- 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
- Takeda Pharmaceuticals (Boston, MA)
- …Senior Manager, GCP Excellence in Clinical Trials based remotely reporting to the Associate Director , GCP Excellence in Clinical Trials. At Takeda, we ... departmental objectives, representing GCP Excellence globally. Develop and implement GCP Excellence processes to enhance support and compliance , identifying… 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
- Lilly (Indianapolis, IN)
- …for people around the world. **Position Overview:** The PR&D Quality System Associate Director provides critical leadership, oversight, and cross functional ... the PR&D Quality System (QS) are well managed. The PR&D Quality System Associate Director partners cross functionally with the business to implement key… more
- Takeda Pharmaceuticals (Boston, MA)
- …delivery, and deployment of training; monitors and tracks employee training compliance with the LMS. + Oversees the coordination, including the collection, ... tracking, and trending of key PV Compliance metrics for the monthly cross-functional Compliance ...of FDA/EU regulations, and ICH guidelines for GVP and GCP with practical experience in the interpretation and implementation… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Join Gilead and help create possible, together. **Job Description** **Summary** The Associate Director , Quality will be responsible for designing, implementing, ... requirements applicable to the conduct of clinical trials. The Associate Director , Quality will partner with key...CDS organization to ensure clinical trials are conducted in compliance with Gilead procedures, GCP and applicable… more
- Bristol Myers Squibb (Summit, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Therapeutic Area Audit Strategy Lead will be ... the central QMS team + Lead the Quality and Compliance R&D Escalation Process + Ensure GLP systems are...of vendors and manage external Quality Systems + Execute GCP and Pharmacovigilance audits and support GCP … more
- IQVIA (Durham, NC)
- **Job Level: Associate / Director of Biostatistics,** **Early Phase Pharmacodynamics** **Location:** **Home-based in the US or Canada** **(East Coast Preferred)** ... **Job Overview:** As an ( Associate ) Director , you will liaise with cross-functional...resource for the department, ensuring scientific integrity and regulatory compliance in the application of statistical methodology to clinical… more
- Ascendis Pharma (Palo Alto, CA)
- …a dynamic workplace for employees to grow and develop their skills. The Associate Director , Global Pharmacovigilance Operations reports directly to the Head of ... of CAPAs as necessary + Work Closely with Ascendis GCP /PV Compliance team and Commercial organization as...team (specifically from: Talent Acquisition Partner or Human Resources Director ) is not allowed. If this occurs your ownership… more
- J&J Family of Companies (Titusville, NJ)
- …https://www.jnj.com/innovative-medicine **We are searching for the best talent for an Associate Director , Portfolio Lead Clinical Programming within C&SP Group ... to be located in Titusville, NJ.** **Purpose:** An Associate Director , Portfolio Lead is a highly experienced individual with expert understanding of programming… more
- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. Associate Director , Global Patient Safety Medical Science reports to Head of GPS ... of products in development. + Through coordination with Ascendis GCP and PV Compliance team will provide...team (specifically from: Talent Acquisition Partner or Human Resources Director ) is not allowed. If this occurs your ownership… 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
- Lilly (Stamford, CT)
- …make life better for people around the world. **Position Summary** : The Associate Director , Clinical Development Trial Lead (CDTL) independently leads the ... trial(s) with quality, on time, and within scope and budget. The Associate Director , CDTL consistently demonstrates independent leadership, influence when… more
- IQVIA (Durham, NC)
- …in the US or Canada** **(East Coast Preferred)** **Job Overview:** As an Associate Director , you will liaise with cross-functional teams to drive quality ... **Job Level: Associate / Director of Biostatistics,** **Rare Disease, FSP**...resource for the department, ensuring scientific integrity and regulatory compliance in the application of statistical methodology to clinical… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …areas centered around rare diseases and immune disorders. **Summary:** The Associate Director , Data Management Processes, Training and Inspection Readiness, ... and/or implement any changes that are required to department training, compliance , or operations. Ensure appropriate Data Management representation and contribute to… more
- OneMain Financial (Irving, TX)
- …actionable insights into digital behaviors and performance. We are seeking an experienced Associate Director of Data Products to lead our shared data products ... and maintain best practices for data governance, data quality, and compliance with financial services regulations. **Stakeholder Management** : Engage with senior… more
- Bristol Myers Squibb (San Diego, CA)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals . **Summary:** The Associate Director , Clinical Data Management, will play a crucial role in ... as needed. + Contribute to SOP development and updates to meet regulatory compliance and operational needs. + 10% of travel required. **Basic Qualifications:** +… more
- Merck (Rahway, NJ)
- **Job Description** **Job Overview:** We are seeking a highly qualified and experienced Associate Director in Data Management to lead our data management team in ... Proficient in database entry systems. + Strong knowledge of GCP and GLP. + Thorough understanding of clinical research...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance **Los… more
- Merck (Rahway, NJ)
- …+ Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. **Preferred Experience and Skills:** + Proficiency in using ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance **Los Angeles Residents… more
- e CancerCare (Fresno, CA)
- Purpose: The Director , Clinical Trials & Research, for CCARE Physicians, PC, is responsible and accountable for the daily operations and management of staff, of the ... the finance department, the overall financial activities of the department. Assures compliance with all regulatory requirements and standards of good practice (… more
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