- Merck & Co. (Rahway, NJ)
- …function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and ... responsible for the conduct of Good Clinical Practice (GCP) studies , and occasionally Good Laboratory Practice (GLP) studies.... The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a… more
- Insmed Incorporated (NJ)
- …magazine's No. 1 Top Employer for four consecutive years, certification as a Great Place to Work ® in the US, and a place on The Sunday Times Best Places to Work ... limited to, development of project documentation, training project staff, monitoring study progress, assessing protocol adherence, administration and oversight of … more
- Merck & Co. (South San Francisco, CA)
- … studies ; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, drug ... into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human disease in… more
- Insmed Incorporated (NJ)
- …magazine's No. 1 Top Employer for four consecutive years, certification as a Great Place to Work ® in the US, and a place on The Sunday Times Best Places to Work ... effective and efficient execution of all operational aspects of clinical study planning, implementation, data delivery and reporting. Represents Clinical Operations… more
- Merck & Co. (Boston, MA)
- …I studies ; close collaboration with internal and external clinical study support staff and scientistsProvide clinical pharmacology support for programs through ... therapies.Our main collaboration is with teams in Boston, MA, but remote work is an option.Translational Medicine is specifically responsible for:Contributing to the… more
- Merck & Co. (Boston, MA)
- …will manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring, ... of external opportunitiesThe Senior Director May: Supervise the execution of clinical studies . Work closely with a cross-functional group of experts in… more
- Merck & Co. (North Wales, PA)
- …Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts in commercialization, ... Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new… more
- Merck & Co. (Upper Gwynedd, PA)
- …and programs.In collaboration with internal teams and external partners, designs studies ; authors study protocols; and develops measurement questionnaires, case ... technology assessment (HTA)/reimbursement agencies and health systems globally.Types of studies executed include prospective and retrospective observational studies… more
- Merck & Co. (Upper Gwynedd, PA)
- …may: Supervise the activities of Clinical Scientists in the execution of clinical studies . -- Work closely with a cross-functional group of experts in ... Director will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. --… more
- Merck & Co. (MA)
- …Director may:Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts in ... determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and… more
- Merck & Co. (North Wales, PA)
- …with the Investigator Study Program Committee to evaluate outcomes research study protocols for studies in local markets.Supports affiliates to understand ... and gain input on research design and implementation of retrospective database studies , assessment of patient reported outcomes, epidemiological studies and… more
- Insmed Incorporated (San Diego, CA)
- …delivery and expression in tissue samples from both preclinical models and clinical studies .The successful candidate will work at the interface of research and ... magazine's No. 1 Top Employer for four consecutive years, certification as a Great Place to Work ® in the US, and a place on The Sunday Times Best Places to Work… more
- Merck & Co. (Rahway, NJ)
- …plans for all activities associated with clinical supplies for their assigned studies , which could vary in complexity. This individual serves as the primary ... Responsible and accountable for establishing the timelines for clinical-supply-needs-per study and providing-the signal for sourcing, manufacturing, packaging, and… more
- Merck & Co. (Rahway, NJ)
- …Is involved in late clinical development planning (LDP) to ensure that study designs are consistent with program objectives and meet worldwide regulatory and ... data and interprets results from experiments to meet objectives of the study protocol.- Independently applies and implements basic and complex techniques to these… more
- Insmed Incorporated (NJ)
- …magazine's No. 1 Top Employer for four consecutive years, certification as a Great Place to Work ® in the US, and a place on The Sunday Times Best Places to Work ... collaborate across functions to support downstream analyses from in vivo studies .What You'll Do: Lead cell-based assay development, perform efficacy assessment… more
- Insmed Incorporated (NJ)
- …degree or higher in Statistics, Computer Science, Mathematics, Engineering or related field of study is a plus.Minimum 5-7 years of work experience in a ... four consecutive years, certification as a Great Place to Work ® in the US, and a place on The...Programming will provide statistical programming and analytic support clinical studies . As a team member of the Programming function,… more
- Cipla (Hauppauge, NY)
- …of supporting and participating in compliance and regulatory audits at the local and federal levels. Ability to work in a fast-paced, dynamic environment within ... or Affiliates. Job Title : QA Validation FLSA Classification : Professional, Exempt Work Location : Unit 1, Hauppauge, NY Work Hours: General: 8:30AM… more
- Insmed Incorporated (San Diego, CA)
- …magazine's No. 1 Top Employer for four consecutive years, certification as a Great Place to Work ® in the US, and a place on The Sunday Times Best Places to Work ... and in vivo samples. Additionally, the scientist will document his/her methods and studies and participate in the technical transfer of assays to third party… more
- Merck & Co. (North Wales, PA)
- …and simulation stakeholders spanning both early and late-stage Oncology studies . Accountability predominantly includes the development and execution of statistical ... validate and maintain modeling datasets, tables, listings and figures at study / protocol levelAssure deliverables quality and compliance with departmental SOPs… more
- BioAgilytix (San Diego, CA)
- …we are growing. Our culture is fast-paced, fun and never boring. Because we work across numerous clients and drug modalities, your career can develop rapidly. You'll ... activities in support of preclinical, clinical, and product release studies for our San Diego lab. This role requires...being the expert in using tools/software relevant to the team. Work closely with clients to assure successful on time… more
