- Tris Pharma (Monmouth Junction, NJ)
- Associate Director / Director , Analytical Research and DevelopmentMonmouth Junction, NJ Analytical Development, R&DDescriptionTris Pharma, Inc. ... our Monmouth Junction, NJ headquarters has an immediate need for an experienced Associate Director / Director , Analytical Research & Development. Job Title… more
- Merck & Co. (Rahway, NJ)
- …the R&D engine that drives our Company's biopharmaceutical business.Position Description: Associate Director , Finance Clinical Development Finance (CDF) is ... goals.Under the guidance of the Oncology Clinical Development Finance Director , the Finance Associate Director ...Alliance Management, Product Development Team (PDT) Leaders, and Clinical Study Managers regarding study budgets, site and… more
- Eisai, Inc (Jersey City, NJ)
- …If this is your profile, we want to hear from you. Job Summary The Associate Director , Medical Writing will be the designated Lead Medical Writer for multiple ... #LI-Remote Eisai Salary Transparency Language:The base salary range for the Associate Director , Medical Writing is from :149,200-195,800Under current guidelines,… more
- Merck & Co. (North Wales, PA)
- …/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... trial design and product labeling as it relates to the use of study results in US promotion.Maintain current awareness of evolving FDA regulations and… more
- Genmab (Plainsboro, NJ)
- …be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director acts as a statistical expert supporting the clinical development ... as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …promise of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Director of In Vivo Pharmacology as part of the Research & ... position will perform preclinical and IND-enabling in vivo pharmacology and toxicology studies to support pipeline programs. The ideal candidate will have knowledge… more
- Novo Nordisk Inc. (Omaha, NE)
- …strategic and priority Managed Markets accounts. Position reports to Field Director /Senior Field Director /Executive Director . Essential Functions ... duties: Provides monthly reports on scientific leadership activities to Field Director including budget expenditures as directed Records all activities within One… more
- Merck & Co. (Rahway, NJ)
- …position drives scientific planning, strategy and execution of Phase 1-4 clinical studies . Under the direction of the Program Lead, you will collaborate with ... global, cross-functional team members including clinical directors and study managers to lead/support clinical trial scientific activities in the Atherosclerosis &… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as a member ... and nonclinical documents for submissions, eg, clinical protocols and study reports, preclinical reports, investigator brochures, application summary documents, etc.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to Clinical Operations. Represents Clinical Development on Project Teams. Responsibilities Study Strategy: Provides the strategic direction to Biostats Data Mgmt & ... Reviews patient population and protocol compliance for consistency with study strategy; Develops biomarker strategy in collaboration with Translational Medicine/Clin… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to advance the existing pipeline (including companion diagnostic deals, combination studies , and ARO collaborations). This role will also support more complex ... projects, including those to acquire new product opportunities or technologies to augment our pipeline. This person is responsible for coordinating cross-functionally (eg with commercial, R&D, legal, IP, finance, supply chain, and other relevant functional… more
- Eisai, Inc (Raleigh, NC)
- …managing the entire transfer process, including Due Diligence, Feasibility Studies , Protocols/Reports, PPQ, PAI Readiness, and Quality System Oversight ... Implementation.Audit and Compliance: Maintain audit readiness, support regulatory inspections, manage complaints effectively, oversee change control, review metrics, and conduct annual product reviews. This also involves building effective quality systems and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. Summary Position leads complex studies in study design, statistical analysis and interpretation of results ... and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and Clinical TrialsAbility to extract configurable data fields from a study protocolProficient in FDA regulations supporting the submission of adverse events ... for post-marketing and investigative drugs. Understanding of global regulations preferredGood knowledge of Good Documentation PracticesEffectively manages shifting priorities; skillfully aligns resources as applicable to priorities that require immediate… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …or clinical studies to review and revise CSPs, ICFs, Clinical Study Reports (CSRs), and build and review Statistical Analysis Plans (SAPs) and statistical ... of minimum core product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned product(s)Authors… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …vendor selection criteria.- Problem solves and negotiates in most service types, studies , and programs- Responsible for the development and management of other ad ... hoc special projects as they arise through minimal supervision. Proactively predicts and prevents issues and conflicts; appropriately escalates as needed through excellent communication and presentation skills.Qualifications: Successful candidates will be able… more
- Merck & Co. (Rahway, NJ)
- …build and lead a team of TA dedicated global and regional directors and associate directors. The Executive Director , Value & Implementation (referred to as EDMA) ... Job DescriptionThe Executive Director , Value & Implementation (V&I), Global Medical and...real-world evidence data generation and coordinates local data generation studies with V&I Outcomes ResearchSupports the Investigator-Initiated Study… more
- Genmab (Plainsboro, NJ)
- …essential to fulfilling our purpose.The Role & Department As a Senior Programming Associate or Programming Manager, you will be in the Statistical Programming team ... making and reporting to health authorities. You will report to the Director , Programming, and work closely with Data Management, Clinical Programming, Statistics,… more
- University of Washington (Seattle, WA)
- …**The School of Public Policy & Governance has an outstanding opportunity for an Associate Director of Finance & Administration to join their team.** The Evans ... professionally within the school is reflected by being consistent with these values. The Associate Director of Finance & Administration is a pivotal role within… more
- Dana-Farber Cancer Institute (Boston, MA)
- …the oversight of analytic dataset generation for specific outcomes and translational research studies . The Associate Director , Data Analysis and Management ... main responsibilities overseeing data analysis for specific investigator outcomes and translational studies , the Associate Director will work collaboratively… more
Related Job Searches:
Associate,
Associate Director,
Associate Director Clinical Study,
Associate Director Study Management,
Associate Director Study Manager,
Associate Director Study Start,
Director,
Study,
Study Director