- Merck (Columbus, OH)
- **Job Description** The Senior Director, GCTO Project Management Office will report to the Executive Director, Head of the GCTO Project Management Office (PMO). You ... Build and maintain strong relationships with key stakeholders, including senior leaders, business area contacts, and project teams. Effectively communicate… more
- Bristol Myers Squibb (Princeton, NJ)
- …professional who has a strong proficiency in the curation and analysis of clinical trial intelligence data and its application to effectively conduct study ... and the creation/maintenance of data-driven patient recruitment and enrollment forecasts for clinical trial (s) within a clinical research development… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Trial Physician, Rheumatology sits within Cell Therapy ... point of expertise in key Health Authority interactions and advisory board meetings as Senior Clinical Trial Physician + Authors/drafts clinical content… more
- AbbVie (North Chicago, IL)
- … trial notifications etc. + Review of and input into documents related to clinical trial submissions managed by other stakeholders such as IB and Protocols. + ... operational support as required to the CTS managers / senior managers. Major Responsibilities + Operational support to CTS...with internal/external processes. + Provide operational support for the Clinical Trial Strategy & Submissions team. +… more
- Lilly (Indianapolis, IN)
- …Assurance (QA) is responsible for providing quality oversight of all materials used in clinical trials. PRD QA Clinical Trial (CT) Packaging is responsible ... for global packaging operations and provide on-going Quality oversight to outsourced Clinical Trial Packaging activities. The Packaging CP Oversight role is… more
- Bristol Myers Squibb (Princeton, NJ)
- …point of expertise in key Health Authority interactions and advisory board meetings as Senior Clinical Trial Physician + Authors/drafts clinical content ... as a primary source of medical accountability and oversight for multiple clinical trials + Matrix management responsibilities across the internal and external… more
- Merck (West Point, PA)
- … teams and in other trial -level development forums. Under the guidance of more senior staff, may serve as the data management lead or perform a support role for ... for trials as assigned. Under the guidance of more senior staff when appropriate, uses excellent interpersonal, negotiating, and...requirements for quality data collection and validation at the trial level. + Reads and interprets the clinical… more
- MD Anderson Cancer Center (Houston, TX)
- …of key functions. . Attend departmental or institutional research meetings. ** Clinical Trial Initiation & Multi-Center Coordination** . Under supervision ... submission and revisions. Develop research documents and tools to aid in meeting clinical trial requirements. . Support principal investigators and study teams… more
- Walgreens (Deerfield, IL)
- **Job Description:** **Job Summary** The Senior Manager Biostatistics will generate Clinical Trial and Real World Evidence (RWE) from various study designs ... for market access expansion. This role supports RWE and clinical trial study delivery, working cross functionally...ID:** 1345491BR **Title:** Senior Biostatistics Manager, RWE Clinical Trials - Remote **Company Indicator:** Walgreens… more
- Stryker (Cary, IL)
- …annually. More information is available at www.stryker.com We are currently seeking a ** Senior Clinical Study Manager** , to join our **Medical** Division. This ... regulations and expectations. **What you will do** As a Senior Clinical Study Manager, you will assume...+ Support development and maintenance of systems (eg, electronic trial master file (eTMF), clinical trial… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The role of Senior Clinical Program Leader (CPL) - Retinal health, assumes full medico-scientific and strategic leadership of clinical ... and other contributors), Clinical Development Plans or similar documents, Core Clinical Trial Protocols, including the CTP strategy and core CTP elements… more
- Stryker (Fremont, CA)
- …Check Specifications. + Develop complex status reports, specifications for analysis of clinical trial data for interim and final reports, training materials, ... award-winning organization by visiting stryker.com We are seeking a ** Senior Staff Clinical Data Manager** to join...databases are in accordance with internal and external established clinical trial and regulatory standards, and local… more
- Amgen (Thousand Oaks, CA)
- …drug development (population PK, mechanistic PK/PD modeling/systems pharmacology, and clinical trial simulations). Experience in design, interpretation, ... time for a career you can be proud of. ** Clinical Pharmacology, Modeling & Simulation- Senior Principal...and bi-annual company-wide shutdowns + Flexible work models, including remote work arrangements, where possible **Apply now** **for a… more
- Merck (Columbus, OH)
- …and ensures continuity of site relationships through all phases of the trial . + Performs clinical study site management/monitoring activities in compliance ... as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and… more
- Edwards Lifesciences (Newark, NJ)
- …modify clinical databases, and tools and programs for data validation checks, and clinical trial reporting + Lead cross functional teams in the design and ... specifications, reports and other database-related tasks during the life of a clinical trial to ensure data quality and compliance with regulatory guidelines and… more
- AbbVie (North Chicago, IL)
- …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Senior Manager, Clinical Data and Reporting Standards (CDARS) proactively ... and reporting standards in support of AbbVie's portfolio of clinical trials and ensuring AbbVie's conformance to CDISC standards...to CDISC. + Review and provide feedback on SDTM Trial Design Domains + Oversee the creation of SDTM… more
- GE HealthCare (Boston, MA)
- …The QA Auditor is responsible for ensuring that all aspects of the clinical trial comply with relevant regulations, guidelines, and standard operating procedures ... **Job Description Summary** The Good Clinical Practice (GCP) Senior Quality Assurance...Execution: They plan, conduct, and report on audits of clinical trial activities, sites, and documents to… more
- Edwards Lifesciences (Sacramento, CA)
- …* Develop and manage clinical project plans to identify and complete clinical trial milestones with accountability for successful completion of all project ... and be part of our inspiring journey. As the Senior Manager of Clinical Project Management, you...and SOPs. Serve as the primary lead of assigned clinical trial (s) * Provide direction, guidance, and… more
- Vitalief (New Brunswick, NJ)
- …is carried out as outlined. + Develops and distributes monthly financial reports to senior leadership of clinical trial revenue activity including active ... is responsible for preparing, maintaining, and negotiating budgets related to clinical trial activities. + Performs prospective reimbursement analysis according… more
- J&J Family of Companies (Columbus, OH)
- Senior Clinical Research Associate - 2406171534W **Description** Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Clinical ... day-to- day aspects of investigational site activities on assigned clinical trials. The Senior Clinical ...for internal and external audits to ensure all essential clinical Trial Master File (TMF) documents are… more