... in Exton, Pennsylvania Senior Quality Assurance GLP Specialist Job title: Senior Quality Assurance GLP Specialist Location: Exton, ... Division/Department: Quality Assurance Reports to: Manager, Quality Assurance Job Summary This position will support Morphotekâ??s Bioanalytical Group Laboratory by providing quality oversight. This individual will be responsible for independent GLP/GMP reviews of test data, validation protocols and reports. Essential Functions Partner with Bioanalytical Group to establish and implement good laboratory practices Develop & implement a laboratory sample tracking system, including resolution of sample issues and retention sample issues Review and approve GLP documents, including data, testing method procedures, change controls, method validation protocols, ...

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Clinical Research Team Supervisor Responsibilities: Coordinates clinical research activities within healthcare network. Provides specialized education concerning research studies and facilitates the conduct of clinical research within healthcare network. Participates in direct patient care. Supervises Study Coordinators and assists Direr of in performance of administrative functions-Performs direct patient care (clinical assessments) in relationship to study protocol demands. Coordinates Protocol information and education among staff nurses, i.e., provides educational and clinical resources and background for study related direct patient care needs. Initiates communication with principal investigators on status of active projects,patient care issues and protocol performance. Determines if patients are suitable fo enrollment ...

... and dedicated colleagues while developing and expanding your career. The CRS is responsible for scientific authoring of clinical protocols, Clinical Investigator's Brochures, Federal Regulatory documents, assisting with Clinical Development Plans, and other scientific documents. Additionally, the CRS is responsible for medical monitoring of data for patients enrolled into clinical studies in real time and in an ongoing basis to review aggregate data for safety and efficacy trends. The CRS operates in a matrix environment to carry out the conduct of specific clinical trials (e.g., oncology). Qualifications ...

... and dedicated colleagues while developing and expanding your career. The successful candidate will work on an interdisciplinary team to deliver siRNA therapeutics, and will be leading a growing group of 8-12 medicinal chemists toward the design and synthesis of new siRNA delivery molecules as therapeutics. They will also lead the structure-activity relationships of these new siRNAs and will be engaged in securing appropriate intellectual property positions for these molecules. He/She will interface between Medicinal Chemistry and siRNA Therapeutics to develop a strategic chemistry plan that takes into ...

... and dedicated colleagues while developing and expanding your career. IPT Manufacturing Support Supervisor / IPT Associate Manufacturing Support Supervisor Support activities in the areas of cost containment, efficiency, productivity, energy conservation, waste minimization, operational excellence and lean practices. Support Lean SIX Sigma transformation of business unit. Support activities directly related to production and scheduling of shop floor observations. Coordinate the implementation of proactive programs to promote environmental and employee safety adherence to Environmental Requirements ...

... and dedicated colleagues while developing and expanding your career. The successful candidate will work on an interdisciplinary team to deliver siRNA therapeutics, and will be leading a growing group of 8-12 medicinal chemists toward the design and synthesis of new siRNA delivery molecules as therapeutics. They will also lead the structure-activity relationships of these new siRNAs and will be engaged in securing appropriate intellectual property positions for these molecules. He/She will interface between Medicinal Chemistry and siRNA Therapeutics to develop a strategic chemistry plan that takes into ...

... and dedicated colleagues while developing and expanding your career. The Medicinal Chemistry group in West Point, PA is currently searching for a Medicinal Chemist to join our team. Within this role, you will work alongside other Merck research scientists and be responsible for the synthesis and identification of organic compounds for biological evaluation against potential drug targets. The successful candidate will be responsible for the synthesis and identification of organic molecules that will be used in the preparation of novel siRNA therapeutics. Knowledge and experience in synthetic chemistry, ...

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The Supply Chain Trial Manager leads all study-related clinical supply activities and is responsible for: Representing Technical Development and Operations (TD & O) at clinical meetings and with CROs Defining distribution requirements and forecasting investigational product Managing contracts with CRO Working with the QA Unit/Qualified Person at CROs to facilitate release Monitoring usage (for example enrollment rates, number of centers added or deleted, protocol amendments) to proactively address inventories and the possible need for additional production, re-labeling or transfer between study sites Developing clinical labeling for multi-country clinical protocols Determining project timelines Accessing the IVRS via the internet and monitor inventory ...

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... Cytometrist - Medical Laboratory near York, PA This job is open as of 11/28/2008. Apply Now! Not a fit for this job? Search other Flow Cytometrist jobs! Are you an employer? Visit us for more info! Email this job to a friend - $1000 Location York, PA; ... Flow Cytometrist, molecular diagnostics, hematological malignancies, medical tech Job Description Do you have at least 2+ years current flow cytometry experience in the area clinical leukemia/lymphoma profiling? If so please read on. The individual will be responsible for the division's clinical flow cytometry testing, assay development, training and implementation ...