- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as the Point of Contact (PoC) for gathering country/region specific CDx RA requirements from local RA team members (eg from Japan, China, Australia, Canada, ... retrospective analyses and collection, missing data, demographic/representativeness of samples from clinical trial and screen failures.Clinical trial protocol development… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …necessary information to author the Dose Preparation Instructions and address questions from the clinical sites. The candidate will optimize and continuously improve ... the Pharmacy Manual (PM) template with inputs from internal and external stakeholders. Collaboration with external stakeholders (eg, research pharmacists, clinical… more
- Merck & Co. (Durham, NC)
- …engineering design standards, guidelines and business plan; receives guidance from manager when necessary.Provides & Implements technical guidance to given ... Manufacturing Practices ( GMP)environment.Must be aware of requirement specifications from a qualification perspective (IC/OC, IQ/OQ, CRs, etc.)Actively search for… more
- Merck & Co. (North Wales, PA)
- …non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about Company products. The work of an Regional ... the Regional Medical Scientific Director specific therapeutic area.ResearchUpon request from Global Center for Scientific Affairs (GCSA),Initiates discussions with… more
- Merck & Co. (New York, NY)
- …about non-product areas of interest to the company and replies to scientific questions from SLs, including questions about company products - The work of a Regional ... environment in the Company's Areas of Interest (AOI) - Research Upon request from Global Center for Scientific Affairs (GCSA). Initiates discussions with SLs and/or… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Acts as PCOR Account Lead responsible for leading company response from Deal to Contract (includes pre-deal assessment/analysis, development of business cases ... for National and Regionals accounts of their direct reports leveraging data from multiple sources to understand business complexities to develop the positioning and… more
- Eisai, Inc (San Francisco, CA)
- …and make a difference. If this is your profile, we want to hear from you. Summary: The MSL (Senior Medical Science Liaison or Principal Medical Science Liaison) ... it relates to the business. The Senior/ Principal MSL brings relevant insights from the field on research developments, treatment landscape and new concepts in… more
- Merck & Co. (Rahway, NJ)
- …proper chemistry 8 hour Rotating Shift Work 6AM-2PM, 2PM-10PM, 10PM-6AM Works from verbal and written instructions, governed by special operating procedures received ... from the Watch Engineer. Otherwise works from standard operating procedures Exchanges operating information from previous shift and relays it on to relieving… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …problems and prepares contingency plans and addresses schedule changes resulting from unforeseen events Leads the Admin Council group. Ensures collaboration and ... execution of quarterly Business Review (BRM). Meetings are scheduled from HQ and include participation from the...are scheduled from HQ and include participation from the highest level of NNA/S Executive Management. Responsible… more
- Eisai, Inc (Boston, MA)
- …a fast-paced environment and make a difference. If this is your profile, we want to hear from you. Eisai is in the midst of an important launch of a new product in ... the US focused on educating HCPs on a treatment for appropriate individuals suffering from mild cognitive impairment due to Alzheimer's disease (AD) or mild AD. The… more
- Novo Nordisk Inc. (San Francisco, CA)
- …the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with ... services Supports and assists representatives and managers in answering questions from health care providers and IHNs Combines account management skills, business… more
- Merck & Co. (Rahway, NJ)
- …Pharmaceutical Sciences organization translates molecules to medicines, working from the discovery interface through registration stability manufacturing by ... scaling-up the formulation, device, and manufacturing process. Driving drug product design from the bench top to the Good Manufacturing Practice (GMP) manufacturing… more
- Merck & Co. (South San Francisco, CA)
- …the strategy and process for evaluating therapeutic targets and precision biomarkers from the perspective of genetics, causal disease biology drawing upon a ... edge AI/ML methodsCommunicate complex AI/ML strategies and insights derived from biological data to stakeholders via compelling visualization using state-of-the-art… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …deployed in a sustainable manner Act as a conduit for sharing of best practices to/ from other M2-US or NN teams Lead document control process across site Design & ... degree in Engineering, Business, Communications, or a relevant field of study from an accredited university or an equivalent combination of education & experience… more
- Merck & Co. (Sacramento, CA)
- …practices.Identify and resolve analytical issues, deviations, and out-of-specification results from external testing labs through technical support of investigating ... project timelines and deliverables.Ensure our external testing sites are prepared for inspections from multiple agencies (ie FDA, EMA, PMDA) from an analytical… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …team is focused on redefining health for the millions of people that can benefit from Novo Nordisk medicines in the US. Our priority is to deliver a best-in-class ... redefining health for patients, we look forward to hearing from you. The PositionThe Executive Director, Customer Experience will...competitive and consists of an annual base salary ranging from $222,530 to $389,430. This is determined by multiple… more
- Merck & Co. (Rahway, NJ)
- …and Clinical Supply organization translates molecules to medicines, working from the discovery interface through registration stability manufacturing by designing, ... scaling-up the formulation, device, and manufacturing process. Driving drug product design from the bench top to the Good Manufacturing Practice (GMP) manufacturing… more
- Merck & Co. (Rahway, NJ)
- …& Clinical Supplies organization translates molecules to medicines, working from the discovery interface through registration stability manufacturing by designing, ... up the formulation, device, and manufacturing process.- Driving drug product design from the bench top to the Good Manufacturing Practice (GMP) manufacturing… more
- Merck & Co. (Rahway, NJ)
- …Clinical Supply (PSCS) organization translates molecules to medicines, working from the discovery interface through registration stability manufacturing by ... up the formulation, device, and manufacturing process. Driving drug product design from the bench top to the Good Manufacturing Practice (GMP) manufacturing… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …data integrity issues identified during regulatory inspections, such as those from Quality Events, Audits Findings and Regulatory Inspection (FDA/EMS/ PMDA ... regulatory requirements.Deploy data analytics and ensure that data investigations stemming from systems used for data collection are properly investigated and that… more
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