- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring ... functional compliance teams for regulations impacting Clinical , Safety and Clinical Pharmacovigilance Medical Quality (CPMQ) processes and procedures and… more
- Takeda Pharmaceuticals (Boston, MA)
- …in the business units and affiliates. + Ensure that the Global Quality Audit functions consider clinical research and pharmacovigilance regulated activities ... (Global Audit, Compliance and Commercial Quality ) on fit-for-purpose Key Quality Indicators (KQIs) and metrics relevant to clinical research and… more
- Parexel (Providence, RI)
- …the activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely ... other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study...(CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. +… more
- Parexel (Providence, RI)
- …the activities associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely ... other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study...(CSP) or ICH-GCP compliance issues to Local Management and/or Clinical Quality Management (CQM) as required. +… 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 ... true to the best of my knowledge. **Job Description** ** Clinical Data Engineering (CDE) at Takeda: ** Key to...clinical trials and to the delivery of high quality in a timely manner, which is eventually used… more
- Lilly (Boston, MA)
- …plans for clinical studies, managing CROs and vendors to ensure high- quality execution. + Lead internal clinical trial team meetings, tracking key ... patient-facing materials, and vendor plans). + Assist in maintaining a quality -focused clinical infrastructure by developing, revising, and implementing SOPs… more
- Takeda Pharmaceuticals (Boston, MA)
- …our strategic partners and other vendors to ensure the effective execution of the clinical studies on time, with high quality and within agreed budget. ... with our strategic partners and other vendors. + Represent Clinical Operations at the Global Program Team (GPT) and...the Global Program Team (GPT) and partner with Global Clinical Lead to lead the Clinical Sub… more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- **Job Summary** The Associate Director Controlled Substances, Quality Global Product Quality - API/DP is responsible for directing quality oversight ... standards. This role has global responsibility for directing clinical and commercial product quality to ensure global supply for Otsuka's patients. This role… more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial ... with biologics-specific GMP requirements. This role has global responsibility for directing clinical and commercial product quality to ensure global supply for… more
- Boston Health Care for the Homeless Program (Boston, MA)
- …week, Monday - Friday Union: None Union Name: None Patient Facing: Yes The Associate Medical Director of Medical Respite, in close collaboration with the Medical ... Director , is responsible for the daily clinical ...admission to medical respite; working closely with the Medical Director , Director and Associate Directors… more
- Beth Israel Lahey Health (Boston, MA)
- …and advocating for the health of patients, families, and communities. The Nursing Director for the Cancer Clinical Trials Office (CCTO) reports directly to ... nursing staff and coordinates nursing coverage for trials, including directly working on clinical trials. The Nursing Director is responsible for working with… more
- Takeda Pharmaceuticals (Boston, MA)
- …areas and the ability to partner closely with internal/external stakeholders to ensure the quality of the study build in the EDC system. + Collaborate with various ... of any integration. + Ensure accurate delivery of study build with quality deliverables per specification. Participate in the development, maintenance and training… more
- Takeda Pharmaceuticals (Boston, MA)
- …the development of scientific communications strategy and deliverables, the ** Associate Director , Scientific Communications Lead, Hematology** proactively ... preferably in life sciences, and excellent project management skills. The Associate Director , Scientific Communications Lead, develops and implements strategic… more
- Tufts Medicine (Boston, MA)
- ** Clinical Director of Women's Health & Longevity Program** **Tufts Medicine & Tufts University School of Medicine** **Location:** Greater Boston, MA **Position ... Tufts Medicine and Tufts University School of Medicine invite applications for the Clinical Director of Women's Health and Longevity Program, that would include… more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- The Associate Director , Scientific Communications manages the execution of the core scientific and medical communications strategy for the relevant therapeutic ... the Senior Director to ensure timely and compliant submission of high- quality abstracts, posters, and manuscripts in line with Good Publication Practices (GPP)… more
- Tufts Medicine (Boston, MA)
- …and Laboratory Medicine of Tufts Medical Center, Tufts Medicine, is seeking a full-time Associate Medical Director of the HLA Laboratory. The HLA Laboratory is ... The ideal candidate should have an MD and board certified in Clinical Pathology or other relevant medical specialty; non-physician doctoral clinical … more
- Otsuka America Pharmaceutical Inc. (Providence, RI)
- …needs and nutraceutical products for the maintenance of everyday health. As an Associate Director , Biostatistician, you will be a champion of Otsuka's culture ... responsible for providing statistical expertise/input in the drug development including clinical development plan and regulatory submission strategy. This is a… more
- Sumitomo Pharma (Providence, RI)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, clinical … more
- IQVIA (Boston, MA)
- ** Associate Technology Solution Sales Director -eQMS (SmartSolve) & Quality Consulting** The Associate Technology Solution Sales Director will focus ... promoting **electronic Quality Management System (eQMS - SmartSolve)** and ** quality consulting services** as part of the Go-To-Market (GTM) strategy. This role… more
- IQVIA (Boston, MA)
- ** Associate Creative Director , Copy** **Overview** Wanna know what's rare? An agency that believes people do their best work when they're happy. An agency that ... to be rare with us? We're currently seeking an Associate Creative Director to lead Copy operations...will ensure that our clients are satisfied with the quality of our creative work, the value of our… more