- Terumo Neuro (Aliso Viejo, CA)
- **13125BR** **Title:** Associate Director , Clinical Research (US Remote) **Job Description:** Lead the strategic planning and operational execution of clinical ... Hiring Ordinance, and San Francisco Fair Chance Ordinance. **External-Facing Title:** Associate Director , Clinical Research (US Remote) **Posting Country:** US… more
- WCG Clinical (Cary, NC)
- Data Analytics & Insights (DAI) Product Solutions, Associate Director (Remote) **General Information** **Location:** Cary, NC, Remote **Organization:** ... to develop new products and therapies to improve the quality of human health. It is our role to...and geographic location. **JOB SUMMARY:** The DAI Product Solutions Associate Director is a key leader responsible… more
- Parexel (Montpelier, VT)
- …associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading ... other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study...GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. + Assists site in… more
- Parexel (Juneau, AK)
- …to safeguard the quality of investigator sites (eg patient safety, site quality and compliance with GCP ), to maintain investigator and site staff engagement ... **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site...clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws,… more
- Parexel (Columbia, SC)
- …associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading ... other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study...GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. + Assists site in… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** **ABOUT THE ROLE** The Associate Director , GCP Audit & Compliance provides strategic quality oversight to clinical, medical, ... field (or equivalent). + Minimum 15+ years of experience in GCP /GCLP/GVP Quality or Compliance within the pharmaceutical industry. + Advanced understanding of… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process 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
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Associate Director , Regulatory Job Profile Title Associate Director , ... Clinical Research Regulatory Job Description Summary With the oversight of the Director , the Associate Director for Regulatory Affairs will oversee the… more
- Humana (Baton Rouge, LA)
- …a part of our caring community and help us put health first** The Associate Director of Cloud Infrastructure Operations is responsible for leading Humana's ... transformation at the intersection of operations, technology, and AI innovation. The Associate Director of Cloud Infrastructure Operations will drive the… more
- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. The Associate Director , ICSR Management Team reports to the Director , Head, ICSR ... in the safety database and are reported according to ICH- GCP guidelines, Healthy Authority regulations and company SOPs, Work...PV Vendor processing ICSRs for Ascendis Products. + Performs Quality Checks of processed ICSRs and provides feedback to… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …outsourcing, oversight and risk-based data management strategies, standards and processes. The Associate Director , Data Management will bring deep knowledge of ... management strategies, processes, and standards in alignment with Good Clinical Practices ( GCP ) and applicable regulatory guidelines (eg, FDA, EMA, ICH). * Oversees… more
- ThermoFisher Scientific (Las Vegas, NV)
- …includes a drug screening. Due to continued growth, we are looking to appoint an Associate Medical Director at the Las Vegas Clinical Research Unit. This role is ... an office-based position for a motivated Physician. The Associate Medical Director serves as the physician...being conducted under all applicable laws, regulations and per ICH- GCP guidelines in the organization's Clinical Research Unit (CRU).… more
- Takeda Pharmaceuticals (Boston, MA)
- …company to inspire you and empower you to shine? Join us as an Associate Director , Clinical Site Startup and Engagement Process Excellence & Delivery based ... of new/updated processes and technologies are in compliance with quality standards (including ICH, GCP , local regulations and Takeda SOPs). + Ensure that crucial… more
- Philips (Cambridge, MA)
- …of our talented Hospital Patient Monitoring (HPM) Clinical Affairs team, the Associate Director - Clinical Operations, is responsible for day-to-day Clinical ... Management and providing expertise in clinical research process legislation, ICH- GCP guidelines, improving efficiency in clinical execution. **Your role:** +… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and Metabolism (ExpMed - CRM) is currently seeking a talented and innovative Senior Associate Director , Clinical Trial Leader to support our ExpMed team to join ... field from start of development (SoD) to proof of concept (PoC). The (Senior) Associate Director , Clinical Trial Leader (AD, CTL) is accountable for the set-up,… more
- Carrier (Palm Beach Gardens, FL)
- …or follow Carrier on social media at @Carrier. **About This Role** The Associate Director of Network Operations is responsible for guiding the strategic ... operations. As a pivotal member of the network management team, the Associate Director will provide thought leadership and collaborate with engineering… more
- System One (Princeton, NJ)
- Job Title: Associate Director of IT - Life Sciences/Clinical Location: Princeton, NJ (Mostly remote with some onsite collaboration required - only EST candidates ... Strong understanding of CDISC standards, 21 CFR Part 11, GCP , and system validation. + Demonstrated ability in change...get work done more efficiently and economically, without compromising quality . System One not only serves as a valued… more
- IQVIA (Boston, MA)
- **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director /Trial Delivery Manager (TDM) to lead and coordinate global ... and interfacing with internal and external stakeholders to ensure compliance, quality , and timely delivery of trial milestones. **Key Responsibilities:** **Trial… more
- J&J Family of Companies (Cambridge, MA)
- …at https://www.jnj.com/innovative-medicine **We are searching for the best talent for an Associate Director , Global Proteomics to be located in Cambridge, MA.** ... presentations). + Knowledge of **fit** **‑** **for** **‑** **purpose quality systems** (eg, GLP‑adjacent discovery practices), laboratory information management… more
- Pfizer (Bothell, WA)
- **JOB SUMMARY** The **A** **ssociate** ** Director , Oncology Biometrics** is a skilled biostatistician who can work independently as the study statistician for Phase ... 1-2 studies and under the direction of a Director of Biostatistics, or above, as the study statistician...data analysis strategies to meet project objectives with high quality in a timely manner. * Provide statistical inputs… more
