- Genmab (NJ)
- …to the effective planning, and timely delivery of complete, high quality and reliable clinical trial data. The Associate Director DM will provide oversight ... activities and processes support the efficient and effective execution of clinical trials.Ensures trial related data management activities (including planning,… more
- Genmab (Plainsboro, NJ)
- …be our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Clinical Trial Manager (GCTM) is accountable for the end-to-end delivery of ... clinical trials from strategy outline through to CSR by leading cross-functional trial specific Clinical Trial Teams (CTT) to deliver clinical trials… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... leader (CSL)Study Planning and Execution: Provides input on major milestones of trial , clinical trial plan and contingency planning; Analyzes and updates… more
- Genmab (NJ)
- …in a therapeutic area for one or more compounds in various stages of clinical development (including clinical trial implementation, and oversight of all ... and timely deliverablesResponsibilities Lead or co-lead one or more complex clinical trial (s) in a therapeutic area for one or more compounds Contribute… more
- Merck & Co. (Rahway, NJ)
- …in database entry systems.Strong knowledge of GCP and GLP.Thorough understanding of clinical research and clinical trial methodologies.Strong regulatory ... Job DescriptionJob Overview:-We are seeking a highly qualified and experienced Associate Director in Data Management to lead our data management team in supporting… more
- Merck & Co. (Rahway, NJ)
- …or related field plus 9 years SAS/R programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life ... Job DescriptionPosition Description: Associate Principal Statistical Programmer - Oncology (Hybrid) In...7 or more years SAS/R programming experience in a clinical trial environmentRequired Experience and Skills: Excellent… more
- Genmab (Plainsboro, NJ)
- …to ensure efficient and effective trial operations.Point of Contact for Global Clinical Trial Managers: Act as the primary point of contact, facilitate ... communication and resolve issues.Vendor Owner:First Point of Contact for clinical trial vendors: Serves as the first point of contact for the vendors, across… more
- Daiichi Sankyo, Inc. (Bernards, 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
- 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 ... related field plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal… more
- Merck & Co. (Rahway, NJ)
- … pharmacology, biomarkers of target engagement, experimental medicine platforms, early clinical trial designs and conduct, and operational understanding for ... Job DescriptionThe Associate Vice President (AVP) will be responsible for...strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development.- The AVP provides strategic oversight for the… more
- Insmed Incorporated (Chicago, IL)
- …strong related experienceOther Pharmaceutical experience - Medical Information, Medical Strategy, Clinical management/ trial experience and 2 years clinical ... a local medical and scientific resource to Insmed for product planning, clinical insights, and intelligence. Capture, synthesize and deliver HCP derived scientific… more
- Merck & Co. (North Wales, PA)
- …and retention efforts to achieve study milestonesUpon request from Global Clinical Trial Operations (GCTO),Recommends study sites and identifies potential ... Job DescriptionRole SummaryThe Oncology Regional Medical Scientific Director ( Associate RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D ... to management and other internal stakeholders Perform regulatory review of all clinical and nonclinical documents for submissions, eg, clinical protocols and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …or similar environment (eg, CRO) requiredOncology, immunology, or complex disease clinical trial experience preferredMust have a strong understanding and ... timelines for assigned studies and escalates issues to the Associate Director of Medical Coding to gain resolution. Functional...MedDRA, and WHO not DD is requiredWorking knowledge of Clinical trial data systems and/or EDC coding… 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
- Actalent (Boston, MA)
- Job Description The Senior Clinical Trial Associate (Sr. CTA) is responsible for supporting the daily workflow of clinical operations activities. The Sr. ... document filing, maintaining study trackers, and oversight of the study-specific electronic Trial Master Files (eTMF). Responsibilities + Serve as a member of the… more
- Lilly (Indianapolis, IN)
- …solutions to support communities through philanthropy and volunteerism. **Purpose** : The Associate Director - Clinical Trial Foundations (CTF), will ... serve as the subject matter expert for clinical systems supporting clinical development. In this...primarily focused on EDC and data aggregation systems. The Associate Director is responsible for collaborating with business partners… more
- Bristol Myers Squibb (Princeton, NJ)
- …drives the development and implementation of innovative strategies and technologies for clinical trial programming. Associate Director develop collaborative ... the development and implementation of innovative strategies and technologies for clinical trial programming + Independently develops, validates, troubleshoots,… more
- US Tech Solutions (Foster City, CA)
- … or related experience in life sciences. * Meets all requirements for Senior Clinical Trial Management Associate (Senior CTMA) grade 26 position with ... required with the collection, delivery and analysis of **biological specimens** within a clinical trial * Provides **sample management** expertise to the Study… more
- Mount Sinai Health System (New York, NY)
- …years of experience in Phase I-IV clinical studies as a clinical trial assistant or clinical research associate is desired. + Excellent Communication ... monitors all safety aspects of clinical research trial (s). Under guidance of the Associate Director...statistics related to dissemination of safety information to the Clinical Trial Management team members and … more
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