- Merck & Co. (Rahway, NJ)
- …concepts, tools, and requirements for all dosage forms (liquid, lyo, drug-device combinations) Review and approval of data and technical documentsAbility to ... This research opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …not limited to CRF/eCRF design, all steps from database development to database release, data review and cleaning, database lock), to ensure data ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...Summary: Position sets the vision, direction, and strategy for Data Management globally and ensures execution of the … more
- Merck & Co. (Upper Gwynedd, PA)
- …to the Sr Director/Director/Principal Scientist/Sr Principal Scientist in Pre-approval Pharmaceutical CMC is responsible for developing and implementing CMC ... regulatory strategies for our company's pharmaceutical pipeline products in accordance with global regulations and guidances, and is-responsible for the preparation… more
- Merck & Co. (North Wales, PA)
- …clinical scientist on the clinical trial team.Leading medical monitoring team in review and interpretation of clinical data /medical protocol deviations in ... Partners with the Study Manager on study deliverables.Ensuring CRF design supports data collection in alignment with the protocol in collaboration with Data… more
- Merck & Co. (Rahway, NJ)
- …interface between our company and our External Partners (EP) for Active Pharmaceutical Ingredients (API) and intermediates. You will be responsible for providing ... diligence assessments and provide expert consultation on chemical manufacturing matters. Review process change requests and deviation reports while ensuring… more
- AUROBINDO (Dayton, OH)
- …group of companies that has a long history of excelling in generic pharmaceutical prouct development and manufacturing. Aurolife has a 10 year history of ... organization has given Aurolife a jump start in building a solid pharmaceutical portfolio very quickly. The Aurolife family consists of an experienced management… more
- Merck & Co. (Rahway, NJ)
- …scientist on the clinical trial team. Leading medical monitoring team in review and interpretation -of clinical data /medical protocol deviations in ... Partners with the Study Manager on study deliverables. Ensuring CRF design supports data collection in alignment with the protocol in collaboration with Data … more
- Eisai, Inc (Nutley, NJ)
- …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... medical affairs personnel to enter strategic and compliant discussions regarding medical/clinical data on Eisai products. The AD assumes a leadership role by… more
- Merck & Co. (Durham, NC)
- …DescriptionAre you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you!The Associate ... to support investigations and develop appropriate CAPAs which lead to program improvements. Review and approve out of tolerance (OOT) records and ensure quality… more
- Tris Pharma (Nashville, TN)
- …live within territory.The selected candidate handles all operational aspects of pharmaceutical sales and service including, but not limited to: generating sales, ... - Bachelors degree and minimum 1 year sales experience in a pharmaceutical , biotechnology, business to business (B2B), capital equipment, medical device and/or… more
- Merck & Co. (Rahway, NJ)
- …11 ComplianceSupport standardization activities for System Development Life CyclePrepare, review , and approve documentation such as master inventory lists, ... for a common goal-Experience in Auditing and Compliance within pharmaceutical industry, including change management and deviation management.Experience supporting… more
- Eisai, Inc (Nutley, NJ)
- …Clinical Programming manages and oversees JReview and SAS program development for clinical data processing, data review reports and listings. This includes ... Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and...support to other areas of Data Operations, Data Management, Clinical Safety Data Review… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …from different disciplines and cultures. Must have technical knowledge on integrated data review and derivation/interpretation of metrics that can dynamically ... variables and processes, and build appropriate mitigations. Drive interface with Integrated Data Review , Data Surveillance, targeted source document… more
- Eisai, Inc (Nutley, NJ)
- …and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... with a primary responsibility of engaging in the exchange of scientific data and other medical and/or scientific information with external customers (healthcare pr… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …/systems SMEs to define reporting needs to oversee process performanceShare and review data /metrics with the GRA Analytics TeamCoordinate the development and ... is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address...This role will be responsible for coordinating the authoring, review and approval of new or updated procedural documentation.… more
- Novo Nordisk Inc. (Los Angeles, CA)
- …activity records/reports, including timely and accurate transmission of call data Participate in relevant meetings, conventions, training programs, and displays ... Maintain up to date knowledge of the latest approved scientific and clinical data to engage in meaningful discussions with customers and address questions, concerns,… more
- Merck & Co. (Rahway, NJ)
- …and contract manufacturing operation (CMO) sites that manufacture active pharmaceutical ingredients (API), biologics, vaccine drug substances and finished products. ... and consultation services for regulatory reporting (eg, BPDR, DPR)Author and/or review global standards and procedures related to biologics, vaccines, and finished… more
- AUROBINDO (Durham, NC)
- …group of companies that has a long history of excelling in generic pharmaceutical product development and manufacturing. Aurolife has a 10 year history of ... organization has give Aurolife a jump start in building a solid pharmaceutical portfolio very quickly. The Aurolife family consists of an experienced management… more
- Novo Nordisk Inc. (Pasco, WA)
- …activity records/reports, including timely and accurate transmission of call data Participate in relevant meetings, conventions, training programs and displays ... by not exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records. Qualifications Bachelor's or equivalent degree, and/or Pharm… more
- Merck & Co. (Rahway, NJ)
- …chain deliverables and prepares, analyzes, and/or develops mitigation strategies for review with clinical partners and senior leaders. -Responsible and accountable ... technical & business risks, & influence portfolio decisions with facts and data -Demonstrates ability to balance strategy with ability for tactical execution and has… more
