- Merck & Co. (North Wales, PA)
- …field experienceDegree in life sciences, preferred.Experience in planning and executing clinical studies in ophthalmology highly preferredAs an Equal Employment ... the operational planning and execution of one or more clinical trials. In this position, you will have the...Trial Team lead. Leads and directs teams in key study planning, development, and execution elements (eg operational reviews,… more
- Merck & Co. (North Wales, PA)
- …(eg, study team, country teams, vendors, committees) in support of clinical study objectives.Accountable for managing any study specific partners ... Skills:Adaptability, Adaptability, Clinical Data, Clinical Operations, Clinical Research, Clinical Study Design, Clinical Testing, Clinical… more
- Merck & Co. (Rahway, NJ)
- …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)
- …support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in internal and joint ... Clinical Scientists in endeavors ranging from drafting clinical study protocols to overseeing protocol adherence...appropriate corporate personnel are informed of the progress of studies of our companies and competitors' drugs and internal… more
- Merck & Co. (North Wales, PA)
- …Adaptability, Clinical Data, Clinical Operations, Clinical Outcomes, Clinical Research, Clinical Study Design, Clinical Testing, ... SummaryThis position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof.- In this position, you will have the… more
- Merck & Co. (Rahway, NJ)
- …supply related topics . - Responsible and accountable for establishing the timelines for clinical supply needs per study and providing the signal for sourcing, ... to establish a consolidated , visible forecast for all study product needs (Bulk Drug Product and Clinical...d evelopment and User Acceptance Testing (UAT) for assigned studies . - Mentors new team members and supports… more
- Merck & Co. (Rahway, NJ)
- …Sciences, Clinical Data, Clinical Data Interpretation, Clinical Operations, Clinical Research, Clinical Study Design, Clinical Testing, ... scientific -pl anning and execution of one or more clinical trials or significant aspects thereof . In this...Collaborating cross-functionally in the development of Protocol and related study materials (e . g . , ICF documents/… more
- Eisai, Inc (Nutley, NJ)
- … Lead or Clinical Program Director accountability. Proven experience in running clinical studies with an understanding of Clinical Operations and Data ... clinical development plans of the respective compounds as well as the clinical execution and oversight of the associated studies being conducted globally.… more
- Eisai, Inc (Nutley, NJ)
- …These activities directly impact the timeliness, quality, and successful execution of clinical studies in accordance with the overarching project plans ... operations activities.Ensure the timely, quality, and successful execution of clinical studies in alignment with project plans...Clinical Operations staff to oversee all aspects of clinical trial development.Lead clinical study … more
- Merck & Co. (Rahway, NJ)
- …CSPM) creates strategic and operational plans associated with the downstream activities of clinical supplies for their assigned studies . -The primary function of ... utilizing key technological tools in the planning and managing of clinical supplies for assigned studies such as IRT & Microsoft PowerApps. -Works directly in… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... Company's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...ensures proper allocation of drug product as needed across studies within assigned program(s) . - Responsible for identifying… more
- Eisai, Inc (Nutley, NJ)
- …you. The Clinical Trial Assistant will support all phases of clinical study activities (feasibility, start-up, conduct and close-out) under the direction ... and supervision by study Clinical Operations Lead(s). Plans, support, creates, and communicates clinical study timelines. Gathers input from… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …biomarker strategy in collaboration with Translational Medicine/Clin Pharm; May act as Clinical study leader (CSL) Study Planning and Execution: Provides ... medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams.Responsibilities: Study Strategy: Provides the… more
- Eisai, Inc (Nutley, NJ)
- …Environment Implementation of new programs, enhancements & support of Eisai Clinical Computing Environment Support study migration, program validation, technical ... is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges in the programming… more
- Merck & Co. (North Wales, PA)
- …Travel Requirements: Flexible Work Arrangements:RemoteShift:Valid Driving License:Hazardous Material(s):Required Skills: Clinical Affairs, Clinical Studies , ... researchIdentifies barriers to patient enrollment and retention efforts to achieve study milestonesUpon request from Global Clinical Trial Operations… 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. (North Wales, PA)
- …and programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case ... lead cross-functional teams is a critical part of this role.Types of studies executed include prospective and retrospective observational studies to characterize… more
- Merck & Co. (Chicago, IL)
- …from investigators and provides information regarding participation in Company-sponsored clinical studies . Scientific Congress Support Engages in scientific ... - DayValid Driving License:YesHazardous Material(s):n/aRequired Skills: Clinical Immunology, Clinical IT, Clinical Studies , Clinical… 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
