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Entries tagged with “experience” from BiotechPharmJobs.comThe HR Office, Inc.: Assay Scientist, State College, PA Job Title: Assay Scientist Location: State College, PA Recruiting Firm: The HR Office, Inc. Job description: Our client, a growing biotechnology firm located in Central Pennsylvania, is looking to add a talented individual to their team. Under direction of the Principal Scientist, develop and conduct research studies to enhance performance of existing assays and to develop new assays pertinent to the immunoassay industry. The Assay Scientist will, independently or with the Principal Scientist, develop test designs, perform testing, and analyze complex datasets for summary and documentation. Responsibilities: • Conduct research and development activities according to company goals • Design experiments, analyze data, interpret and summarize results • Perform assay validation under company guidelines, including writing protocols, developing testing plans, execute tests, analyze data and prepare summaries for regulatory applications • Prepare required test solutions and complete calculations of results • Statistical analysis • Interpret results of tests and make recommendations • Operate, maintain and order necessary equipment and supplies • Maintain detailed test documentation and data • Submit device control change documentation • Participate in CAPA and DCC investigations Education / Experience Required:: • MS in Chemistry, Biology, Biochemistry or related field with 5 years of experience in biological, medical, or veterinary sciences or similar scientific field specializing in assay development or characterization of assay performance • Experience in an industrial environment preferred • Equivalent combination of education and experience Additional Requirements: • Proficient in the practice and daily activities of laboratory science • Thorough knowledge of scientific principles and disciplines • Direct experience and comprehensive understanding of immunoassay technology • Technical leadership abilities as an individual contributor If interested, please submit your MS Word resume with salary requirements to lhaft@thehrofficeinc.com An equal opportunity employer, m/f/d/v. Please reference BioTechPharmJobs.com when responding. Makro Scientific: Clinical Program Manager, Swiftwater, PA We at MAKRO deliver custom client-centric solutions by offering contract outsourcing and premium staffing to the most well known IT and Life Science Organizations throughout United States. Our vision is to become a most reliable "connector" between our clients and the Talent pool i.e "YOU." Clinical Program Manager Swiftwater, PA Description: • Defines project standards where necessary to ensure consistency across global projects • Builds effective relationships internally and externally • Manage information on project performance from all team members (including CROs), alerting the Clinical Team Leader and project team to any potential time slippage. • Facilitates resolution of problems affecting the achievement of clinical project milestones • Remain current on trends in individual therapeutic area by attendance at conferences and review of publications Requirements: • BSc with 3-5 years' experience in vaccinology / clinical research • Formal training in GCP methods • Proven track record in delivering high-quality GCP-compliant Clinical Trials • International (ie. more than 1 regulatory environment) Clinical Trial experience preferred • Knowledge of Code of Federal Regulations and regulatory agency documents To apply, please forward your updated MS Word resume, including availability (if you are authorized to work in the United States for any employer), location and position preferences to glenn.davis@makroscientific.com ******** for review before we speak. or contact our Recruitment Helpdesk at 973-679-5005 Also if you have any friends or colleagues, working on similar skill set, kindly refer them as well as there are multiple open positions. An equal opportunity employer, m/f/d/v. Please reference BioTechPharmJobs.com when responding. Makro Scientific: Sr Clinical Data Coordinator, San Francisco, CAWe at MAKRO deliver custom client-centric solutions by offering contract outsourcing and premium staffing to the most well known IT and Life Science Organizations throughout United States. Our vision is to become a most reliable "connector" between our clients and the Talent pool i.e "YOU." Sr Clinical Data Coordinator South San Francisco, CA Description: • Maintain a project-level perspective on data management issues, activities and deliverables • Manage projects resourced externally via contract research organizations or corporate partners • Develop Data Quality (DQ) Plans (specification of the data quality checks that will be performed by Clinical Data Management) • Perform discrepancy management (timely review and resolution of all relevant discrepancies, close interaction with project clinical research associates) • Develop CRFs by interacting with other functional area representatives and managing the physical development of CRFs through Forms Design Requirement: • Strong problem solving skills • Oracle Clinical experience is required, EDC is a plus BA/BS 2-4 years of relevant experience. To apply, please forward your updated MS Word resume, including availability (if you are authorized to work in the United States for any employer), location and position preferences to glenn.davis@makroscientific.com ******** for review before we speak. or contact our Recruitment Helpdesk at 973-679-5005 Also if you have any friends or colleagues, working on similar skill set, kindly refer them as well as there are multiple open positions. An equal opportunity employer, m/f/d/v. Please reference BioTechPharmJobs.com when responding. |
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