- Eisai, Inc (Nutley, NJ)
- …make a difference. If this is your profile, we want to hear from you. Associate Director , Medical Education - Oncology, is responsible for the strategic planning ... & ManagementEisai Salary Transparency Language:The base salary range for the Associate Director , Medical Education - Oncology is from :162,600-213,400Under… more
- Genmab (NJ)
- …to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading the development and ... and/or intelligence deliverables. This role will be within Global Regulatory Affairs (GRA) and will report to...Affairs (GRA) and will report to the Sr. Director , Labeling, Policy and Intelligence. The position may be… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …is a global role that will cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the ... (eg SOPs) as appropriate.Collaborate with cross-functional teams (eg, Medical Safety, Regulatory Affairs , Epidemiology) to ensure benefit-risk integration to… more
- Insmed Incorporated (San Diego, CA)
- …for Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director , EDC Programming will lead and oversee EDC ... with the Biometrics teams, Clinical Operations teams, Clinical Development teams, Regulatory Affairs , and external partners.ResponsibilitiesEDC System Design &… more
- Merck & Co. (Upper Gwynedd, PA)
- …and development through information science. We are seeking a passionate, experienced Associate Director to connect scientists and stakeholders with focused ... alerts and knowledge services that empower research teams across the organization.As Associate Director , you will collaborate closely with cross-functional teams… more
- Lupin Pharmaceuticals (Coral Springs, FL)
- …profile (TPP) development, due diligence projects, and clinical- regulatory compliance. ResponsibilitiesEssential Duties and Responsibilities Clinical Development: ... execute clinical trials for respiratory products, ensuring compliance with regulatory requirements.Collaborate with cross-functional teams to develop study protocols,… more
- Merck & Co. (Millsboro, DE)
- …SOPs, Quality Notifications and technical documentation; collaborate cross-functionally with QA, Regulatory Affairs , EHS, Engineering, BTS, ATS and HR.Direct ... operations, formulation and fill/finish activities.Ensure compliance with corporate and regulatory requirements (cGMP/USDA) and lead IPT support for audits,… more
- Merck & Co. (Upper Gwynedd, PA)
- …--Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice...Medical Research, Mentorship, Plan of Action and Milestones (POA&M), Regulatory Affairs Compliance, Regulatory Compliance… more
- Monster (Bernards, NJ)
- …is a global role that will cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the ... SOPs) as appropriate. Collaborate with cross-functional teams (eg, Medical Safety, Regulatory Affairs , Epidemiology) to ensure benefit-risk integration to ensure… more
- Merck & Co. (Rahway, NJ)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.- Specifically, the Senior Director … more
- Programmable Medicine Operatin (Redwood City, CA)
- …meetings with Clinical Operations, Clinical, Clinical Supply Chian, Quality Assurance, and Regulatory Affairs Responsible for drug substance and drug product and ... options. The Company also offers participation in the annual bonus program. At the Associate Director level, the salary range for this position is $160,000 -… more
- Merck & Co. (Boston, MA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the timely deployment of CDx assays that are compliant with applicable global regulatory guidelines. Collaborates wtih Regulatory Affairs to develop CDx ... trials or for approval of CDx. Keeps abreast of regulatory and policy updates in the external environment and...strategy to account for external shifts. Partners with Medical Affairs and Commercial to support scientific collaborations with KEEs,… more
- City of Canby, OR (Canby, OR)
- …Position Overview The City of Canby is recruiting to fill the role of Finance Director . The ideal candidate will bring a positive energy to the City while providing ... and reports are in compliance with all appropriate legal and regulatory requirements and Generally Accepted Accounting Principles for municipal agencies. Establish… more
- Monster (Bernards, NJ)
- …the timely deployment of CDx assays that are compliant with applicable global regulatory guidelines. Collaborates wtih Regulatory Affairs to develop CDx ... interactions for the drug trials or for approval of CDx.Keeps abreast of regulatory and policy updates in the external environment and understands the competitive… more
- Health eCareers (Edison, NJ)
- …leader in graduate medical education (ie, successfully holding a position as a GME program director or Associate Director or Director of Medical ... Education (GME) programs, ensuring the highest standards of academic excellence and regulatory compliance.As the ACAO, you will be a key leader in implementing… more
- JENAVALVE TECHNOLOGY INC (Irvine, CA)
- …Description Summary: The Senior Clinical Research Associate will report to the Associate Director , Clinical Programs, and will play a key role in proactively ... Salary Range $85000.00 - $110000.00 Salary Description Job Title: Senior Associate , Clinical Research Supervisor/Manager Title: Senior Manager, Clinical Affairs … more
- Health eCareers (Hartford, CT)
- …improvement (CDI). You will report directly to the Senior Vice President of Medical Affairs /CMO and a System Lead Director for Care Management and Documentation ... health system, is seeking an experienced Board-Certified physician leader to be Associate Chief Medical Officer at Saint Francis Hospital and Medical Center in… more
- CoxHealth (Springfield, MO)
- …service agreement terms and conditions. This position will also assist the Regulatory Affairs department with annual contract evaluations. The Contracted ... industry standards. This position will report to the Biomedical Equipment Services Director . Job Requirements Education Required: Associate or related Degree in… more
- Abbott (Santa Clara, CA)
- …the medical device business units that Leveraged Services team supports. **The Opportunity** The ** Associate Director Regulatory Affairs ** will work for ... Drug Administration (FDA) Center for Devices and Radiological Health (CDRH). This Associate Director Regulatory Affairs may analyze broad scope… more
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