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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....


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....


Responsibilities:-Must be fully capable of developing analytical methods based on experience, literature search, etc.-Design, develop, conduct and/or review experiments including method development and method transfer; perform methods validations utilizing typical instrumentation including but not limited to LC, MS, GC, etc.-Interpret data from routine and non-routine analyses in order to develop workable test methods and/or deduce and test mechanistic or systematic hypotheses;-Familiarity....


Pharmaceutical company is hiring an Associate Director Medical Writing for their Waltham Massachusetts location.We are a leader in innovative medicines that address the unmet needs and challenges of people living with debilitating diseases. As a fully integrated global biopharmaceutical company, we apply our scientific expertise, proprietary technologies, and global resources to develop products that are designed to make a meaningful difference in the way patients manage their disease. Our....


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....


Position Overview Plans, directs, and executes product formulation and process development activities in support of development of new products intended for clinical trials and commercialization with focus solid and liquid dosage forms including immediate and controlled/modified release systems. Conducts research in the area of formulation sciences in support of innovative product development both for new chemical entities and life-cycle management of marketed products. Experience in the....


High Profile need for Global Pharmaceutical company in NJ Assoc VP, Toxicology company is a bold, global pharmaceutical company and a leader in a new industry Position Overview The Non-Clinical and Translational Sciences organization at Company is seeking an Associate Vice President to lead our department of experienced toxicology/pathology scientists. This role has responsibility for non-clinical safety evaluation for all company pharmaceutical products, in research, development or on the....


Process Controls Engineers with DeltaV experience needed for reputable award-winning Automation and Control Systems Integration company. Great chance to use your industrial automation experience within the Biotech, Pharmaceutical, and Food and Beverage industries. Why work here?:Stable business for 25 years and growing!Fun and professional environment with over 120 employees!Variety of projects in several industries, many pharmaceutical and biotech projects!Training provided on new technology....


Established engineering firm that designs Automation and Controls Systems as well as MEP solutions for plants in the Pharmaceutical, Biotech, Microelectronics, Food & Beverage, and general industrial industries is seeking an Automation and Controls Engineering Leader for their Southern Massachusetts office. Why work here?:Earn shares in the company as you grow with this 100% employee-owned company!Travel is regional and overnight travel is less than 15%!Lead Automation Business Unit for....


Biotech Distribution Sales Specialist My client is expanding and looking to hire a new role in the organization. The Distribution Specialist will take on the following tasks:Drive product sales to all distribution partners and track trends within the territoriesEstablish forecasts and goals for each distributorShare product and operational knowledge to support distributor partnershipsResearch distribution market to provide maximum guidance and support to promote success for each distributor....

- Sacramento, CA

Sales Manager My client is rapidly expanding and seeks to hire a new role -- Sales Manager. The ideal person will take on the following tasks:Develop and successfully manage a team of sales repsAchieve sales goals in prescribed time framePresent sales, revenue and expense reports and realistic forecastsIdentify emerging markets opportunities and market shiftsTranslate client business goals into business deliverablesAnalyze client workflow and provide analysis and metrics to upper....

- Seattle, WA

Biotechnology Sales Representative My client is expanding and seeks a Biotechnology Sales Rep – the ideal candidate will take on the following tasks:Educate and sell the product line to research facilities, pharma and biotech firms and other research institutesExpand business within existing accounts and develop new accountsAssess customer needs and inform researchers and buyers on products Provide extraordinary customer service by guiding the customer throughout the processThe ideal candidate

- Pasadena, CA

Clinical Data Coordinator A newer Biotech company with a growing, innovative, science driven team. As process owner, the Clinical Data Coordinator, manages in-house data management activities (including vendor management) to ensure the accuracy and consistency of clinical databases for subsequent analysis and reporting. In addition, the position is responsible for building programs to create datasets, listings, tables and figures from clinical databases, external data sources, and other....


The Senior Manager, Clinical Development CNS will participate in internal process improvement activities within R&D and Clinical Development. Main Areas of Responsibilities supports the Clinical Program Lead and Clin.Sci. Lead in the development of the Clinical Development Plan and associated clinical trial content (e.g., protocols, IBs/IDFUs, CRFs, CSRs, regulatory submissions and publications) by contributing to scientific/clinical information aligned with the strategy. key Clinical....

- Cambridge, MA

Global Company is hiring a Senior Leader Clinical Operations Biotechnology company specializing in the detailed structural analysis of complex drugs and is headquartered in Cambridge, MA. Company is applying its technology to the development of generic versions of complex drugs, biosimilar and potentially interchangeable biologics, and to the discovery and development of novel therapeutics for oncology and autoimmune indications This position will be responsible for initiating and leading....

- Cambridge, MA

Exciting science being performed at this Pharmaceutical company. Looking to hire two Clinical Operations Leaders under the direction of the New Vice President Clinical.he Clinical Operation Lead is responsible for developing operational strategy for one or more clinical studies, and leading the cross functional Study Management Team to align and deliver on study goals of data quality, timelines, budget and GCP compliance in support of overall program level plans. Responsibilities: The Clinical

- Buffalo, NY

Clinical Project Manager As a Clinical Project Manager (CPM), you will work in a matrix management environment and serve as the primary contact for interdepartmental and external study contacts. This experienced CPM role is responsible for managing all stages of a clinical study within GCP and ICH guidelines when direct management by the sponsor is required. The CPM may also function as the liaison and provide support for sponsor managed studies in an international setting, and, may oversee....


Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study personnel


Clinical Research Associate POSITION OBJECTIVE: Work within a clinical team setting to ensure compliance with protocol and overall clinical objectives. Essential Job Functions/ResponsibilitiesParticipates in the preparation and/or review of draft protocol and informed consent documentsPossesses detailed knowledge of the study protocol and its associated activities and timelinesParticipates in conference calls, prepares agenda and summariesCoordinates with project team and other study personnel


Top Tier Pharmaceutical company (with focus in RESPIRATORY, CNS, Diabetes, Cardio, GI and more) in Madison, NJ is looking for three Clinical Trials Manager Consultants for Clinical Trials Group This is a one year contract and can continue for up to 4 years (1099 or w-2)SummaryParticipate in all aspects of clinical development and study management under the direction of the Director, or designee, which includes providing scientific, and/or logistical support to planned and ongoing trials CTM –....

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