61-80 of 95 results
Sort By


Summary We are currently accepting resumes for the position of Research Scientist in Analytical R and D/Methods Development and Validation. ResponsibilitiesMust be fully capable of developing analytical methods based on experience, literature search, etc.Design, develop, conduct and/or review experiments including method development and methodtransfer; perform methods validations utilizing typical instrumentation including but not limited to LC,MS, GC, etc.Interpret data from routine and....


The Project Engineer is responsible for the development and implementation of control strategies and design to customer application specifications. This position requires an advanced understanding of Emerson products for hardware/software with an in-depth knowledge of advanced programming language and the ability to successfully work in a team environment. PRIMARY DUTIES Ensures that customer's system design and control application requirements are satisfied in a manner that will produce good....


Medical Director for High Profile Pharmaceutical company Looking for an M.D. to work with the Head of Medical Affairs with Immunology / Oncology launch! Contract (or contract to perm). VP would consider an individual from academia - provided they had a strong background in immunology/oncology/hematology or a seasoned Pharmaceutical Professional

- Clinton, NJ

Our client - a growing Pharmaceutical company - is looking for Production Supervisors. These positions are all newly created as a result of an ongoing expansion. The Production Supervisors will be responsible for overseeing the activities of employees engaged in the manufacture of sterile pharmaceutical products. These activities will include preparation, compounding, filling and routine facility monitoring. Additional responsibilities will include:Completing production plan by scheduling and....


Our client - a growing Pharmaceutical Company is looking for three (3) QA Sr. Specialists / QA Specialists. The QA Sr. Specialists / QA Specialists will be responsible for QA and disposition activities in accordance with the Company's policies as well as maintaining compliance with GMP. Responsibilities include the following:Oversee incoming material release and product releaseEnsure maintenance & review of manufacturing batch record documentationProvide document issuance for....


AD, Rare Disease Business Development Reporting to the Head of Business and Corporate Development, this role will serve as a key member of the Corporate and Business Development team, working closely with cross functional partners and the executive management team to advance initiatives that support the corporate vision and goals. These initiatives include buy-side activities, sell-side activities, and corporate strategy projects. The Senior Manager will play a leading role for the strategic....

- San Francisco, CA

Acts as the CEO of assigned early development projects for the assigned division, which may involve managing direct reports. Acts as an expert product developer with proven entrepreneurial ability and mind-set; understanding the scientific, technical, clinical and commercial context for programs from clinical candidate selection (CCS) to readiness for phase III and enabling a seamless transition into later stages of development. Acts as a program champion and is objective and strategic about....

- Newark, DE

Staff Biostatistician (Or Senior Staff - Depending on Level of Experience) Elmsford NY or Newark, DE Competitive Salary, Bonus, 6% 401K, 4 Weeks PTO, Excellent Benefits We have a newly created opening for an experienced Senior (Staff or Senior Staff Level) Biostatistician with a longstanding client; a multi-billion global medical diagnostics/instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized,....

- Elmsford, NY

Staff Biostatistician (Or Senior Staff - Depending on Level of Experience) Elmsford NY or Newark, DE Competitive Salary, Bonus, 6% 401K, 4 Weeks PTO, Excellent Benefits We have a newly created opening for an experienced Senior (Staff or Senior Staff Level) Biostatistician with a longstanding client; a multi-billion global medical diagnostics/instrumentation company. They have strong revenue growth, a stable environment, very low turnover, and offer the opportunity to work on customized,....

- Northern, CA

Responsibilities Manage, develop, and train the GCP Compliance personnel. Ensure the integrity and quality of clinical data by overseeing all routine and directed; internal and external; domestic and international GCP audits and quality reviews. Promote continuous improvements in quality systems and department infrastructure. Act as a subject matter expert and provide GCP guidance to internal departments for all phases of clinical development. Report significant and/or serious ongoing quality....


Our client is a growing global, research-based biopharmaceutical company that combines the focus and passion of a leading-edge biotech with the expertise and capabilities of a long-established pharmaceutical leader to develop and market advanced therapies that address some of the world’s most complex and serious diseases. with approximately 21,000 people worldwide and markets medicines in more than 170 countries Due to expanding product lines and a new standards lab located at Corp....


Represents Regulatory Affairs for pharmaceutical development projects and marketed products. Responsible for development and communication of all aspects of global regulatory strategy on R&D project teams. Leads team of regulatory professionals to assure successful planning and completion of regulatory activities on a worldwide basis. Responsible for knowledge of regulatory requirements of major regions (e.g. US, EU JP) with responsibility for working with colleagues on a worldwide basis....

- Any US State

The role of the Principal Writer, Medical Writing, is to prepare high quality clinical documents and to oversee medical writing responsibilities for multiple programs within an assigned therapeutic area (TA) of Global Branded R&D (including, as appropriate, drugs, biologics, and devices). In this position, the incumbent manages the planning and preparation of high-quality clinical documents (eg, clinical study reports, briefing books, clinical protocols, integrated summaries) and ensures....


Description:Position Title: Director of Business Development- New England Location: Boston, Massachusetts Base increase commensurate with pre-clinical CRO Services sales experience. Travel: Local Territory: Boston, MA with accounts in NH, CT Role: Business Development and Growth of Pre-Clinical Services Comp: OTE $225,000K Potential Year 1, Base $90,000-$140,000 for expertise with the Space. ? Overview: Rapidly growing mid-size Pre-Clinical CRO is expanding into the Boston Market. Productive....

- Bridgewater, NJ

The CTM will work closely with the Director, Clinical Operations and Clinical Development team on the design, execution and oversight of clinical trials (all clinical phases) related to pharmaceutical product development and registration. The CTM is responsible for the overall operational planning and activities for the implementation and conduct of studies (clinical trials, IIT studies, compassionate use and registries) including data management activities, ensuring that clinical studies are....

- Research Triangle Park, NC

Ready to join a team committed to moving gene therapies into the clinical and commercial settings for patients and families devastated by rare neurological genetic diseases? This Client is advancing cutting-edge science to treat rare and life-threatening genetic diseases starting with our clinical-stage, proprietary gene therapy candidate. They are in the midst of an incredible journey, and are looking for passionate individuals to join them on this important mission. Here is your chance to....

- Wayland, MA

Essential Job FunctionsServe as the lead Clinical / Medical Report Writer contributing to a variety of documents for clinical research and regulatory purposes, including clinical research protocols, annual and final study reports, investigator’s brochures, and regulatory submissions including clinical summary reports (CSR), clinical evaluation (CER), and post-market surveillance (PMS) reports.Coordinate the efforts of cross-functional teams to produce high-quality, scientifically accurate....


Global Pharmaceutical company in Madison, NJ is hiring an Executive Director for Clinical Data Management Executive Director, Clinical Data Management is responsible for providing clear vision and strategic direction for Clinical Data Management practices at Company. Planning, directing, and coordinating Clinical Data Management activities including (but not limited to) database specifications development, data management plan creation, data review and reconciliation. The Executive Director,....


OverviewThe company is proud to have been recognized as one of The Boston Globe’s Top Places to Work in 2015, 2016 and 2017. Responsible for leading Process Automation System (PAS) implementation at new Greenfield facility. Work with cross-functional teams on developing system requirements, managing System Integrator project to implement and test, and oversight of all Commissioning and Qualification needs during facility startup. Assist in overall company standards and capital planning around....


Global Specialty Pharmaceutical company in Bridgewater, New Jersey is looking to hire a Manager of Clinical Quality AssuranceThe Manager Clinical Quality Assurance is a key member of the company Research and Development organization. This role is responsible for Clinical QA activity related to the planning, conduct, and reporting of GCP audits in order to ensure that clinical studies are conducted in compliance with applicable regulations, guidelines and company standards. This role also has....

61-80 of 95 results