- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …rare diseases and immune disorders.Summary Assist in planning and execution of clinical studies , under the supervision of the Study Manager role the Study ... goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities- Reconcile the TMF document… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …equal opportunity employer including veterans and people with disabilities. Summary The Associate Director, Clinical Data Standards, is responsible for the ... improvement opportunities.Communicate and reinforce content and interpretation of Daiichi Sankyo's Clinical Data Standards to DS Project and Study teams,… more
- Spectraforce Technologies Inc (Alameda, CA)
- Job Title: Clinical Research Associate - B Location: Alameda, CA (94502) Shift - 8:00am to 5:00pm Duration: 6 Months with possible extension Payrate starts at ... responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible...Experience: 3-5 Years Experience Level Team Overview: Have 2 clinical managers and 2 study leads. They… more
- Careerbuilder-US (Cambridge, MA)
- …Cambridge ,MA Duration : 12 Months+ Job Description: . The Clinical Research Associate (CRA) in Bio measures, Endpoints and Study Technologies plays a key ... role in assisting the operationalization and execution of internal clinical studies that will be run at...statistics. . Working with the technical lead on collecting clinical study data using mobile/sensor-based technologies of… more
- Russell Tobin & Associates (San Diego, CA)
- …years expeirence in medical device, pharma, IVD and/or CRO 5-8 years experience leading clinical study preparation and monitoring and leading study team ... What are we looking for in our Sr. Clinical Research Associate ? The Scientific Team...Proven track record in clinical study completion with adherence to timelines, budget, and milestones… more
- Careerbuilder-US (Foster City, CA)
- …other Clinical Operations team members in the start-up, maintenance, and close-out of clinical studies . You may manage certain components of clinical ... Job Title: Sr. Clinical Trial Management Associate III (Senior...investigator-sponsored research. You may assist in the review of clinical study protocols and other study… more
- Novo Nordisk Inc. (WA)
- …North America Clinical Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability;… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …product(s) or clinical studies to review and revise CSPs, ICFs, Clinical Study Reports (CSRs), and build and review Statistical Analysis Plans (SAPs) and ... development of minimum core product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …disorders. Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to ... and International Conference on Harmonization (ICH) guidelines. The Senior Clinical Study Manager will have routine interaction... Study Manager role is primarily a tactical study delivery role, reporting into an Associate … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …immune disorders.Summary The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions in the West, ... the timeline, budget and objectives set forth by the Study team.The Clinical Study Manager... Study Manager role is primarily a tactical study delivery role, reporting into an Associate … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- … Associates (SAs) or Senior SAs who assist in planning and in the execution of clinical studies in adherence to the protocol, Good Clinical Practices (GCPs), ... and provide this feedback through regularly scheduled 1:1 meetingsCollaborate with Clinical Study Manager on SA deliverablesParticipates in departmental and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Functional Expertise:Serves as a subject matter expert in medical codingReviews/approves clinical study related documents pertaining to medical coding and ... Position manages the end-to-end delivery of medical coding data for assigned projects/ studies collaborating with clinical and medical teams, CROs and other… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... a living. Are you ready to make a difference? The Position The Associate Director, Research Partnerships (RP) is responsible for developing and executing Real-World… more
- OhioHealth (Columbus, OH)
- …output, walk patients, and answer call lights. We have an Administrative Nurse Manager, Clinical Nurse Manager, and a Clinical Leader for SSU. This position ... Nurse BLS - Basic Life Support CPR - Cardiopulmonary Resuscitation Field of Study : Nursing Years of Experience 0 Work Shift: DayScheduled Weekly Hours : 36Department… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. Summary The Associate Director is responsible for developing RWE strategies for assigned product(s) and execution ... of vendors selected to manage ongoing RWE efforts, including Ph4 study management, and presentations and publications emanating from these effortsActively… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …- Responsible, with limited supervision, for study activities assigned, eg for a clinical study : provide input on the development of study protocol ... The position will act as main statistical contact for the assigned studies , in particular in cross-functional Study team(s).Responsibilities- Study … more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Phase 1 to 3 studies , simulate multiple dose scenarios, and write M&S study report for Phase 1 to 3 studies . This position demonstrates general knowledge ... of Phase 1 studies and multiple dose scenarios, PK/PD M&S analysis data...of disease progression using relatively simple disease modelsWrites MS study reports for Phase 1 to 3 studiesInteracts effectively… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …KPIs, KRIs, KQIs across all RD LFs. Define Cycle Times, Identity key milestones at Study , Country, and Site Level to gauge clinical trial performance. Build and ... and roles. Candidate will be responsible for managing external Benchmarking Study Submissions and seeking out external competitive intelligence to provide line… more
- Merck & Co. (North Wales, PA)
- …as well as statistical support for translational oncology projects and studies .-Interact with Clinical , Regulatory, Statistical Programming, Data Management, and ... responsible for statistical planning and data analysis of Phase I/II oncology clinical trials as well as translational biomarker analyses. This position requires… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionBiologics Process R&D Associate ScientistOur Research Scientists are our Inventors.- Using innovative thinking, state-of-the-art facilities, and ... To achieve this, we work closely with colleagues in Discovery, Pre- clinical , Early Development, Analytical, Formulation, and Commercial Manufacturing while providing… more
