- 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
- GRAIL (Providence, RI)
- …+ MS or PhD with 10+ years of experience in regulatory, development, clinical affairs, quality , or program management within the IVD, medical device, ... and we are using the power of next-generation sequencing (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome… more
- Parexel (Providence, RI)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ... + Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators + Drive Quality Event (QE) remediation,… more
- Parexel (Providence, RI)
- …of experience will be required for the more senior roles of Senior Project Leader, Associate Project Director , and Project Director . To excel in this role, ... part of driving success for our clients and advancing clinical research projects. As a part of the Global...on time delivery within budget and to the highest quality with the goal to exceed client expectations Successful… more
- Commonwealth Care Alliance (Boston, MA)
- 082310 InstED-Medical Expenses **Position Summary:** Reporting to the CMO/Medical Director and Associate Medical Director of instED, the Virtual Medical ... and relays any essential follow-up needs to the care team via the instED Clinical Resource Center (CRC) team. This is a per-diem position with a minimum commitment… more
- 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
- 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
- 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 remotely reporting to the Head, Clinical Site Startup and Engagement Process Excellence and Delivery. At Takeda, we are transforming the… 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
- 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
- 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
- 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
- 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
- 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)
- …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
- 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
