- 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 ... Planning and Execution: Provides input on major milestones of trial , clinical trial plan and...CRO / vendors / AROAdditional non-study related activities: Occasional senior management interactions at FIHC, WDC; Initiates contact w/KOL… 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
- Eisai, Inc (San Francisco, CA)
- …customer business, disease state, product prescribing information, approved promotional clinical trials , patient access to medication, and regulatory/compliance ... is your profile, we want to hear from you. Job Summary The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting… more
- Eisai, Inc (Louisville, KY)
- …customer business, disease state, product prescribing information, approved promotional clinical trials , patient access to medication, and regulatory/compliance ... is your profile, we want to hear from you. Job Summary The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director ( Sr . Principal Scientist) has primary responsibility for the strategic planning and directing clinical ... involving investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of … more
- Genmab (Plainsboro, NJ)
- …and/or leading a small team to complete various programming efforts within a clinical trial .You will be responsible for ensuring integrity, consistency, and ... and authentic is essential to fulfilling our purpose.The Role & Department As a Senior Programming Associate or Programming Manager, you will be in the… more
- Aequor (Bothell, WA)
- …SUMMARY:The Downstream Process Development group in Bioprocess R&D is seeking a Senior Associate Scientist contractor to support development and optimization of ... processes for recombinant proteins and biological macromolecules for early- and late-phase clinical trials . The responsibilities of this position include but are… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and leads technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing ... laboratory members, the Contract Manufacturing Organization (CMO), Labeling members and Clinical members. This position works with non-standard problems of some… more
- Eisai, Inc (Nutley, NJ)
- …will also draft and negotiate R&D pharma-related commercial contracts (eg clinical trial agreements, master service agreements, confidentiality agreements, ... regulations and guidance, and corresponding state laws relating to clinical research and development, compliance and liability matters.Knowledge of pharmaceutical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Years related professional experience required.Must have professional experience Project Management, Clinical Supply Management, and/or Clinical Trials ... oriented in the execution of processes, as directed by senior staff, playing a supportive role in ensuring adherence...Import/export requirements to the extent that there is overall recognition of global differences exist and understanding of the… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the application of those principles to trial design, planning & conduct of clinical trials Advanced capability in MS Excel, MS PowerPoint and MS Word ... experience with Supplier Management, Research Administration, Grant Operations, Grant Management, clinical trial management, or a similar research operations… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …actual product Responsible for all areas related to patient safety in clinical trials Act as member of the trial safety group for dose escalation decisions ... within the US East Coast Development Hub comprised of Senior Global Safety Leads, Global Safety Leads and ...) Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Strategic Planning provides strategic insights and direction ... of OBU that will serve as key performance updates to Investor Relations to prepare Sr . Leadership for Earnings calls. The position will play a lead role in ensuring… 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 ... Job DescriptionReports to the Director/ Senior Director in the Office of Promotion and...in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval… 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 ... across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as… more
- Merck & Co. (Rahway, NJ)
- …recent acquisition of EyeBio. One of our key products is currently in Phase 2b/3 clinical trials for the treatment of diabetic macular edema. The product aims to ... excellence, to help people globally. We are currently recruiting for an Associate Vice President (AVP) to lead global marketing for our Global Ophthalmology… more
- Hartford HealthCare (Bridgeport, CT)
- …they turn to us. *Job Summary:* As a specialized research professional the Senior Clinical Research Associate (SrCRA) collaborates with the Principal ... for the overall design, conduct, and management of the clinical trial , the SrCRA leads, facilitates and...all aspects of study activity as required of a Clinical Research Associate This is an onsite… more
- Randstad US (Newbury Park, CA)
- sr associate clinical contracts & budgets....and conduct activities + Manage end to end process for clinical site contracts and clinical trial ... 75 per hour work hours: 9 to 5 education: Associate responsibilities: + Provide clinical site contracting...3 years) contract and budget negotiation experience in a clinical trial setting. + Directly involved with… more
- Lilly (IN)
- … Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and ... methods and innovative validation solutions for use in global clinical trials . The ideal candidate will have...collection systems and associated data repository mappings for a trial or set of trials within a… more
- Abbott (Alameda, CA)
- …people monitor their glucose levels with our new sensing technology. **The Opportunity** The Associate Clinical Research III will assist in the clinical ... required. + Must have 3+ years of relevant experience in site monitoring, clinical trial practices and regulations. + Experience in conducting medical device… more
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