- 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)
- …Engineering or related field plus 3 years SAS programming experience in a clinical trial environment OR a Bachelor's degree in Computer Science, Statistics, Applied ... or related field plus 5 years SAS programming experience in a clinical trial environment.Minimum requirement:Must have experience in CDISC SDTM and ADaM… 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 DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist /Associate Director, has primary responsibility for ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… 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. (North Wales, PA)
- …resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, ... reimbursement. The incumbent is expected to work cross-functionally with clinical development, medical affairs, biostatistics, market access, commercial and country… 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. (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. (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 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. (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
- Soliant (Santa Ana, CA)
- Minimum 1+ years Medical Tech experience required.Travel Clinical Lab Scientist Night Shift Near Santa Ana, CA Contract Length: 13 Weeks Schedule:Evenings,10:00 ... Just 30 minutes from Laguna Beach We're hiring a Clinical Lab Scientist (CLS) for a night...Apply today to get started! Contact Information: Ivory Smith Senior Account Executive -Lab Staffing Specialist Soliant Health ###… more
- Monster (Cambridge, MA)
- Job Title: Scientist II | Senior Scientist Location: Cambridge, MA Duration : 6+ Months Shift: Standard Payrate: $50- $55/ hr. on W2 Job Description: . We ... are looking for a talented individual to fill an eight-month Scientist II/ Senior Scientist contract position in . Protein Sciences (Purification and… 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
