- Takeda Pharmaceuticals (Boston, MA)
- …company to inspire you and empower you to shine? Join us as an Associate Director , GCP Excellence in Clinical Trials based remotely reporting ... to the Director , GCP Excellence in Clinical Trials. At...and inspections. + Develop, lead and oversee strategies for GCP quality and inspection plans, collaborating with… 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...Investigator Site Preparation Visits, in collaboration with the GD Quality Assurance (GDQA) team and other relevant functional groups.… 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, ... System (QMS). This role requires an in-depth knowledge of GCP and understanding of regulatory requirements applicable to the...requirements applicable to the conduct of clinical trials. The Associate Director , Quality will partner… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. **Position Overview:** The PR&D Quality System Associate Director provides critical leadership, oversight, and ... Quality System (QS) are well managed. The PR&D Quality System Associate Director partners...supervision. + Strong working knowledge of cGMP requirements and GCP regulations. + Strong leadership and teamwork skills. +… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ... 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)
- …is true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ... and Statistics, with at least 3 years of experience in GCP Quality /Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and … 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..., you will liaise with cross-functional teams to drive quality statistical planning, analysis, and reporting in support of… 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 ... that all safety reports received from any source are reviewed according to ICH- GCP guidelines, regulatory requirements and company SOPs and procedures. + Performs … more
- BeOne Medicines (San Mateo, CA)
- …with CTOMs; including but not limited to adherence to monitoring SOPs, GCP guidelines, country-specific regulations, and general quality and risk-based ... the performance and results of multiple related teams Supports SR Director to develops departmental plans, including business, production and/or organizational… more
- J&J Family of Companies (Spring House, PA)
- …America, Spring House, Pennsylvania, United States of America **Job Description:** ** Associate Director , Patient & Site Engagement, Oncology** **About Oncology** ... best talent for a **Patient & Site Engagement (PSE) Associate Director (AD) Oncology located Europe, or...documentation of recruitment development and implementation requirements to ensure quality standards are met. + Identify and provide Key… more
- WCG Clinical (Cary, NC)
- Associate Director , Project Management (Remote) **General...to develop new products and therapies to improve the quality of human health. It is our role to ... experience, skills, education, and geographic location. **JOB SUMMARY:** TheAssociate Director , Project Management is responsible for supporting hiring, onboarding,… 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 pharmacovigilance, CROs and other vendors to ensure high quality of deliverables to support drug development processes and...Management best practices required. - Additionally, strong knowledge of GCP , GDP, and 21 CFR preferred - 7 or… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …, Software Product Development, this REMOTE position is a Software Engineering (SWE) Associate Director for the MMS, Dispensing business (> $1B revenue) located ... function with the goal of increasing speed to market, quality of software products, and compatibility of portfolio with...Docker Swarm, etc) + Cloud management experience (AWS, Azure, GCP , etc) + Experience in automating software and deployment… 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 ... aspects of data management, from planning and coordination to execution and quality control. The successful candidate will be responsible for managing relationships… 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 ... : Establish and maintain best practices for data governance, data quality , and compliance with financial services regulations. **Stakeholder Management** : Engage… 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 ... with numerous stakeholders such as , Clinical Research Associates, Statisticians, Quality Assurance, and Regulatory Affairs to drive data excellence and enhance… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , PV Medical Surveillance Princeton, NJ, USA Req #435 Tuesday, February 11, 2025 Looking for a chance to make a meaningful difference in the ... The candidate should have knowledge of ICH/FDA/EU/MHRA guidelines for GCP , GVP, and Clinical and post-marketing Safety Reporting. +...Attention to detail with a highly consistent focus on quality . + Ability to analyze, and interpret scientific and… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …This individual is responsible for data management activities and decisions including quality , timelines and resources related to the conduct of clinical research ... studies in accordance with applicable regulations, ICH/ GCP regulations and company Standard Operating Procedures (SOPs) within assigned program(s). The PDML is a… more
- Takeda Pharmaceuticals (Boston, MA)
- …Excellence (DLE), Global Regulatory Affairs (GRA), Global Development Organization (GDO), Clinical Quality (CQA), and the PV & Medical Quality (PVMQ) functions. ... Social Digital Media, and Market Research/Patient Support Programs (MR/PSP) processes. Quality metrics for Individual Case Safety Reports (ICSR), Agregate Safety… more
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