- Actalent (Boston, MA)
- Job Description The Senior Clinical Trial Associate (Sr. CTA) is responsible for supporting the daily workflow of clinical operations activities. The Sr. ... document filing, maintaining study trackers, and oversight of the study-specific electronic Trial Master Files (eTMF). Responsibilities + Serve as a member of the… more
- Takeda Pharmaceuticals (Boston, MA)
- …direct the execution of diversity and inclusion strategy and tactics for global clinical trial programs. + Accountable for the co-creation and implementation of ... Clinical Operations staff on the importance of diversity in clinical trial populations. **Accountabilities:** + May be accountable for the leading the… more
- Actalent (Waltham, MA)
- …pharmacists, while contributing significantly to the management and execution of the clinical trial . CRAs will collaborate with other cross-functional team ... Clinical Research AssociateJob Description The in-house Senior Clinical Research Associate (CRA) performs a key...in this high-profile role. They will communicate regularly with Clinical Trial Managers (CTMs) regarding work progress… more
- Pfizer (Cambridge, MA)
- The Associate Director, Clinical Diagnostics will support...with Asset Teams to manage the timely testing of clinical trial samples and the analysis and ... flow cytometry + An understanding of translational approaches as applied to clinical trial design and regulatory processes, proof-of-concept studies, and the… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …The Associate Medical Director leads and drives strategy for clinical studies focused on neurodegenerative disorders within the overall global clinical ... that will inspire you and empower you to shine? Join us as an Associate Medical Director Neurodegenerative Disorders in our Neuroscience Therapeutic Area Unit in our… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …that will inspire you and empower you to shine? Join us as an Associate Medical Director, Clinical Science in our Gastrointestinal & Inflammation Therapeutic ... a vital contributor to our inspiring, bold mission **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for the overall global … more
- Cytel (Cambridge, MA)
- …behind you, you'll be at the heart of our client's innovation. The Associate Director, Clinical Data Standards proactively participates in the development of ... data and reporting standards in support of the client's portfolio of clinical trials and ensures conformance to CDISC standards and industry best practices. This… more
- Takeda Pharmaceuticals (Boston, MA)
- …of compliance management related to quality events and internal audits for clinical trial delivery functions including the identification and development of ... and empower you to shine? Join us as an Associate Director, GCP Compliance based remotely reporting to the...+ Establish and lead proactive risk-based compliance assessments for clinical trial delivery functions and ensure completion… more
- Dana-Farber Cancer Institute (Boston, MA)
- …document collection and maintenance compliance. + Assumes responsibilities for all clinical trial reporting requirements; safety event, annual approval, ... The CRM will be supervised and supported by the Associate Director of Cohort Studies to develop and implement...Will maintain per DFCI CTO standards. **DATA MANAGEMENT & CLINICAL TRIAL MONITORING:** + Responsible for development… more
- Novo Nordisk (Lexington, MA)
- …medicinal product dossiers (IMPD), investigational new drug applications (IND), clinical trial applications (CTA), marketing authorization applications (MAA), ... clinical development and regulatory requirements of a clinical program. The Associate Director will provide...Informed consent and assent forms + Lay summaries of clinical trial results + Clinical … more
- Astrix Technology (Boston, MA)
- …space. + Working knowledge of Clinical & Regulatory systems such as Clinical Trial Management System (CTMS), electronic Trial Master Files (eTMF), ... for the sale and growth of Astrix Technology Group's Clinical and Regulatory Consulting services to a portfolio of...representative of those that must be met by an associate to successfully perform the essential functions of this… more
- Takeda Pharmaceuticals (Boston, MA)
- …team, provides strategic planning, integrating, execution, build and oversight of clinical trial deliverables. CDCS leads the integration of collected ... and empower you to shine? Join us as an Associate Director, Data Configuration Engineer in our Cambridge, MA...products. Further, CDCS efforts enable valid secondary use of clinical trial data throughout Takeda research groups… more
- Harvard University (Cambridge, MA)
- …programming skills in a clinical data environment or research setting, preferably with clinical trial data + Proven skills in the use of SAS and a ... scripting language within a Statistical Programming environment preferably with clinical trial data (knowledge of R is desirable) + Strong team player that has a… more
- Dana-Farber Cancer Institute (Boston, MA)
- …of those cancer patients and their families undergoing therapy in a clinical research trial . Strong interpersonal, organizational and communication skills are ... with the physician, is responsible for the implementation and evaluation of clinical research in their specific program/area. The CRN has expert knowledge of… more
- Pfizer (Cambridge, MA)
- …communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results **,** ... biostatistics, or related field. + A minimum of 4 years' experience in the clinical trial setting (preferably in oncology of Pharma). + Relevant clinical … more
- Merck (Boston, MA)
- …and retention efforts to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study sites and identifies potential ... **Job Description** **Job Description:** The Regional Medical Scientific Associate Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease… more
- Merck (Boston, MA)
- …and retention efforts to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study sites and identifies potential ... **Job Description** **Role Summary** + The Oncology Regional Medical Scientific Director ( Associate RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic… more
- Sanofi Group (Cambridge, MA)
- …lives. **Major Duties and Responsibilities:** Provide support and leadership to the clinical trial study and/or project team on all relevant statistical ... we have a shared commitment to bring innovation and rigor to oncology clinical development. As Associate Statistical Project Leader, you will lead several… more
- AbbVie (Cambridge, MA)
- …substantial understanding of relevant therapeutic area required. + Knowledge of clinical trial methodology, regulatory requirements governing clinical ... will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational input… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …(GLP, GCP, GCLP, CAP/CLIA) and QC data to support primary, secondary, and exploratory clinical trial endpoints. The person in the role will support clinical ... development expert to support genomics-based biomarker assays/technologies to support the clinical development of novel therapeutics across a range of disease areas… more