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Research Scientist II Method Development : Bioanalytical Chemistry | Research Scientist in Researc1

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Research Scientist II Method Development : Bioanalytical Chemistry

Location:
Ashland, OH
Description:

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well:being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. Job Summary Serve as a scientist in the conduct of assigned nonclinical or clinical research studies of moderate to high complexity, to include study management, interpretation, and reporting of study data, and assuring the regulatory compliance of these projects. ESSENTIAL DUTIES AND RESPONSIBILITIES: :Efficiently perform and document all procedures, materials, and results in compliance with applicable regulatory standards as applicable (protocols, methods, SOPs, etc.).:Actively communicate and collaborate across operational areas in order to adhere to timelines and produce quality data.:Independently execute the completion of laboratory investigations, assay troubleshooting, quality observations, and problem solving of technical and/or regulatory issues.:Independently develop and validate quantitative/qualitative methods/procedures with increased complexity/scope in one operational area.:Develop and maintain critical thinking, troubleshooting, and time management skills aligned with needs of operational areas.:Demonstrate effective communication skills through informal discussions with peers, supervisor, and team.:Able to recognize method and/or data issues and communicate them to management to minimize study impact independently.:Independently prepare summary of method development data.:Independently execute review and approval of data for final scientific/technical decisions within a single operational area.:Full understanding of compliance expectations to independently respond to quality assurance audit observations in appropriate software.:Responsible for writing and preparing study plans/protocols/amendments/reports independently.:Independently participate in sponsor visits/tours.:Independently function as liaison, maintaining timely and frequent communication between CRL and sponsor/client/SD.:Independently ensure scientific integrity of studies.:Independently function as a Principal Investigator, Individual Scientist, and/or Study Director as assigned.:Independently write, review, and approve deviations.:Full understanding of regulatory and GLP requirements, industry standards, and company SOPs with the ability to mentor others within one operational area.:Independently manage a portfolio of projects, including method development and validation studies while ensuring timelines are met in a single operational area.:Provide support to staff members as required by operational areas, as needed.:Lead internal process improvements, presentations, and harmonization efforts.:Attend scientific meetings, conferences, and training courses to enhance job and professional skills.:Perform all other related duties as assigned. The pay range for this position is 110:115K. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. Job Qualifications:Education: Associate's degree (A.A./A.S.) or equivalent from a two:year college, preferred. Bachelors degree (B.A./B.S.) or equivalent in a scientific related discipline, recommended. Related Masters degree (M.A./M.S.) or Ph.D./D.V.M., strongly recommended.:Experience: Minimum of 11 to 14 years related experience in the contract research, academic, or pharmaceutical industry.:An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.
Posted:
April 9 on Tip Top Job
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