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Develops and maintains professional relationships with internal and external customers to provide comprehensive medical and scientific support to company initiatives in assigned therapeutic areas. Facilitates information, education, and research activities for physicians and ancillary healthcare professionals regarding current and future therapies in development or commercialized. Works closely with other personnel to ensure information, education, and research needs of healthcare....


The Supplier Relationship Manager manages supplier relationships within the DCP organization to achieve our objectives and in close coordination and collaboration with Procurement, Tech Ops OpU SRMs (for Combination Products):Lead and be accountable to CDA, NDA, MSA, Quality agreement, and supplier agreements Follow business processes and guidelines to act as the center of excellence for legal and financial aspects of the allianceContribute to negotiation of contract terms and conditions,....


The Lead, Human Factors Engineering will be serve as a local leader for the Human Factors Engineering Team as it grows. This role will lead human factors work to support the development of devices and combination products for delivery of our wide portfolio of drugs and biologics. This includes leadership in human factors planning, use-related risk management, requirements development and execution of human factors research (user research, formative and summative studies).1. Responsible for....


Device Development Leader is high impact position for leading development of product device strategy, including technology/platform choice, partner/vendor selection, clinical strategy, regulatory strategy. Requires talented leader with proven expertise in overseeing cross-functional global team activities and to be knowledgeable about overall device development activities. As leader of device development subteam, accountable for device program execution ensuring the translation of product....

- Los Angeles, CA

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

- 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

- 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....

- Any US State

Position Summary: The Senior Director, CMC Regulatory Affairs will be responsible for providing CMC regulatory leadership and strategy across the organization and to our global partners. The Sr Director, CMC Regulatory Affairs will collaborate with the clinical development team, including the Chief Scientific Officer and drug substance and drug product manufacturers, and others for drug development and manufacturing in the pharmaceutical and biotech industry in accordance with the protocol,....

- South Bend, IN

COMPANY BACKGROUND: A research laboratory that has been manufacturing & distributing a variety of enzymes & cofactors used in basic coagulation research for over 30 years is looking for a Technical Specialist to join their team. Their diagnostics division/sister company provides general purpose & specialty assays to the clinical coagulation laboratory; the laboratory incorporates the research laboratories high purity proteins & reagents into clinical diagnostic kits. POSITION....

- Allendale, NJ

Senior MES Engineer Summary: The Senior MES Engineer is responsible for the design, implementation and testing of MES projects primarily for biotech and pharmaceutical clients. Prerequisites: Bachelors of Science degree, preferably in Chemical Engineering or Computer Information Systems is required. A minimum of five years' experience performing batch work, specifically S88 or S95 in FDA regulated industries such as life sciences and food & beverage is required. Prior experience with....


Pharmaceutical company in need of Director or Senior Director to join the Medical Affairs team. The Medical Director will provide support and expertise in the area of psychiatry either Schizo or Addiction as there are two needs In this newly created and high profile role you will serve as the medical affairs strategic lead for our combination oral schizophrenia treatment that is currently in phase 3 clinical development. The Medical Director is expected to establish key medical strategies for....


SENIOR RESEARCH INVESTIGATOR-Liver diseaseRare opportunity to transition from Academia for a specialist in liver disease research. You would work on interdisciplinary teams, where you will function independently in the execution of the experiments but will need to work collaboratively with other team members. Working independently, you will perform design, optimization and implementation of complex in vitro and in vivo experiments in rodents and NHP, and provide cross-organizational support....

- Philadelphia, PA

SENIOR RESEARCH INVESTIGATOR-TRANSLATIONAL RESEARCHRare opportunity to transition from Academia for a specialist in airway/pulmonary disease research. You would work on interdisciplinary teams, where you will function independently in the execution of the experiments but will need to work collaboratively with other team members. Working independently, you will perform design, optimization and implementation of complex in vitro and in vivo experiments in rodents and NHP, and provide....


Position Overview The Sr. Manager will represent Regulatory Affairs for pharmaceutical development projects and marketed products. Working with manager, responsible for development and communication of global regulatory strategy on R&D project teams. Main Areas of Responsibilities The Sr. Manager Regulatory Affairs will ensure technical accuracy and regulatory compliance of all submissions for which they are responsible and ensures that applications are executed appropriately and submitted


We are currently recruiting for a NASH Medical Director, Medical Affairs within Global Medical Affairs (GMA) and the Chief Medical Office (CMO). Working under the leadership of the Global Therapeutic Area Head, this role develops a comprehensive medical strategy for several products in development to treat Non-Alcoholic Steatohepatitis (NASH). They will work closely with Clinical Development colleagues within Research & Development as well as colleagues within Global Evidence & Value....


Job Category: Research & Development The Senior Clinical Program Leader I3 (Inflammation, Immunology and/or Infectious Disease) is accountable for the operational strategy, planning and execution of the clinical development portfolio up to LIP for the designated Discovery and Translational Area (DTA).You provide the primary interface between the I3 DTA and pRED’s the Clinical Program Execution (CPEX) function in Clinical Operations, oversight for program and study management, line....


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....


Medical Affairs – Fully integrated, global biopharmaceutical company developing innovative medicines for the treatment of central nervous system (CNS) diseases. The company has a diversified commercial product portfolio and a substantial clinical pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. In this highly visible leadership role in Medical Affairs, you will work closely with a cross-functional group that includes....


JAVA SOFTWARE DEVELOPER / SOFTWARE ENGINEER / DEVELOPER Columbia, MD REQUIREMENTS:3+ years of current software development experience with the following technologiesJava and/or JavascriptOracle and/or SQL ServerSQLExperience working for a software development product companyStrong Problem solving skillsAbility to understand and translate business requirementsTeam Based AND individual contributor personality ADDITIONAL SKILLS THAT WILL BE USED IN THIS ROLE - IF YOU KNOW THEM ALREADY THIS IS


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....

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