- 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 ... Quality Assurance audit reviewGenerate project support documentationPerform end of study administrative activitiesAdhere to safety and compliance requirementsAssist in… more
- 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
- Merck & Co. (Rahway, NJ)
- …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. (Boston, MA)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... are developed to produce safe, effective, and innovative medicines, and we work with cross-functional colleagues in Global Medical and Scientific Affairs and Global… 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. (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 five 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
- Pfizer (Groton, CT)
- …proof of mechanism (POM), early signs of efficacy (ESOE) and proof of concept (POC) studies in Oncology. You will work in close collaboration with the Global ... with Pfizer development operations and the project team, to meet enrollment and study delivery timelines. You will also work with other functional disciples… 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 five consecutive years, certification as a Great Place to Work ® in the US, and a place on The Sunday Times Best Places to Work ... to the Executive Director, Clinical Development, you will support and work predominately with the Clinical Trial/Indication Lead(s) and Medical Monitor(s) for… 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
- MCKESSON (Dallas, TX)
- …diagnosed with cancer every day. Our Mission People who live with cancer - those who work to prevent it, fight it, and survive it - are at the heart of every ... your primary responsibility is to screen, enroll and follow oncology research study subjects ensuring protocol compliance and clo se monitoring while patients are… more
- Merck & Co. (CT)
- …investigators who have potential interest in participating in our Company research studies . This role requires you to provide support for data generation activities ... including our Company sponsored trials and our Company Independent Investigator Study Programs as prioritized and requested by our Research Development Division… more
- Merck & Co. (North Wales, PA)
- …to scientific questions from SLs, including questions about Company products. The work of an RMSD is aligned to: Scientific Exchange, Research, Scientific Congress ... for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The RMSD serves as a role model for other field… more
- Merck & Co. (Rahway, NJ)
- …internal teams and external partners, design non-interventional and data synthesis studies , author study protocols, develop measurement questionnaires, case ... report forms, data analysis plans, final study reports, scientific presentations, and publications.Responsible for study -related contracting, budgets, and… more
- Merck & Co. (St. Louis, MO)
- …who have potential interest in participating in our Company's research studies . -Virology RMSDs provide support for data generation activities including our ... Company's sponsored trials and our Company's Independent Investigator Study Programs as prioritized and requested by Research and Development (R&D) leadership.… more
- Merck & Co. (North Wales, PA)
- …Research Organization (CRO) and external statistical consultants.The incumbent may initially work in a specific disease area. Primary activities :Serves as ... biostatistics in early or late clinical development planning to ensure that study designs are consistent with program objectives and meet worldwide regulatory and… 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 ... and oversight of assigned clinical programs including monitoring of clinical studies , reviewing & interpreting clinical trial data, authoring clinical study… 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
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