- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders.Summary Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the ... Participate in training; make recommendations for areas of improvement and innovation ( study , or departmental level). Work with supervisor to provide input… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diseases and immune disorders. Summary This position works with the Director, Clinical Study Startup to establish the strategy driving global Clinical Study ... electronic data capture (EDC) Safety report outputs, reviews clinical study and post-marketing protocols and the Clinical Study...strong organization and interpersonal skills and is able to work effectively with people at different levels of an… more
- Aequor (South San Francisco, CA)
- …trial data insights and to offer data science-related consultation to the study teams. We leverage cutting-edge data science and operation data management to ... facilitate the study start-up planning. We develop advanced analytical data visualization...and best practices. Lead centralized systematic data surveillance across studies in ECD, document surveillance activities, and assess control… more
- Merck & Co. (Rahway, NJ)
- …Trials to enhance the understanding of the scientific foundations and goals of the study , support patient enrollment and retention efforts for a given study or ... to enhance the understanding of scientific foundations and goals of the study , support patient enrollment and retention efforts or address investigator questions.May… more
- Merck & Co. (North Wales, PA)
- …to scientific questions from SLs, including questions about Company products. The work of an Regional Medical Scientific Director is aligned to: Scientific Exchange, ... approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The Regional Medical Scientific Director serves as a… more
- Insmed Incorporated (San Diego, CA)
- …the world who are willing to challenge the status quo, solve problems, and work collaboratively with a sense of urgency and compassion. Guided by our core values ... respect, and integrity, we aim to foster an inclusive, diverse, and flexible work environment, where our employees are recognized for leaning in and rolling up… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …to join our in vivo pharmacology team responsible for conducting in vivo studies with mice and NHP to support pipeline development. This position will report ... extensive knowledge and hands-on experience in conducting in vivo Pharmacology studies , especially in conducting cell-therapy based studies . The candidate… more
- Merck & Co. (Rahway, NJ)
- …Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts in commercialization, ... will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically,… more
- Merck & Co. (Rahway, NJ)
- …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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and external KOLs for protocol development; provides input on CRO and ARO Scope of Work and budget; participates in study team meetings with CRO and ARO; ... of CSL and/or Medical Monitor. Represents Clinical Development on Study Team and collaborates as team member with other...along with CSL and/or Medical Monitor to development of study design to meet study objectives, development… more
- Insmed Incorporated (San Diego, CA)
- …the world who are willing to challenge the status quo, solve problems, and work collaboratively with a sense of urgency and compassion. Guided by our core values ... respect, and integrity, we aim to foster an inclusive, diverse, and flexible work environment, where our employees are recognized for leaning in and rolling up… 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)
- …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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …supporting planning and execution of observational research / Real World Evidence studies to support the Evidence and Insights Generation Plans (EIGPs) for specific ... but not limited to cross-functional team meetings, project team meetings and observational study protocol reviews. One of the key responsibilities for the fellow is… more
- Aequor (Thousand Oaks, CA)
- …with the colleagues in the automation team to coordinate, organize and execute studies Participate in team meetings by sharing study designs, results, and ... bispecific T-cell engagers (BiTEs), fusion proteins, etc.). The Senior Associate will work in a highly collaborative team focusing on high throughput and automation… more
- Merck & Co. (Rahway, NJ)
- …and accountable for establishing the timelines for clinical supply needs per study and providing the signal for sourcing, manufacturing, packaging, and distribution- ... to establish a consolidated , visible forecast for all study product needs (Bulk Drug Product and Clinical Finished...d evelopment and User Acceptance Testing (UAT) for assigned studies . Mentors new team members and supports staff… more
- Insmed Incorporated (San Diego, CA)
- …the world who are willing to challenge the status quo, solve problems, and work collaboratively with a sense of urgency and compassion. Guided by our core values ... respect, and integrity, we aim to foster an inclusive, diverse, and flexible work environment, where our employees are recognized for leaning in and rolling up… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …for and/or participating in Novo Nordisk clinical trials. This role will work cross functionally within Clinical Medical and Regulatory (CMR) to build relationships ... for the sites Collaborate with local teams to actively pursue resolution to study level challenges Develop and maintain a working knowledge and materials of site… more
- Merck & Co. (North Wales, PA)
- …outcomes research activities linked to V&I goals. Responsible for study -related contracting, budgets, and vendor/partner management.Support market affiliates to ... dossiers, and adapt health economic evaluations, according to local requirements. Work closely with cross functional teams to effectively communicate outcomes… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …coordinates complex laboratory duties. The Laboratory Supervisor will organize and coordinate studies in addition to documenting laboratory work and maintaining ... limited scope client interaction to assist management or director study with execution or resolution of study ...continuing scientist reports in their area of expertise. The work is performed in a highly regulated environment and… more
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