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📑 Century Group is partnering with a client who is seeking a Portfolio Reporting Analyst to join their team. Exact compensation may vary based on skills, experience, and location. Expected starting base salary $65, to $68, per year. Job Responsibilities : Produce monthly client sta ...
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📑 Come work at the forefront of science - and help the brands you grew up with grow and evolve into the next generation. Job Description - Principal Scientist, OC Upstream (2407018898W) Principal Scientist, OC Upstream - 2407018898W Description Kenvue is recruiting a Principal Scientist, Oral Care Upstre ...
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📑 Finance Business AnalystFor our client in the digital and IT sector, we are looking for a Finance Business Analyst.Position is to provide support services in a finance ERP Functional team.#J-18808-Ljbffr ...
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📑 Senior Director, Regulatory Affairs*Bay Area- Hybrid*Meet has partnered with a fantastic Bay Area pharma focused in treatments for metabolic, psychiatric, and oncologic disorders. Our client has an approved product and a dynamic late-stage pipeline. You will be coming in to lead their Oncology portfolio and you' ...
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📑 Associate Director/Director, Regulatory Affairs (Oncology)Remote - East Coast CandidatesMeet has partnered with a very well-established pharma with roughly 20 approved products and a robust development pipeline. They are looking for an Associate Director or Director of Regulatory Strategy to join their team. Thi ...
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📑 We are partnered exclusively with an exciting biotech company who are looking to bring on their first hire within their regulatory affairs department. Role can be at Director or Senior Director level.The team are looking for individuals with the following experience:Authoring and submitting an IND (the company i ...
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📑 Immediate need for Regulatory Affairs Specialist with a Clinical Research Organization in Raleigh. Hybrid position - will work partly in office and partly remote. Looking for a Regulatory Affairs Specialist with at least 2 years of regulatory experience along with submissions. Will work on IND submissions (publ ...
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📑 Director, Regulatory Affairs CMCW2 ContractSalary Range: $249,600 - $270,400 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:This position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development a ...
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📑 Director, Regulatory Affairs CMCW2 ContractSalary Range: $249,600 - $270,400 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:This position is responsible for providing CMC regulatory strategies and leading the preparation of CMC sections of regulatory submissions to support the clinical development a ...
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📑 Reference Number: JO-2309-523343Senior Manager Regulatory AffairsRate: NegotiableJob Type: PermanentLocation: United StatesCTR/IND/CTA Regulatory Lead*A clinical stage biotech offering a global lead position working underneath the Senior Director*2023 has seen the business double in s ...
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📑 I am partnered with a Small growing biotechnology company in the San Francisco area that is looking for a Pharmacokinetics expert to join their team! In this position you would be given the opportunity to be the first Pharmacokinetics expert and begin to build out the team along the way. My client is looking for ...
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📑 Clinical Development Leader (Medical Director to Senior Director level)San Francisco (remote/hybrid) **MUST reside on the West Coast or willing to relocate**Full-timeSciPro is working with one of the most exciting names in Oncology. This position holds high visability and will report directly to the CMO.My clien ...
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📑 I am partnered with a Small growing biotechnology company in the San Francisco area that is looking for a Pharmacokinetics expert to join their team! In this position you would be given the opportunity to be the first Pharmacokinetics expert and begin to build out the team along the way. My client is looking for ...
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📑 Job Summary:WHO ARE WE?Live Nation Entertainment is the world’s leading live entertainment company, comprised of global market leaders: Ticketmaster, Live Nation Concerts, and Live Nation Media & Sponsorship. Ticketmaster is the global leader in event ticketing with over 500 million tickets sold annually and mor ...
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📑 AMG is partnering with a prominent national law firm in search of a highly qualified Legal Assistant to join their Intellectual Property Group,with flexibility to work from LA, OC, or SF.Key Responsibilities:Support a team of 3-5 attorneys by preparing and filing various legal documents, coordinating complex doc ...
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📑 Director / Senior Director, Nonclinical SafetyNimbus has an outstanding opportunity for an exceptional Director / Senior Director of Nonclinical Safety (Toxicology) to join our rapidly growing team. This role will lead the safety strategy, from discovery through both nonclinical and clinical stages, and direct a ...
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📑 Reporting to our Senior Director, Drug Product, Process Development, we are seeking an Associate Director to join our team. This position is predominantly a lab-based role and will be responsible for developing scalable processes for LNP delivery of gene-editing RNA cargos. This position will play a critical rol ...
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📑 Molecular Search are currently working with a dynamic and growing CDMO in Maryland, specialising in the development and manufacture of pharmaceutical products and medical devices.Interact with Business Development and Contracts group, Clients, and Operational teams to onboard new projects, identify resources req ...
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📑 A California-based biopharmaceutical company is looking to add an experienced professional to their CMC Quality Control Department as a Writer / Reviewer. In this role, the CMC Quality Control Writer / Reviewer will be responsible for authoring, drafting. reviewing, and approving the Regulatory QC CMC sections o ...
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📑 ** Assoc Dir RA, Boston ** Working on rare diseases, obesity, liver in early and mid-phase compounds for a smaller and stable company with higher visibility from an exclusive leadership teamDo you want to be autonomous in your work and interact closely with the leadership team, to have higher visibility and more ...
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📑 If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Associate Director, Regulatory Affairs CMC Full Time Mgr & Dir - R&D/Ops Malvern, PA, US 10 days ago Requisition ID: 1072 The Associate Dir ...
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