. The GDQIM IML will...guidelines including the management of significant/complex quality issues and compliance activities. * Extensive experience with participating in, and… more
- Amgen (Washington, DC)
- …Suppliers for Amgen sponsored clinical trials + Monitoring and evaluating Supplier compliance and data quality + Tracking corrective actions in relation to ... external partners, including study teams, functional leads, procurement, quality, compliance , and suppliers + Support business functions with evaluation, selection,… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
- Takeda Pharmaceuticals (Boston, MA)
- …on quality compliance activities. + Provide guidance and support to GCP , PV Health Authority inspections including logistics. + Present insights to the health ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- We are seeking a Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the ... of study data of a clinical development program. The Associate Director leads in a matrix environment...compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Alliance Vendor Relationship Manager Date: Jul 22, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva ... and new people to make a difference with. **The opportunity** The Associate Director , Alliance/Vendor Relationship Manager will be responsible for managing… more
- System One (Tarrytown, NY)
- Job Title : Temp - Associate Director , Aggregate Reporting, GPS Type: Contract Compensation: $85 - $100 hourly (dependent on experience) Contractor Work Model: ... + Ability to interpret clinical data to support benefit-risk assessments. Temp - Associate Director , Aggregate Reporting, GPS + Submit Candidate + This position… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring ... and Statistics, with at least 3 years of experience in GCP Quality/ Compliance . + Advanced knowledge of pharmaceutical development, medical affairs and … more
- Wolters Kluwer (Tampa, FL)
- **Purchasing & Procurement Associate Director (Strategic Sourcing | Technology) - R0049352 USA** **| GBS | Sourcing - Wolters Kluwer** **Job Description** As a ... **Purchasing & Procurement Associate Director ** , you will lead complex...procuring technology-related services, including infrastructure and software (specifically hyperscalers GCP , AWS, and Azure). This experience should cover various… more
- Guidehouse (Boston, MA)
- …**Clearance Required** **:** None **What You Will Do** **:** We are seeking an experienced Associate Director to join our growing AI and Data practice, with a ... excellence, decarbonization goals, grid modernization, and customer-centric innovation. The Associate Director will oversee cross-functional teams and… more
- BeOne Medicines (San Mateo, CA)
- **General Description:** The Associate Director (AD), GCOE Learning and Development responsible for managing the governance, configuration, and optimization of ... as investigational sites. The role is accountable for maintaining training compliance across the clinical operations organization. This includes ensuring that… more
