- 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 ... include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary function...Respect - Inclusion.Design and organization of paper and Electronic Data Capture (EDC) clinical studies that meet… more
- Merck & Co. (Boston, MA)
- …through interaction with key scientific leaders.Specifically, the Senior Principal Scientist is responsible for:Planning clinical trials (design, operational ... Clinical Judgment, Clinical Medicine, Clinical Research Management, Clinical Trial Development, Clinical Trials, Data Analysis, Drug Development,… 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)
- …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
- Insmed Incorporated (San Diego, CA)
- …the future of science, we're in. Are you?About the Role:We're looking for a Director, Clinical Scientist for the Gene Therapy Clinical Development team to ... reporting of results Provide scientific input and review of clinical study data , support in assessing medical...query resolution for the protocol and work with other clinical scientist (s), medical monitors, and drug safety… 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
- Twist BioScience (South San Francisco, CA)
- Scientist / Sr Scientist / Staff Scientist (NGS Applications) in South San FranciscoJob DescriptionWe are seeking a highly motivated and technically ... proficient Scientist to join our dynamic Next-Generation Sequencing (NGS) product...in molecular biology and NGS workflows to generate high-quality data , provide critical technical insights, and drive scientific communication… 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)
- …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. (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. (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
- 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
- Aequor (Thousand Oaks, CA)
- …Oaks Global Critical Reagents (GCR) Team is looking for an experienced, hands-on scientist to join the GCR - Process Excellence (GCR-PEX) team. This senior role ... This engagement requires conformance with site policies, safety, quality, and data -integrity requirements. The successful candidate must model 's mission and the… more
- Merck & Co. (Rahway, NJ)
- …development and design control principles to positively support and influence clinical and commercial combination product development and launches to ensure they ... Regulatory teams to ensure compliance with applicable global regulations. Leverage data analytics and key performance indicators to monitor process performance.… more
- Insmed Incorporated (NJ)
- …for the future of science, we're in. Are you?About the Role:The Associate Scientist will work with a multidisciplinary team of research scientists to investigate ... therapeutics for treating neutrophil-mediated diseases across several pre- clinical projects. This will involve assisting with tasks such as cell culture, in vitro… 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
- Eisai, Inc (Exton, PA)
- …review and/or author all method transfers related documents.Review laboratory data to support product release, characterization, stability assessment, assay ... of recombinant proteins.Demonstrated knowledge of biopharmaceutical development through all clinical phases and post-commercialization.Strong familiarity with cGMP/ICH/FDA/EMA regulations and… more
- Parexel (Trenton, NJ)
- …(SOM) + When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist ) + May act as a Mentor for ... regulatory requirements + Demonstrated understanding of key operational elements of clinical research (eg, monitoring, data acquisition and cleaning, reporting,… more
- NORC (Chicago, IL)
- …prescribing practice requirements, and interpretations of comparative effectiveness of outcomes based on clinical trial data + Utilize data and literature to ... to pharmaceutical drug prescribing practices + Develop protocols for and conduct clinical trial literature reviews and data extraction. + Conduct systematic… more
