- Novo Nordisk Inc. (Stamford, CT)
- …of clinical trials and improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, clinical research vendors). Manages ... Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or increasingly complex… more
- Merck & Co. (Rahway, NJ)
- …and SAP team members to further extend capabilities and functionalities on our existing Clinical Trial Supply Management (CTSM) solution in order to satisfy and ... Management and Distribution areas with a strong focus in Clinical Trial Supply Management (CTSM) is highly...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Merck & Co. (Rahway, NJ)
- …of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT).Responsible for project management of the assigned ... environment.Scientific and clinical research knowledge is required.Understanding of clinical trial planning, management and metrics is essential as… more
- Merck & Co. (North Wales, PA)
- …including clinical directors and study managers to lead/support clinical trial scientific-activities.Job ResponsibilitiesResponsible for the clinical ... execution of clinical protocol(s).Serves as the lead clinical scientist on the clinical trial...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …activities in collaboration with the CRO and the study team. Oversee the site qualification process.Monitor clinical trial performance and quality metrics ... disorders. Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good … more
- Merck & Co. (Rahway, NJ)
- …non-traditional therapeutics like peptides, novel biological constructs and others, perform clinical trial simulations, comparator modeling and other model-based ... / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding immunology pipeline.As...analyses to inform dose selection and schedule, clinical trial design and go/no-go decisions.- You… more
- Merck & Co. (North Wales, PA)
- …or related field plus 9-12 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life ... 7 or more years SAS programming experience in a clinical trial environment Department Required Skills and...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Merck & Co. (North Wales, PA)
- …in research activities for innovative statistical methods and applications in clinical trial development.Mentors and guides junior staff in functional ... SAS and/or R.-Good understanding of worldwide regulatory requirements and clinical trial expertise from phase II to...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Merck & Co. (North Wales, PA)
- …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Merck & Co. (Rahway, NJ)
- …translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial simulation, disease progression models, quantitative ... and biologics in Oncology, authoring regulatory documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications… more
- Merck & Co. (Rahway, NJ)
- …development and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process ... of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New Jersey research… more
- Merck & Co. (North Wales, PA)
- …support for anticipated promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates to the ... in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval...working a Hybrid work consisting of three total days on- site per week, generally Tuesday, Wednesday and either Monday… more
- Merck & Co. (North Wales, PA)
- …limited to:Collaborate closely with biomarker scientists and project teams to plan clinical trial biomarker set-up using logistical strategies to ensure ... realm)Preferred Experience and Skills:Drug discovery experience, including familiarity with clinical trial execution in Oncology studiesBiomarker assay… more
- Merck & Co. (Rahway, NJ)
- …measurement and quality-related inquiries from regulatory agencies to support clinical trial and commercial marketing applications.Project Management and ... and molecular interactions with excipients.The Executive Director reports to the Associate Vice President, Analytical Enabling Capabilities and will be directly… more
- Genmab (Cranbury, NJ)
- …opportunities for automation, design and implement solutions, such as automations for Clinical trial agreements, contract management, site management relates ... implemented, and utilized at a pace never seen before. Join Genmab as an Associate Director, Intelligent Automation, R&D Digital Products as part of our IT & Digital… more
- Bristol Myers Squibb (Princeton, NJ)
- …Manager (GTM), Clinical Trial Managers (CTMs) Clinical Trial Monitors (CTMos), Study Start-up Specialists, Site Contract Leads, Vendor Operations ... and non-drug (Lab kits, ECG) importation to support study site + Complete all payment activities including preparing invoices,...work experience. + Experience in the use of industry Clinical Trial Management Systems and Clinical… more
- Lilly (Indianapolis, IN)
- …care, telemedicine, virtual trial orchestration, recruitment & retention, new site models, central clinical services, mobile research, community engagement, ... determined to make life better for people around the world. The Clinical Central Services and Innovation (CCSI) organization is responsible for strategically… more
- University of Utah (Salt Lake City, UT)
- …City, UT **Track** **New Position to Begin** As soon as possible **Details** ** CLINICAL TRIAL AND TRANSLATIONAL RESEARCH , BREAST MEDICAL ONCOLOGY** **Huntsman ... post-doctoral training; 2) Must have an established track record of clinical trial leadership/enrollment and scientific accomplishments with extramural industry… more
- Actalent (Chicago, IL)
- …functional areas on project outcomes and deliverables to meet conflicting demands. Hard Skills + Clinical Trial Registry + Clinical Trial Disclosure + ... Title: Trial Disclosure AssociateJob Description As a Trial Disclosure Associate , you will be instrumental...EU CTR applications and documentation, primarily focusing on the clinical study and site start-up documentation. Your… more
