- Merck & Co. (Upper Gwynedd, PA)
- … Senior Director will manage the entire cycle of clinical development, including study design, initiation, execution,- monitoring, analysis, regulatory reporting, ... trials and will interact externally with key opinion leaders. Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and translational… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAs a Senior Engineer in Device Design and Process Development group, you will be part of our Research & Development team that designs and develops ... benchtop/low-volume to high-volume clinical and commercial assembly equipment and processes for medical devices/drug delivery systems. Reporting to the Director… more
- Merck & Co. (Rahway, NJ)
- Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for ... science of preclinical discovery into compounds ready for assessment in large clinical populations.We are seeking a highly qualified physician- scientist with a… more
- Merck & Co. (Rahway, NJ)
- …related to oncology compounds.-The Executive Director/PDT lead may:-Manage Directors and/or Senior Directors responsible for Oncology Global Clinical Development ... Job DescriptionOur Clinical Development teams manage studies to provide the...technology and applying rigorous scientific and ethical standards.-The Distinguished Scientist (Executive Director) and Product Development Team (PDT) lead,… more
- Merck & Co. (South San Francisco, CA)
- …Imaging Biomarkers group within Translational Medicine is seeking applicants for a Senior Scientist position, In Vivo Imaging, available at our South ... of disease biology and develop novel biomarkers to inform clinical trial design. -You will be also a part...to bring key molecules from discovery to phase 2 clinical trials. Primary Responsibilities: Discover and development of novel… more
- Merck & Co. (Rahway, NJ)
- …projects under supervision in Late Development Statistics. --Interacts with Clinical , Regulatory, Statistical Programming, Data Management and other company Research ... Laboratories Scientists in designing and analyzing clinical trials, and in coordinating the statistical... trials, and in coordinating the statistical activities for clinical drug/vaccine projects.The incumbent may initially work in a… more
- Merck & Co. (Lower Gwynedd, PA)
- …contribute to optimization and troubleshooting of assays, method validation, and testing clinical samples.The responsibilities of the Scientist will be to work ... developing and expanding your career.We are seeking a highly motivated Scientist to join the Department of Pharmacokinetics, Dynamics, Metabolism, and Bioanalysis… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryThe Principal Scientist /Director, Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which includes ... Outcomes Research, and will support Pneumococcal Vaccines.Under the guidance of a senior leader, this position supports value evidence outcomes research plans and… more
- Merck & Co. (Rahway, NJ)
- …to join Biologics Process Research & Development (BPR&D) as a Principal Scientist .BPR&D within Research Laboratories is on a mission to rapidly deliver diverse ... To achieve this, we work closely with colleagues in Discovery, Pre- clinical , Early Development, Analytical, Formulation, and Commercial Manufacturing while providing… more
- Merck & Co. (Rahway, NJ)
- Job Description BPR&D Downstream Principal Scientist Job Description: - - Our Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, ... bioprocessing to join Biologics Process Research & Development (BPR&D) as a Principal Scientist .- - BPR&D within our company's Research Lab oratories is on a mission… more
- Merck & Co. (North Wales, PA)
- …for the benefit of patients and global human health.Responsibilities: The Senior Statistical Programmer, Submission Data Standards Quality Management (SDS QM), ... for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes submission data standards… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing applications/supplements ... laboratory members, the Contract Manufacturing Organization (CMO), Labeling members and Clinical members. This position works with non-standard problems of some… more
- Merck & Co. (Rahway, NJ)
- …statistical analysis and reporting deliverables under the guidance of a senior -level programmer supporting early-phase oncology clinical trials. Collaborate with ... well as stakeholders in data management, medical writing, and clinical operations to gather and document requirements for statistical...and complete programming tasks under the guidance of a senior programmer at a project level; and to collaborate… more
- Merck & Co. (Rahway, NJ)
- …listings, figures and submission deliverables under the guidance of a senior level programmer.Perform validation tasks according to departmental SOPs and collaborate ... at least 2 years SAS programming experience in a clinical trial environment. Required experience and skills Must possess...and complete programming tasks under the guidance of a senior programmer at a project level; and to collaborate… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage … more
- Merck & Co. (San Diego, CA)
- …(DAGS) department at our company is seeking a highly motivated and skilled data scientist to join our Translational Immunology Analytics team based in San Diego, CA. ... data warehousing concepts, particularly for integrating diverse biological and clinical datasets.Familiarity with drug-target interaction databases and resources relevant… more
- Arrowhead Pharmaceuticals (Verona, WI)
- Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the ... to address diseases outside of the liver, and our clinical pipeline includes disease targets in the liver and...Quality Control structure under the Quality Department. An Associate Scientist I, Quality Control will support the analytical testing… more
- Ionis (Carlsbad, CA)
- …our unique culture while you develop and expand your career! SR. SCIENTIST /ASSISTANT DIRECTOR, ANALYTICAL DEVELOPMENT & QUALITY CONTROL Seeking an experienced ... chemist to join our AD/QC group at the Sr. Scientist or Assistant Director level. The ideal candidate will...and Controls (CMC) and other relevant disciplines such as Clinical and Toxicology Author scientific reports and portions of… more
- Cytokinetics (South San Francisco, CA)
- …for the benefit of patients. We are seeking a highly skilled and motivated Senior Scientist with expertise in small molecule synthesis and process development. ... regulatory guidelines Prepare technical development reports and support authoring of clinical regulatory filings and responses to Health Authority inquiries (eg,… more
- Loyola University Chicago (Chicago, IL)
- …fully grant funded? Yes Duties and Responsibilities The main responsibilities of the Senior Staff Scientist (AbbVie fellow) will include the following: Gain ... Position Details Position Details Job Title SR STAFF SCIENTIST Position Number 8150528 Job Category University Staff Job Type Full-Time FLSA Status Exempt Campus… more
