- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... state-of-the-art technology and applying rigorous scientific and ethical standards.The Senior Director has primary responsibility for the planning and directing… more
- Merck & Co. (South San Francisco, CA)
- … studies ; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug ... Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine...stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to… more
- Genmab (NJ)
- …to have you join us!The RoleGenmab is currently seeking a Hematology Medical Science Liaison (MSL)/ Senior MSL (Sr. MSL) to be a part of an exciting opportunity of a ... sponsored trials (ISTs), from submission, review and approval, through study activation/completionCollaborate effectively and proactively establish working relationships with… more
- Merck & Co. (North Wales, PA)
- …include:Collaborating cross-functionally in the development of Protocol and related study materials (eg, ICF documents / amendments); Partners with the ... Study Manager on study deliverables.Ensuring CRF design supports data collection in alignment with the protocol in collaboration with Data… more
- Merck & Co. (Rahway, NJ)
- …and interprets results from clinical trials to meet objectives of the study protocol.- Independently applies and implements basic and complex techniques to these ... regulatory agencies, or individual investigators.Provides responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors,… more
- Eisai, Inc (Cincinnati, OH)
- …want to hear from you. Job Summary The Medical Science Liaison (MSL) / Senior Medical Science Liaison (Sr. MSL) is a field-facing representative of US Medical ... Maintain and demonstrate thorough and up-to-date knowledge of disease state, study methodology, clinical information, and product data.Demonstrate full knowledge of… more
- Genmab (NJ)
- …experience preferredDemonstrated experience authoring protocols, investigator's brochures, and clinical study reports. Senior level candidates should also have ... quality, and scientific integrity? At Genmab, we are seeking a passionate and experienced Senior Medical Writing Manager to help us tell the story of our science… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Summary: The Senior Director, Head of RBQM (Risk Based Quality Monitoring) sets the vision ... Indicators, and grouped variables for signal detection. Articulate to Study Team for appropriate site and study ...to Study Team for appropriate site and study level triage, actions, and rectifications.- Deliverables: Working with… more
- ACROBiosystems Inc. (New York, NY)
- …candidate drug screening and optimization, CMC development, preclinical and clinical studies , commercial production, and companion diagnostics. We are committed to ... encouraging cross-functional collaboration and continuous learning. Job Summary The Senior Sales Specialist will lead commercial activities in the...states of New Jersey and New York. As a Senior Sales Specialist, you will partner to contribute to… more
- Eisai, Inc (Los Angeles, CA)
- …is your profile, we want to hear from you. Summary: The MSL ( Senior Medical Science Liaison or Principal Medical Science Liaison) is a field-facing representative ... dots' and see the 'big picture' as it relates to the business. The Senior / Principal MSL brings relevant insights from the field on research developments, treatment… more
- Merck & Co. (San Diego, CA)
- …and pharmacodynamic biomarkers in immune-mediated diseases.Design and execute computational studies to elucidate molecular mechanisms of drug action (MoA), disease ... pathogenesis, and therapeutic response, leveraging multi-modal data in immunology.Either develop novel computational tools and algorithms or adopt cutting-edge and scalable computational biology and data science approaches to integrate muti-resolution (bulk,… more
- Merck & Co. (North Wales, PA)
- …research support for Oncology programs.- The position reports to the Senior Director responsible for Portfolio Real-world Evidence (RWE) in Oncology.- -Position ... objectivesTo design and execute real-world evidence studies , designed to demonstrate the value of new products in support of HTA, reimbursement, provider, payer and… more
- Merck & Co. (Rahway, NJ)
- …and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case ... Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for… more
- Merck & Co. (North Wales, PA)
- …with the Investigator Study Program Committee to evaluate outcomes research study protocols for studies in local markets.Supports affiliates to understand ... and gain input on research design and implementation of retrospective database studies , assessment of patient reported outcomes, epidemiological studies and… more
- Merck & Co. (North Wales, PA)
- …and programs.In collaboration with internal teams and external partners, designs studies ; authors study protocols; and develops measurement questionnaires, case ... Outcomes Research, and will support Pneumococcal Vaccines.Under the guidance of a senior leader, this position supports value evidence outcomes research plans and… more
- Eisai, Inc (Nutley, NJ)
- …hear from you. The Vice President/Head of Global Clinical Operations is a senior leadership role responsible for overseeing all aspects of clinical trial execution ... within a pharmaceutical or biotechnology company. This role ensures studies are conducted efficiently, within budget, and in compliance with regulatory standards.… more
- Merck & Co. (Rahway, NJ)
- …and accountable for establishing the timelines for clinical supply needs per study and providing the signal for sourcing, manufacturing, packaging, and distribution- ... develops mitigation strategies for review with clinical partners and senior leaders.- - Works directly in the SAP system...to establish a consolidated , visible forecast for all study product needs (Bulk Drug Product and Clinical Finished… more
- Merck & Co. (North Wales, PA)
- …and Global Regulatory Affairs.--The AVP provides leadership and direction through senior -level and first-line managers and statistical staff focused on end to ... and seamless cross-functional collaboration to deliver novel strategic program and study design, analysis strategy, and analysis results with highest quality. This… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …meetings. May serve as medical lead for select company-sponsored evidence generating studies /projects. Manages all medical aspects such as study document ... SummaryThe Director US Medical Affairs (USMA) Oncology, under the direction of the Senior Director, USMA Oncology (US Medical Affairs team lead for compound), is… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Budget; Establishes effective communication between CRO / vendors / AROAdditional non- study related activities: Occasional senior management interactions at ... to Clinical Operations. Represents Clinical Development on Project Teams.Responsibilities: Study Strategy: Provides the strategic direction to Biostatistics Data… more
