- 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
- 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. (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. (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
- Merck & Co. (North Wales, PA)
- …may: Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts in ... safety and efficacy as well as new drug applications, clinical study reports, or publication;Participation in internal...Judgment, Clinical Medicine, Clinical Research, Clinical Research Management, Clinical Studies ,… 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. (Boston, MA)
- …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
- 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
- Insmed Incorporated (NJ)
- …including monitoring of clinical studies , reviewing & interpreting clinical trial data, authoring clinical study and regulatory communications ... for all issues identified which may affect the quality and integrity of clinical studies .Perform medical monitoring, coding, and data cleaning, and prepare… more
- Insmed Incorporated (NJ)
- …to future scenarios within the fieldAssist supply chain colleagues in the clinical study startup processes such as demand forecasting, regulatory submissions, ... than supply chain to achieve FPI (First Patient In) milestones and successful clinical study startAssist in digital solutions to optimize scenario planning and… more
- Merck & Co. (South San Francisco, CA)
- …of Phase I studies ; close collaboration with internal and external clinical study support staff and scientists (including discovery research, biostatistics, ... insight into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human… more
- Merck & Co. (NM)
- …researchIdentifies barriers to patient enrollment and retention efforts to achieve study milestonesUpon request from Global Clinical Trial Operations ... 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. (North Wales, PA)
- …assigned to a development project as neededLead biostatistics in early or late clinical development planning to ensure that study designs are consistent with ... program development of novel statistical methodology.Analyzes data and interprets results from clinical trials to meet objectives of the study protocol.-… more
- Merck & Co. (Salt Lake City, UT)
- …relevant therapeutic area space is highly desirable (ie, experience in late stage clinical research as an investigator or key study personnel conducting outcomes ... investigators who have potential interest in participating in our Company research studies . This role requires you to provide support for data generation activities… more
- Novo Nordisk Inc. (Charlotte, NC)
- … to ensure timely review, initiation, and completion, as well as publication of study results. Provides clinical support in cooperation with other Novo Nordisk ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...and development activities in the medical community Collaborates with trial/ study investigation sites; ensuring effective coordination and facilitation of… more
- Merck & Co. (Rahway, NJ)
- …optimal market/patient access and reimbursement. The incumbent is expected to work cross-functionally with clinical development, medical affairs, biostatistics, ... therapeutic area and encourages appropriate application of new methods to HEOR studies .Maintains responsibility to ensure study conduct is aligned with company… more
- Merck & Co. (South San Francisco, CA)
- …of pre- clinical drug candidates' physicochemical properties. We aim to work with partner groups to select candidates with optimal development properties while ... covers identification of preclinical formulations for pharmacology and toxicology studies and ideally for FIH across a variety of...sets and convey their meaning to the teams you work on and develop strategies to optimize molecules and… more
- Community Medical Center (Point Pleasant, NJ)
- …and other related matters Collaborates with PI & other Team members & Clinical Research Coordinator to ensure that key federal /state/ local regulatory ... Job Title: Clinical Research Nurse Location: CMC Nursing Department Name:...annual salary range for this position if hired to work in New Jersey. The compensation offered to the… more
- Insmed Incorporated (NJ)
- …to the Head of Programming, you'll provide programming and analytical support to clinical studies . You will be working interactively with functional colleagues ... You'll Do: In this role, you'll be responsible for:Provide programming support to clinical studies and submissionsCreation of CDISC compliant SDTM and ADaM… more
- Insmed Incorporated (San Diego, CA)
- …gene delivery and expression in tissue samples from both preclinical models and clinical studies .The successful candidate will work at the interface ... Receive, accession, and verify tissue specimens from preclinical and/or clinical studies .Perform tissue fixation, processing, embedding, and sectioning… more
