- Merck & Co. (North Wales, PA)
- Job DescriptionThe Senior Statistical Programmer, Study Data Tabulation Model (SDTM), provides oversight and creation of the Study Data Tabulation Mode (SDTM) ... predominantly includes creation and validation of Case Report Tabulation (SDTM) study data deliverables Study Data Tabulation Model (SDTM) dataset,… more
- Merck & Co. (Rahway, NJ)
- …following: - Responsible for specific clinical/scientific activities on a single study or across multiple studies (eg, medical monitoring, lab specimen ... more clinical trials. You will assist the Lead Clinical Scientist and study team with the scientific...study team with the scientific conduct of clinical studies . In this position, you will have the opportunity… more
- Merck & Co. (North Wales, PA)
- …dedicated colleagues while developing and expanding your career.-- Director (Principal Scientist ) has primary responsibility for the planning and directing of ... will manage the entire cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.Evaluating… more
- Merck & Co. (North Wales, PA)
- …colleagues while developing and expanding your career.The Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical ... will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically,… more
- Catalent (St. Petersburg, FL)
- Associate Scientist I II , Product Development Position Summary Catalent is a global, high-growth, public company and a leading partner for the pharmaceutical ... to solve difficult development and manufacturing challenges . The Associate Scientist III, Product Development contributes significantly to the successful timely… more
- Merck & Co. (Rahway, NJ)
- …DescriptionJob Description:The Sterile and Specialty Products (SSP) group is responsible for developing non-oral dosage forms (injections, implants, inhaled, ocular) ... for small, intermediate, and large molecules from preclinical toxicology studies to commercialization. Our development teams ensure robust composition, primary… more
- Merck & Co. (Rahway, NJ)
- …analytical characterization and design focused engineer. This position will be responsible for technical interrogation of the various drug delivery device technology ... (DV) strategies and mechanical tests with validations, including engineering studies , design verification protocols, stability studies and validation… more
- Merck & Co. (North Wales, PA)
- …for the benefit of patients and global human health. The incumbent is responsible for statistical planning and data analysis of Phase I/II oncology clinical trials ... well as statistical support for translational oncology projects and studies .-Interact with Clinical, Regulatory, Statistical Programming, Data Management, and other… more
- Merck & Co. (Rahway, NJ)
- …include the following: - May have specific operational responsibilities for a single study or across multiple studies (eg, operational deliverables, clinical & ... ancillary supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities). - May be responsible for tracking study … more
- Sunrise System Inc (Trenton, NJ)
- …purpose is to support programs as they transition from discovery to a FIH study . The qualified candidate will be responsible for running various experiments ... Job Description: Position is 100% onsite. We are seeking a scientist with a strong interest in immunology to join our early translational group in Lawrenceville, NJ.… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …upon team composition and scope of program, the CS lead may also be responsible for study level clinical sciences responsibilities, as well as clinical and ... asset program. This Clinical Science (CS) lead will be responsible for leading and managing one or more clinical...clinical trial protocols, review of clinical data and Clinical Study Reports (CSRs)/outputs throughout the project life cycle. The… more
- Merck & Co. (North Wales, PA)
- …colleagues while developing and expanding your career.The Clinical Director (Principal Scientist ) has primary responsibility for the planning and directing clinical ... will manage the entire cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.-Specifically,… more
- Merck & Co. (North Wales, PA)
- …of the Executive Director, Companion Diagnostics/In Vitro Diagnostics, the Principal Scientist /Director will be responsible for:Providing critical strategic and ... PMAs, 510(k)s, IVDR submissions to NB, IDEs, EU performance study applications, pre-submissions).-Reviewing and authoring relevant sections of diagnostic regulatory… more
- Kelly Services (Raritan, NJ)
- …holiday, vacation, and sick/personal time. **PRINCIPAL RESPONSIBILITIES:** + Partners with Study Responsible Physician SRP to provide clinical oversight to ... Kelly Services is currently seeking a **Senior Clinical Project Scientist ** (Associate Director) for a long-term engagement with one...the study . + Develops clinical research protocols, study … more
- Actalent (Alameda, CA)
- …teams for a specific product candidate, the Clinical Scientist is responsible for designing, preparing, and initiating study protocols and other required ... Job Title: Senior Clinical Scientist Job Description In collaboration with the clinical...area of Oncology. + In collaboration with the clinical study teams for a specific product candidate in clinical… more
- Actalent (New Britain, PA)
- Natural Resources Scientist /Project Manager Job Description The Natural Resources Scientist is responsible for leading all phases of wetlands delineation and ... permitting, threatened and endangered species surveys, state and federal impact studies , and construction monitoring projects. This role includes direct client… more
- Air Force Materiel Command (Eglin AFB, FL)
- …means of accomplishing the mission. Responsibilities Serves as senior level computer scientist , responsible for evaluating computer programs necessary to support ... of this position is to serve as senior computer scientist in the evaluation and implementation of computer programs...improve overall mission effectiveness. To manage the conduct of studies to determine the most efficient and cost effective… more
- J&J Family of Companies (Skillman, NJ)
- …NJ in or around early 2025._ **Travel %:** 10% **What you will do** The Senior Scientist is responsible for serving as a member of the Skin Health Clinical ... Sr Scientist SH Claims Clinical - 2407021764W **Description** Kenvue...studies for new products. + Serve as the Study Director and fulfill the responsibilities for this role… more
- Pfizer (Pearl River, NY)
- …day, is in line with an unwavering commitment to quality. The Associate Scientist is responsible for providing laboratory equipment support for the execution ... the world. **What You Will Achieve** As an Associate Scientist , you will be at the center of our...preclinical and clinical serology studies to support vaccine development & clinical studies… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …excellence of our academic community. **Description** JOB DESCRIPTION: + The Research Data Scientist is responsible for mining and analyzing data from various ... problems and/or answer research questions. + The Research Data Scientist is adept at using large data sets and...imaging, device, -omics) from both clinical care and research studies . + This person will collaborate with Researchers throughout… more
