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A day in the life of a Start Up Specialist at Hackensack Meridian Health includes Manages all administrative/regulatory activities associated with start up of Oncology research trials conducted at JTCC including federal, pharmaceutical funded protocols and Investigator Initiated Sponsored Trials as assigned. Facilitates the Review and Execution of Confidentiality Agreemen
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Perform and understand detailed test methods and procedures to include serological evaluation of blood and blood products using traditional methods and Column Agglutination Technology (CAT). Perform in process testing as required by processes and procedures utilizing equipment/instrumentation, such as microscope, blood and blood screening analyzers, calibrated pipettes, c
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Pharmacist, Monmouth Job Locations USA NJ Monmouth Requisition ID 2024 76573 Category Allied Health Pharmacy Pay Range $60.93 $100.62 Pay Range $60.93 $100.62 Company Overview The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to pat
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The Senior Manager, Clinical Data Management is responsible for providing oversight of data management activities to ensure accuracy and consistency of clinical databases for subsequent analysis and reporting. This position is responsible for database development, utilizing EDC system processes and other clinical data applications that allow for internal control of clinic
Posted 1 day ago
The Opportunity Avantor , a Global Fortune 500 company is looking for a dedicated Associate Scientist to optimize our Biopharma / R&D organization. This Bridgewater, NJ on site role is full time. If you have analytical techniques experience let's talk! What we are looking for Minimum Education Bachelor's degree (science focused) Required Experience (1+ yr.) Hands on exper
Posted 1 day ago
At Pentair, you will work along side passionate problem solvers who are committed to the future of our planet. We put our purpose into practice, inspiring people to move, improve and enjoy life's essential resources for happier, healthier lives. From our residential and business water solutions to our sustainable innovations and applications, our 10,500 global employees s
Posted 2 days ago
The Senior Director, Clinical Development Medical Affairs (CDMA) drives strategy and accountability for the hepatology drug program execution, ensuring alignment with brand team objectives, incorporation of relevant internal and external insights and the generation of an R&D plan that delivers for unmet patient need, generates competitive differentiation, and prepares for
Posted 3 days ago
Position Title Associate Principal Scientist, Ingredients Innovation Advanced Research Location Clark, New Jersey (Hybrid) Department Advanced Research, Ingredients Innovation "Do you like working in Advanced Research team, engaging with global raw material suppliers, and contributing to innovation and new product development?" Then L'Oreal Research & Innovation might be
Posted 2 days ago
The incumbent will play a key role in supporting regulatory strategy development and execution of assigned Chemistry, Manufacturing and Control (CMC) Small Molecule programs in the pre approval and/or post approval space globally, as assigned. This position works cross functionally and serves as a liaison between the Regulatory Affairs team and other PTC departments under
Posted 2 days ago
As an active team member of the Computational Biology (CompBio) research group at Boehringer Ingelheim, US research facility in Ridgefield, CT. The successful candidate will contribute to drug discovery efforts through analysis of multiple disease relevant data sets, as well as development of core informatics pipelines and data organization. Responsibilities Strong scient
Posted 2 days ago
Prepares medication orders by compounding or admixing medications under supervision of a registered pharmacist. Checks all orders for completeness of information. Verifies patient information and proper physician authorization. Checks all orders for insurance approval before admixing. Under a professional's supervision, admixes drugs as ordered by physician in an accurate
Posted 3 days ago
General Profile Provides consultation on particularly complex aspects of 'GXP' to project teams and sponsors Drives the implementation of changes required to meet evolving regulatory requirements/industry developments Leads or contributes expertise to process related initiatives Provides support to audits, inspections and Quality Issues, as assigned Expertise Contributes
Posted 1 day ago
A pioneer in K 12 education since 2000, Amplify is leading the way in next generation curriculum and assessment. Our core and supplemental programs in ELA, math, and science engage all students in rigorous learning and inspire them to think deeply, creatively, and for themselves. Our formative assessment products help teachers identify the targeted instruction students ne
Posted 2 days ago
The Associate Director, Regulatory Affairs CMC will be responsible for leading global regulatory CMC strategy for product development and registration, and for preparation of CMC dossier for primarily small molecule regulatory submissions (INDs and NDAs) according to global regulatory expectations and requirements. This position works cross functionally with Regulatory Af
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At Horizon Therapeutics, we define success by the number of lives touched, lives changed, and lives saved. Our global biotechnology company is made up of agile, out of the box thinkers with a focus on delivering breakthrough medicines to those living with rare, autoimmune, and severe inflammatory diseases. This is the heart of our global mission. Start a career that enable
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