- Merck & Co. (Rahway, NJ)
- …Laboratory Practice (GLP) studies . The Associate Principal Scientist is the primary clinical study team leader and has overall responsibility for a study ... Respect - Inclusion.Design and organization of paper and Electronic Data Capture (EDC) clinical studies that meet scientific and regulatory requirements by the… more
- Merck & Co. (Rahway, NJ)
- …assessments of external opportunitiesThe Senior Director May: Supervise the execution of clinical studies . Work closely with a cross-functional group ... manage the entire cycle of late-stage clinical development and studies , including development strategy, study design, initiation, execution, monitoring,… 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 ... safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in...Skills: Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies ,… more
- Merck & Co. (Rahway, NJ)
- …(Protocol CSPM) designs strategic and operational plans for all activities associated with clinical supplies for their assigned studies , which could vary in ... topics. Responsible and accountable for establishing the timelines for clinical -supply-needs-per study and providing-the signal for sourcing, manufacturing,… more
- Merck & Co. (Rahway, NJ)
- …Director may:Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts ... The Clinical Director May Be Responsible For:Evaluating pre- clinical and translational work for the purpose...safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in… more
- Merck & Co. (Boston, MA)
- …decisions regarding safety and efficacy as well as new drug applications, clinical study reports, and publicationsParticipating in internal and joint ... and drug development (at least 5 years)Demonstrated success in overseeing clinical studies and protocolsDemonstrated record of scientific scholarship and… more
- Insmed Incorporated (NJ)
- …to ensure the effective and efficient execution of all operational aspects of clinical study planning, implementation, data delivery and reporting. Represents ... vendor management, GCP, etc.Develops operational strategies for implementation of clinical studies regionally/globally in conjunction with project teams… more
- Merck & Co. (North Wales, PA)
- …partnership with our research division QA and acting as the link between Clinical Development, study teams, global business functions and regional study ... Job DescriptionIn partnership with the Clinical Quality Operations Lead (CQOL and Head of...inspection observations as appropriate.- In addition, the CQOM will work with peers to analyze data across therapy areas… more
- Insmed Incorporated (San Diego, CA)
- …(SOPs).What You'll Do: Participate in cross functional teams to develop and implement clinical studies within clinical program(s). Collaborate with internal ... patients with serious diseases. Reporting to the Executive Director, Clinical Development, you will support and work ...(CROs), and external vendors to prepare, review and finalize clinical study documents and plans Contribute to… more
- Merck & Co. (Rahway, NJ)
- …in ophthalmology clinical trials.Required Skills: Adaptability, Clinical Data, Clinical Operations, Clinical Study Design, Clinical Trial ... macular degeneration), thyroid eye disease.Experience in developing protocols and study related documents for ophthalmology clinical trials.Experience with… more
