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Global Pharmaceutical company is looking for a Clinical Partnership Liaison Must have pharmaceutical, Biotech or CRO experience at this senior level. located in NYC must work in the office three days/week The Partnership Liaison is a key leadership role within Clinical Operations Business Operations Management. The role is responsible for implementing and driving the success of the Clinical Development sourcing strategy. The role is accountable for Clinical Development alliances with clinical....

- Jersey City, NJ

Pharmaceutical company in Jersey City, NJ in need of Clinical Research Associate Responsible for monitoring of single and multi-site clinical trials. Assures adherence to international Commission on Harmonization (ICH), Good Clinical Practices (GCP), and Code of Federal Regulations (CFR). Assures compliance with institutional Standard Operating Procedures (SOPs) and Policies, protocol requirements, and institutional reporting requirements. Performance of this position requires coordination and


Associate Director Regulatory Affairs Device This bold, global pharmaceutical company and a leader in a new industry model - Growth Pharma. Company is focused on developing, manufacturing and commercializing branded pharmaceutical, device, biologic, surgical and regenerative medicine products for patients around the world. Company markets a portfolio of leading brands and best-in-class products for the central nervous system, eye care, medical aesthetics and dermatology, gastroenterology,....


Principal Scientist GLOBAL PHARMACEUTICAL COMPANY is hiring a Technical lead to design and execute analytical related aspects of pharmaceutical drug product development. Has broad and in-depth understanding of analytical techniques to support testing of a range of small molecules and macromolecules. Understanding of biomolecules and bioanalytical techniques including test methods to support clinical studies such as pharmacokinetics studies is desirable. Has method development/validation....

- Greenville, SC

Reporting directly to the Quality Systems and Compliance manager, the Quality Auditor will have responsibility to audit scheduling, planning, execution and documentation of quality system audits of internal processes for the Greenville location. This position will also be responsible for maintaining a library of standards and for reviewing all applicable regulations, standards and communicating requirements to site leadership. This position will provide cGMP / GXP, technical and auditing....


Pharmaceutical company seeking a Quality Control Chemistry Associate I or II for a position based at their Cambridge, MA site initially with a planned move to Norwood, MA in the May/June timeframe. The individual in this role will perform routine testing of raw materials and samples for mRNA products (in process, release and stability) manufactured at the Norwood, MA facility. Also, this individual may support special projects as assigned. He/she will participate in troubleshooting assays and....


Global Pharmaceutical company is hiring a Director, Scientific Communications- VERY COMPETITIVE base salary, bonus, stock and other Long Term Incentives Succesfull Pharma with marketed products and pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. Headquartered in Dublin, Ireland, Company has an R&D center in Waltham, Massachusetts; a research and manufacturing facility in Athlone, Ireland; and a manufacturing....

- Cambridge, MA

Summary of Key ResponsibilitiesProduce high quality and on-time writing deliverables.Plan, write, edit, and format key documents with minimal supervision, including clinical protocols, investigator brochures, clinical study reports, integrated safety and efficacy summaries and related documents. Other documents may include informed consent forms, health authority briefing books, and scientific publications.Facilitate efficient review and finalization process for documents produced internally....


Two MD contractors needed for Global Pharmaceutical company in Cambridge, MA two roles-Contract Role Only One year contract (renewal up to 4 years), w-2 with benefits offered Has to be office based in Cambridge- we will only consider local candidates at this time. We need PV experience within submissions specifically We have a submission approaching for a product. Need someone with good clinical trial experience. Worked in clinical trial as opposed to post trial setting SPA or European....


Validation Engineer Process Engineer Global Chemical /Biotech company looking to hire: Greenville, Soth Carolina location competitive salary and full relocation and full benefits Would love someone who has: affiliation with: IVT (International Validation Technology), KEN X (Knowledge Exchange Network), PDA, ISPE ResponsibilitiesRemain current on cGMP practices for Process Validation and ensure local Process Validation SOPs and validation documents reflect current industry practices.Provide....

- Somerset, NJ

Specialty Pharmaceutical Company is hiring a Safety Coordinator for Somerset, NJ Competitive Salary, bonus and incentives Provide support for environmental, health and safety matters for the Somerset site including maintaining compliance with federal, state, and local regulations. ESSENTIAL FUNCTIONS: Include the following. Other duties may be assigned. Responsible for coordinating regulatory programs, audits, permits and ensure compliance. Support the development and coordination of all EHS....


Strong Player in the Pharmaceutical Industry is looking to hire a Medical Director for their new Phase one Unit (24 bed) Looking for a true Medical Director (not just a PI) who can interact and engage other Key Opinion Leaders in the Medical Community This role include VERY competitive base salary, long term incentive and full relocation (will make it stress free- pack up, moving and temp housing, real estate assistance and more) The primary responsibilities of this position include medical....

- Decatur, IL

Global Specialty Pharmaceutical company is expanding in their Decatur, IL location Need Process Engineer III will relocate competitive and comprehensive salary and benefits hile a member of the Technical Services organization, the Process Engineer will be located on the manufacturing site located in Decatur, IL. The Process Engineer will be responsible to provide the plant operations unit technical process expertise for a variety of pharmaceutical configurations produced on-site. The scope of....


Global Pharmaceutical Company out of Madison, NJ and Irvine, CA Position Summary: (Irvine, CA or Madison, NJ) Responsible for leading internal and outsourced Clinical Programming activities in support of Clinical Research studies and managing the design, development, validation, implementation, and oversees ongoing support to electronic case report form (eCRF) systems (e.g. InForm, etc.), external data acquisitions, reporting/business intelligence tools (e.g. SpotFire, J-Review), and other....


Global Pharmaceutical and Medical Device company is expanding and in need of a Senior Manager, Process Improvement (manufacturing) New role- must have six sigma and experience in process improvement Must have manufacturing experience, Must have proven change management Must have a very good personality and strong communication skills to effect change with executives but also be relatible to the people at the manufacturing sites Salary is 100k-130k Will relocate , 15%bonus and full benefits....

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