- 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
- Takeda Pharmaceuticals (Boston, MA)
- …and specialty data for the purposes of data modelling, simulation, and analysis. ** Associate Director , Clinical** **Data Engineer (CDE)** Key to Takeda's success ... Takeda's clinical trials and to the delivery of high quality in a timely manner, which is eventually used...Adhere to SOPs for computer system validation and all GCP (Good Clinical Practice) regulations + Performs clinical data… 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
- Bristol Myers Squibb (Princeton, NJ)
- …your application should be directed to Chat with Ripley. R1597973 : Associate Director , Companion Diagnostics & Bioanalysis **Company:** Bristol-Myers Squibb ... program needs require it. The incumbent will wire in quality from the start, embedding QMSR/820 design controls, CLIA/CAP,...of FDA QSMR, GLP, CLIA, CAP, ISO13485, IVDR, and ICH- GCP . + Experience with LIMS and electronic data management… more
- Bristol Myers Squibb (Princeton, NJ)
- …of your application should be directed to Chat with Ripley. R1595700 : Associate Director , Data and Solution Architect Revenue Management Systems **Company:** ... Management (MDM) and Data Governance, Metadata management and data lineage, Data quality , security, and privacy best practices. + **Cloud Platforms & Services:**… 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
- Morehouse School Of Medicine (Atlanta, GA)
- …playbooks, and feasibility/site-readiness tools aligned to policies approved by the CRC Associate Director and Quality /Compliance Core. * Track ... to ensure operations adhere to institutional policies, ICH - GCP , FDA / OHRP regulations, and payer rules....training on operational billing practices (policy ownership resides with Compliance/ Associate Director ). Regulatory & Quality … more
- Lilly (Boston, MA)
- …close-out, ensuring adherence to timelines, budgets, and regulatory guidelines (FDA, EMA, GCP , ICH) using a risk-based approach. + Develop and implement operational ... plans for clinical studies, managing CROs and vendors to ensure high- quality execution. + Lead internal clinical trial team meetings, tracking key study metrics (eg,… more
- Takeda Pharmaceuticals (Boston, MA)
- …to ensure the effective execution of the clinical studies on time, with high quality and within agreed budget. **ACCOUNTABILITIES:** + Accountable to the GPT for the ... research, including but not limited to US CFR, EU CTD, and ICH GCP . Awareness of local country requirements is also required. **Skills:** + Demonstrated excellence… more
- Astellas Pharma (Northbrook, IL)
- …and site management related activities according to agreed timelines and quality standards, including identifying areas for additional training and development + ... expertise in risk-based monitoring strategies and strong knowledge of ICH/ GCP guidelines and multinational clinical trial regulations + Must have experience… more