- Merck & Co. (Boston, MA)
- … Scientist has primary responsibility for protocol development and medical /scientific oversight of clinical research studies involving investigational or ... through interaction with key scientific leaders.Specifically, the Senior Principal Scientist is responsible for:Planning clinical trials (design, operational… more
- Merck & Co. (Rahway, NJ)
- …(GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and has ... Ambition - Respect - Inclusion.Design and organization of paper and Electronic Data Capture (EDC) clinical studies that meet scientific and regulatory… more
- Insmed Incorporated (San Diego, CA)
- … medical monitoring, and query resolution for the protocol and work with other clinical scientist (s), medical monitors, and drug safety to provide support ... in. Are you?About the Role:We're looking for a Director, Clinical Scientist for the Gene Therapy ...scientific input and review of clinical study data , support in assessing medical monitoring reports,… more
- Merck & Co. (North Wales, PA)
- … Clinical Research, Clinical Research Management, Clinical Studies, Clinical Testing, Clinical Trials, Data Analysis, Decision Making, Drug ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide...teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs,… more
- Merck & Co. (Rahway, NJ)
- …and implement analytical methods to support release and stability testing of clinical materials.Perform data entry, data review, and author ... The Small Molecule Analytical Research and Development group has an opening for a Scientist based in Rahway, NJ. Join us and experience our culture first-hand - one… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Scientist , Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management efforts in ... launch and post-market surveillance. Key Responsibilities and Activities: The Senior Scientist , Device System - Device Risk Management will be responsible for… more
- Merck & Co. (Rahway, NJ)
- …Small Molecule Analytical Research and Development group has an opening for a Scientist based in Rahway, NJ. Join us and experience our culture first-hand - ... talented and dedicated colleagues while developing and expanding your career.In your role as Scientist , you will be part of a team of Analytical Chemists working on… more
- Merck & Co. (Rahway, NJ)
- …our company Research Laboratories Division is seeking applicants for a Principal Scientist position available at its Rahway, New Jersey research facility. The ... Principal Scientist is a senior scientific role tasked with working...understanding of Critical Quality Attributes/QbD/DOE principles as well as data analysis and statistics for setting specifications - Ability… more
- Merck & Co. (South San Francisco, CA)
- … development considerations for respiratory medicines.Ability to leverage data analytics and digital tools to support decision-making.#EligibleforERP-Required ... Job DescriptionWe are seeking an experienced scientist to join our team and drive innovation...track record of advancing programs from early discovery through clinical development. This role offers the opportunity to shape… more
- Merck & Co. (South San Francisco, CA)
- …(DPS) group based in South San Francisco, CA is seeking an Principal Scientist with small molecule and peptide experience.DPS is a multi-disciplinary research group ... drug discovery interface. Our team is responsible for the characterization of pre- clinical drug candidates' physicochemical properties. We aim to work with partner… more
- Merck & Co. (North Wales, PA)
- …related drug/vaccine projects in Late Development Statistics.Lead the interaction with Clinical , Regulatory, Statistical Programming, Data Management, and other ... and ascertains needs for potential program development of novel statistical methodology.Analyzes data and interprets results from clinical trials to meet… more
- Merck & Co. (North Wales, PA)
- …project level Position Specific Required Skills and Experience: Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic ... in CDISC SDTM and ADaM standardsSignificant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPHDesigns… more
- Merck & Co. (Rahway, NJ)
- …be programmed, an understanding of statistical terminology and concepts.Familiarity with clinical data management conceptsExperience in CDISC and ADaM ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Eisai, Inc (Exton, PA)
- At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... review and/or author all method transfers related documents.Review laboratory data to support product release, characterization, stability assessment, assay… more
- Merck & Co. (North Wales, PA)
- …be programmed; an understanding of statistical terminology and conceptsFamiliarity with clinical data management conceptsExperience in CDISC and ADaM ... Specific Required Skills and Experience: Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH;… more
- Merck & Co. (North Wales, PA)
- …and information into simple readable form.Solid project management skills.Familiarity with clinical data management concepts.Strategic thinking ability to turn ... deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects.Be accountable for submission data standards… more
- Pfizer (Groton, CT)
- … study results Support execution for all FIH programs through proof-of concept Set the clinical data review strategy, ensure quality data and conduct review ... of emerging clinical data and trends; review and query data ;...paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical… more
- Merck & Co. (Rahway, NJ)
- …ob description This position will be responsible for leading and implementing medical device and combination product design controls for both new products and ... development and design control principles to positively support and influence clinical and commercial combination product development and launches to ensure they… more
- University of Rochester Medical Center (Rochester, NY)
- Head and Neck Oncologic Surgeon Position Highlights Clinical Excellence : Provide the full range of head and neck oncologic care at our Otolaryngology Clinic and ... the forefront of research, community engagement, education, training, and life-saving clinical care Academic Opportunities : Engage in teaching, research, and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and complete study team list is maintained.-In partnership with the lead physician, Clinical Scientist and all study team members, accountable for the ... activities in collaboration with the CRO, feasibility team and the study team.-Assist Data Management with development of the clinical database (edit checks, CCG… more
