- Merck & Co. (North Wales, PA)
- …Clinical Trial Team lead. Leads and directs teams in key study planning, development, and execution elements (eg operational reviews, issue escalation/mitigations, ... Responsible for facilitating and collaborating with key internal/external stakeholders ( study team, subsidiary country teams, vendors, committees, etc.) in support… more
- Merck & Co. (North Wales, PA)
- …serve as the clinical trial team leadMay lead team in key study planning, development, and execution elements (eg, data management deliverables, trial level ... investigator-meeting planning, communication plans, preparation of status update reports, study close out activities).Leads team for timeline management, risk… 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, ... 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
- Merck & Co. (Rahway, NJ)
- …and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case ... payers, policymakers, HTA/reimbursement agencies, and health systems globally.Types of studies executed include prospective and retrospective observational studies… more
- Merck & Co. (Boston, MA)
- …to the following: conduct TK modeling to support dose-selection on toxicity studies , provide TK study design, calculate PK/TK parameters, interpret results, ... quality scientific results according to agreed timeline for several concurrent studies .Effectively communicate study results at internal meetings, as… more
- Merck & Co. (North Wales, PA)
- …Driving License:Hazardous Material(s):Required Skills:Clinical Affairs, Clinical Studies , Clinical Trials, Medical Affairs, Medical Relations, ... to scientific questions from SLs, including questions about Company products. The work of an RMSD is aligned to: Scientific Exchange, Research, Scientific Congress… more
- Merck & Co. (Rahway, NJ)
- …will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, ... the Director may be responsible for:Evaluating pre-clinical and translational work for the purpose of generating early clinical development plan and Investigational… 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
- Merck & Co. (North Wales, 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. (North Wales, PA)
- …Evidence (RWE) in Oncology.- -Position objectivesTo design and execute real-world evidence studies , designed to demonstrate the value of new products in support of ... inform and contribute to the value evidence plan and associated studies which demonstrate clinical, economic, and patient-centered value. The work… more
- Merck & Co. (Chicago, IL)
- …to scientific questions from SLs, including questions about Company products. The work is aligned to Scientific Exchange, Research, Scientific Congress Support, and ... for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies and serve as a role model for other field medical… more
- Eisai, Inc (Nutley, NJ)
- …As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, ... execution within a pharmaceutical or biotechnology company. This role ensures studies are conducted efficiently, within budget, and in compliance with regulatory… more
- Merck & Co. (North Wales, PA)
- …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
- 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… more
- Eisai, Inc (Nutley, NJ)
- …As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, ... as well as the clinical execution and oversight of the associated studies being conducted globally. The Executive Director will champion transformational business… more
- Merck & Co. (North Wales, PA)
- …include:Collaborating cross-functionally in the development of Protocol and related study materials (eg, ICF documents / amendments); Partners with the ... Study Manager on study deliverables.Ensuring CRF design...California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in office-based… more
- Eisai, Inc (Nutley, NJ)
- …Proficient in MS outlook, word, power point and excelBasic understanding of study related documentationseTMF (Veeva) experience preferredAbility to work with ... As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile,… more
- Merck & Co. (Rahway, NJ)
- …responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e . g . , ICF documents/ amendments); Partners ... with the Study Manager on study deliverables. Ensuring CRF...California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in office-based… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …laboratory at The Mind Research Network. The Research Assistant will work on studies examining various neurocognitive conditions, utilizing neuroimaging ... neurocognitive assessment methods. Responsibilities include, but are not limited to: 1) study participant recruitment, scheduling, and follow-ups 2) study data… more
