- AbbVie (North Chicago, IL)
- …LinkedIn. Job Description Purpose: The primary responsibility of the AMD, Innovative Trial Designs, Immunology is to support the overarching safety strategy for ... interactions regarding safety monitoring in the planning of innovative trial design protocols (eg implementing stopping rules, appropriate mitigation measures,… more
- AbbVie (New York, NY)
- …clinical trial populations. This role will report into the Associate Director, Diversity & Patient Inclusion. Responsobilties: + Drive the strategic ... customer-centric solutions with patients and sites that enable equitable trial access and enhanced trial experiences. The...applying to a position in any location with pay disclosure requirements under state or local law: … more
- AbbVie (Chicago, IL)
- …YouTube and LinkedIn. Job Description The Manager of the Clinical Trial Strategy and Submission delivers clinical development regulatory strategies & operations ... accordance with global regulatory strategies and compliance with evolving global clinical trial legislation (including the EU Clinical Trial Regulation, IVDR,… more
- AbbVie (Branchburg, NJ)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director, Clinical Development will have global or regional responsibilities and ... Clinical Program Lead and Clinical Science Lead and Clinical Scientist. The Associate Director, Clinical Development should expect to be asked to participate in… more
- Takeda Pharmaceuticals (Columbus, OH)
- …**How you will** **contribute:** + Oversee and direct the work of the Clinical trial disclosure programming team (within the Programming Center of Excellence) in ... and external presence on varied statistical programming topics. + Support Clinical Trial Disclosure Programming and data anonymization. + Provides technical… more
- Hartford HealthCare (Bridgeport, CT)
- …*Job Summary:* As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal Investigator (PI) in leading all ... primarily responsible for the overall design, conduct, and management of the clinical trial , the SrCRA leads, facilitates and coordinates all clinical trial … more
- AbbVie (North Chicago, IL)
- …implement translational strategies to advance AbbVie's innovative Oncology pipeline. The Associate Director, Biomarker Program Management, leads a team within the ... quality and efficiency, on-time, within budget, and meet objectives. The Associate Director achieves these objectives via scientific expertise, strategic thinking, a… more
- Randstad US (Newbury Park, CA)
- sr associate clinical contracts & budgets. + newbury park , california (remote) + posted august 28, 2024 **job details** summary + $30 - $75 per hour + contract + ... associate degree + category life, physical, and social science...to end process for clinical site contracts and clinical trial related consulting agreements (including contracts, amendments and termination… more
- AbbVie (North Chicago, IL)
- …the program level consistency and an enabler of the operational team supporting trial execution. This role is a highly empowered leader, influencer across the ... functions within DSS and Development and a contributor to trial planning, design, and flawless execution. + Overall owner...applying to a position in any location with pay disclosure requirements under state or local law: … more
- National Geospatial-Intelligence Agency (Springfield, VA)
- Summary Associate General Counsel for Legal Operations and Business Management Responsibilities BASIC DUTIES AND RESPONSIBILITIES: Serves as the Senior Associate ... NGA. Designated as senior by position to the NGA Associate General Counsels and serves as principal Agency legal...is subject to the completion of a one-year DISL trial period. (Applicants selected from outside NGA may be… more
- AbbVie (Mettawa, IL)
- …will be determined by the qualifications listed below. Purpose: The Associate Scientific Director, Psychiatry Pipeline role provides medical and scientific strategic ... at the regional/local level. + Participation in design and execution of clinical trial safety, product safety and risk management plans. Responsible for routine and… more
- AbbVie (Newark, NJ)
- …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director, Patient Experience Data (PED) Policy & Best Practices, is ... for AbbVie in alignment with external policy and scientific advancements. The Associate Director, PED Policy & Best Practices, will cultivate strong partnerships… more
- Pfizer (Collegeville, PA)
- …statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results **,** support for ... A minimum of 4 years' experience in the clinical trial setting (preferably in oncology of Pharma). + Relevant...of payments or other value received, generally for public disclosure . Subject to further legal review and statutory or… more
- AbbVie (Mettawa, IL)
- …Facebook, Instagram, YouTube and LinkedIn. Job Description Purpose: The Associate Scientific Director provides medical and scientific strategic and operational ... materials. + Participates in design and execution of clinical trial safety, product safety and risk management plans. Track...applying to a position in any location with pay disclosure requirements under state or local law: … more
- AbbVie (North Chicago, IL)
- …and responses, and other program documents. *May oversee the work of Associate Medical and/or Scientific Directors, and of Clinical Scientists working on the ... is desirable. + At least 0-2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent....applying to a position in any location with pay disclosure requirements under state or local law: … more
- AbbVie (North Chicago, IL)
- …+ Strong desire to collaborate in a cross-functional setting. + Clinical trial experience in the pharmaceutical industry, academia, or equivalent is preferred. + ... Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials...applying to a position in any location with pay disclosure requirements under state or local law: … more
- AbbVie (North Chicago, IL)
- …and stability studies to establish clinical product dating; substantial clinical trial application submission content. Section I: Major Responsibilities + Analytical ... characterization and assessment of process/formulation development samples and clinical trial supplies (eg GMP compliant stability and release testing) + Provide… more
- AbbVie (Durham, NC)
- …for conducting and delivering fit for purpose analysis related to clinical trial feasibility including, study design, study benchmarking, country and site selection ... and leadership competencies + Advanced domain knowledge in clinical trial feasibility and real-world data sources + Experience in...applying to a position in any location with pay disclosure requirements under state or local law: … more
- AbbVie (Mettawa, IL)
- …will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational input ... standards, including regulatory guidelines to meet customer needs. Qualifications Associate Scientific Director Qualifications + Bachelor's Degree in the sciences.… more
- Pennsylvania State University (University Park, PA)
- …. JOB DESCRIPTION AND POSITION REQUIREMENTS: Part-Time Junior Policy Associate : Paid Internship to Implement a BIPOC Policy Scholars Program ... anticipate this individual would support on implementation activities related to the trial of the Research-to-Policy model. This includes: + Implement the BIPOC… more