- Takeda Pharmaceuticals (Boston, MA)
- …position supports Takeda's mission by maintaining high standards of quality and compliance in clinical trials . **This role is located in Cambridge, MA and is ... Breach review board meetings. + Lead complex quality investigations impacting the clinical trial delivery systems. + Provide Quality Leadership for Serious… more
- Takeda Pharmaceuticals (Boston, MA)
- …quality are considered. + Enable a compliant quality system in safety and clinical trial delivery systems via CPMQ continual improvements projects. Actively ... my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is...represent in continual improvement projects, related to safety and clinical trial delivery in partnership with GDO,… more
- Takeda Pharmaceuticals (Boston, MA)
- …Reporting to the Head of Strategic Partnerships and Outsourcing, the Executive Director Clinical Partner Outsourcing (CPO) is a strategic leadership role ... and cost optimization, in support of efficient execution of clinical trials . The Head of CPO will...improvement + Strong understanding of GCP, ICH guidelines, and clinical trial regulations **ADDITIONAL INFORMATION** + The… more
- Actalent (Boston, MA)
- Job Title: Director of Clinical Trial Data QualityJob Description The Director of Clinical Trial Data Quality will be responsible for overseeing ... control of electronic Case Report Forms (eCRFs) and other Clinical Trial Management System (CTMS) data, while... clinical data management. + Strong understanding of clinical trials . Additional Skills & Qualifications +… more
- Bristol Myers Squibb (Cambridge, MA)
- …+ Serves as a primary source of medical accountability and oversight for multiple clinical trials + Manages Phase I/II studies, with demonstrated decision making ... Monitoring** + Serves as an independent Medical Monitor for clinical trials from Phase 1 through Proof-of-Concept... development strategy + Analyzing, interpreting, and acting on clinical trial data to support development +… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …of regulatory guidance for industry applicable to the design, analysis of clinical trials and process for regulatory submissions across difference regions ... that will inspire you and empower you to shine? Join us as Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge, MA office. Our Data and… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …company that will inspire you and empower you to shine? Join us as a Director , Quantitative Clinical Pharmacology Lead in our Cambridge, MA office. Takeda is a ... highly innovative treatments to patients. These scientists (from quantitative clinical pharmacology, statistics, programming, outcomes research and epidemiology, patient… more
- Beth Israel Lahey Health (Burlington, MA)
- …LMCP, and affiliated hospitals (Beverly, Addison Gilbert, Anna Jaques, Winchester). + **Expand Clinical Trials :** Develop and implement Phase 1 clinical ... not just taking a job, you're making a difference in people's lives.** Director of Cancer Research/ Clinical Hematologist - Burlington **Job Description:** **… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …stages to post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director , GCD is responsible ... refine a clinical development strategy. + Designing clinical trials for the purpose of meeting...integrity of the methodology and ensure the safety of clinical subjects. + Leading clinical trial… more
- Takeda Pharmaceuticals (Lexington, MA)
- …engineering functions + Perform safety reviews on device and combination products from clinical trials and from the field **Training Development:** + Design ... evidence-based product use training programs for patients, healthcare professionals, and clinical trial staff + Develop innovative instructional methodologies… more