- Merck & Co. (San Diego, CA)
- …(eg, study team, country teams, vendors, committees) in support of clinical study objectives.-Accountable for managing any study specific partners ... - DayValid Driving License:YesHazardous Material(s):NoRequired Skills:Adaptability, Clinical Data, Clinical Operations, Clinical Study Design, … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to ensure the effective and efficient execution of operational aspects of clinical study planning, implementation, data delivery and reporting. Will represent ... relevant to the Clinical Operations function. Will ensure that global and local clinical studies are executed, in adherence to Good Clinical Practices… more
- Merck & Co. (Upper Gwynedd, PA)
- …support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and participating in internal and joint ... The Senior Director will manage the entire cycle of clinical development, including study design, placement, monitoring,...of Clinical Scientists in the execution of clinical studies . --Work closely with a cross-functional… more
- Merck & Co. (Boston, MA)
- …manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring, ... safety and efficacy as well as new drug applications, clinical study reports, or publicationParticipation in internal...of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional… more
- Merck & Co. (Rahway, NJ)
- …decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication;Participation in internal and joint ... Supervise the activities of Clinical Scientists in the execution of clinical studies .Work closely with a cross-functional group of experts in… more
- Merck & Co. (Rahway, NJ)
- …support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in internal and joint ... may:Supervise the activities of Clinical Scientists in the execution of clinical studies .Work closely with a cross-functional group of experts in… more
- Merck & Co. (Rahway, NJ)
- …decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publicationParticipating in internal and joint ... the Senior Director will manage the entire cycle of clinical development, including study design, initiation, execution,...Development, Clinical Medicine, Clinical Research, Clinical Research Management, Clinical Studies ,… more
- Merck & Co. (Rahway, NJ)
- …Arrangements:RemoteShift:1st - DayValid Driving License:NoHazardous Material(s):NoRequired Skills:Adaptability, Clinical Quality Management, Clinical Study ... research division QA and acting as the link between Clinical Development, study teams, global business functions...of the quality management system are in place for studies conducted in partnership with non-commercial organizations (eg NGO,… more
- Merck & Co. (Rahway, NJ)
- …- DayValid Driving License:YesHazardous Material(s):NoRequired Skills:Adaptability, Clinical Data, Clinical Operations, Clinical Study Design, ... macular degeneration), thyroid eye disease.Experience in developing protocols and study related documents for ophthalmology clinical trials.Experience with… more
- Eisai, Inc (Nutley, NJ)
- …external partnerships to equip and adapt the workforce to evolving technologies.Align clinical portfolio, business strategy, clinical studies , and related ... If this is your profile, we want to hear from you. The Clinical Quality Assurance Professional (QAP) position is responsible for design, delivery and execution… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Summary: This position is responsible for enabling the on-time delivery of clinical supplies across the DSI portfolio. This role is primarily responsible for ... supporting CSO Project Management Leads by developing and updating Study Supply Plans, managing various work streams with key service providers and working with… more
- Merck & Co. (North Wales, PA)
- …and medical monitoring of clinical studies .Supervises development of clinical documents including protocols, clinical study reports and background ... Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle… more
- Merck & Co. (Rahway, NJ)
- …or Manufacturing O rganizations . - Facilitate manufacturing, packaging , and release of clinical supplies for clinical studies , assist in scale up ... Job DescriptionOur company's Pharmaceutical Sciences and Clinical Supply organization translates molecules to medicines, working from the discovery interface through… more
- Eisai, Inc (Nutley, NJ)
- …Functions Independently conduct audits Review and oversee results of CQA audits of study sites, clinical vendors, clinical documents, and internal process ... audits Facilitate Sponsor health authority inspections of global clinical facilities and study sites Continuously drive innovation through active search,… more
- Merck & Co. (Sacramento, CA)
- …from investigators and provides information regarding participation in Company-sponsored clinical studies Scientific Congress Support Engages in scientific ... researchIdentifies barriers to patient enrollment and retention efforts to achieve study milestonesUpon request from Global Clinical Trial Operations… more
- Merck & Co. (Cincinnati, OH)
- …and publication in Virology is highly desirable (ie, experience in late stage clinical research as an investigator or key study personnel conducting outcomes ... Work Arrangements:RemoteShift:Not IndicatedValid Driving License:YesHazardous Material(s):n/aRequired Skills:Advisory Board Development, Clinical Testing, HIV AIDS, Investigator-Initiated Studies (IIS),… more
- Merck & Co. (Rahway, NJ)
- …support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipating in internal and joint ... The Senior Director will manage the entire cycle of clinical development, including: study design, placement, monitoring,... Clinical Research, Clinical Research Management, Clinical Risk Management, Clinical Studies ,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …direction for respective interventional/non-interventional programs such as post marketing studies or post approval commitments, medical access programs.Partner with ... execution of Interventional, Non-Interventional, Managed Access Programs, and Investigator-Initiated Studies .Provide comprehensive quality oversight for Medical Affairs activities, including… more
- Merck & Co. (Rahway, NJ)
- …company-sponsored studies and areas of interest for the investigator-initiated study program (MISP) The Sr. GDMA chairs the Global Medical Affairs Teams ... that address asset value proposition, insights from affiliates and regions, and clinical and value evidence gaps. Translate these Goals and Strategies into research,… more
- Merck & Co. (North Wales, PA)
- …real-world evidence data generation and coordinates local data generation studies with V&I Outcomes ResearchSupports the Investigator-Initiated Study ... Development Team, Global Brand and V&I Outcomes Research leads to define clinical development plans and brand strategies for assigned TAsProvides a solid… more
