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- 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


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....


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


The Director of Maintenance and Engineering, under the supervision of the Site Leader has direct responsibility of the overall site and related equipment including two separate facilities in a single campus environment encompassing approximately 300,000 sq. ft. Areas of responsibility include project management of all significant site projects utilizing both internal staff and outside contractors, maintenance and procurement input on all equipment related needs for both manufacturing and....


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....


POSITION SUMMARY: Independently responsible for the efficient and thorough investigation of process deviations and customer complaints, determination of root cause, and initiation of corrective/preventative actions designed to adequately address and correct the Quality related deficiencies identified during the investigation process. Responsible to provide proactive corrections based on noted trends to minimize the potential for repeat incidents that may lead to, or result in, the issuance of....


Accountabilities and Responsibilities: - Engage and lead local IT team resources and business personnel to plan, implement, and support local as well as enterprise IT, laboratory, and business systems. - Be an integral member of multiple global IT and system teams, planning and implementing a global IT vision and infrastructure. - Exercise project management of local IT projects, including schedules, updates, meetings, documentation, resources, and completion milestones. - Proactively....


POSITION SUMMARY The Analytical Instrumentation Manager will be responsible for the management of daily activities in support of all analytical equipment in Quality Control. The manager will assure that activities associated with the testing, release and results reporting of materials, products and components meet established and expected quality, Data Integrity requirements, regulatory and customer requirements. The Manager will regularly interact with departments on site and at a corporate....


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....


The Director, Clinical Pharmacology acts as the primary clinical pharmacology lead providing clinical pharmacology expertise to a multidisciplinary study team. The Associate Director/Director, Clinical Pharmacology is responsible for clinical pharmacology programs for assigned projects and will be the key expert on all clinical pharmacology & pharmacometrics matters relating to assigned projects. The Associate Director, Clinical Pharmacology will work in close collaboration with different....


Reporting to the Vice President, Drug Development-Generics, the Director, Project Management will use the global PDP (Product Development Process), allied systems & tools, to plan and manage/coordinate resources and activities related to product development and maintenance of business projects throughout Global R&D, and other company organizations. Responsibilities: Responsibilities:Champion and lead projects for new generic product development.Management of project team members from....


POSITION OBJECTIVE: The Senior Manager, Clinical Supply will be responsible for end-to-end drug supply planning activities across the Client clinical portfolio and for leading the clinical drug supply team. Responsibilities include forecasting supply requirements across the clinical portfolio and managing IP (Investigational Product) production and distribution process on time, with good quality, in compliance with Health Authority regulations/guidelines and Client SOPs. Collaborates and....


My CLIENT, is a New Jersey based, stable, not-for-profit biomedical research organization devoted to developing drugs that will slow the progression of neurodegenerative disease (NDD) and provide meaningful clinical benefit to patients. They are seeking a junior, but highly motivated and organized individual to assist their Science Directors managing projects in the clinical portfolio (including, but not limited to clinical studies and trials). They want a Bachelors or Master’s degree in life....


Microbiologist - Lab Technician – near Charleston, SC Leading producer of specialty grade phosphate products used in the Pharmaceutical and Industrial markets is seeking a Microbiology Lab Technician. This company takes pride in producing quality products for the industries they support. They are seeking an individual with high integrity and very detail oriented. What the company offers:Competitive salaryMedical, Dental, and Vision insurance options.401K with a match of dollar to dollar of....


POSITION OBJECTIVE: Responsible for leading the CMC (Chemistry, Manufacturing and Controls) regulatory function, the Senior Manager, Regulatory CMC will collaborate cross-functionally to develop the CMC regulatory strategy, provide guidance to broader CMC functions, and drive CMC regulatory filing(s). Working collaboratively with senior leadership to develop CMC regulatory strategies for one or more investigational and/or commercial products this position will lead the preparation and filing....


POSITION OBJECTIVE: The Director of Clinical Pharmacology and Drug Metabolism and Pharmacokinetics (DMPK) is responsible for overseeing internal and external activities associated with understanding the absorption, distribution, metabolism and excretion properties of multiple drug candidates in preclinical and clinical development. The person will play an active role on cross-functional program teams, this includes planning development strategies and interpreting data, as well as making....


Job Description Job Title: Director, Pharmacy Standards Reports To: Senior Director, Pharmacy Operations FLSA Status: Exempt Department: Pharmacy Services Location: corporate office near Nashville, TN Summary: Provide information system management in order to manage, plan, communicate, and support company standardized medication use strategies including formulary management, clinical initiatives, interdisciplinary clinical collaboratives, and other medication use policies and standards.....


Our client seeks a Clinical Research Operations professional to plan their Phase I Clinical Trials Requirements Bachelor’s Degree in life sciences or healthcare field. Additional coursework in clinical trial design.Ability to travel as required (up to 25%).12+ years of proven experience in clinical research and/or clinical trial operations, including a minimum of 7 years in a supervisory role managing (internal/external) clinical operations staff.Industry experience within pharmaceutical....


The Regional Sales Manager is responsible for managing the sales representatives and the sales activities of the Particle Characterization, Rheology, and Nanomaterials Testing product lines within the Western Region (eleven western states). This position reports to the Regional Vice President. Responsibilities & QualificationsAssists the Vice President of the region to build sales territories within assigned region.Interviews, makes hiring and firing recommendations, develops new hires,....

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