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Toxikon Corporation, originally founded in 1977, is a Contract Research and testing company with laboratories in Bedford, MA and Belgium. Our mission continues to focus on providing quality pre-clinical services, competitively priced, with on-time delivery for the Pharmaceutical, Medical Device and Biotech industries. Toxikon is seeking a Study Director for its Genetic Toxicology group. The Study director has overall responsibility for the technical conduct of safety testing studies according to GLP regulations and represents the principal point of study control for activities related to compliance for in-vitro studies. Responsibilities include but are not limited to: protocol approval, supervision of the conduct of the study experiment according to protocol, documentation of protocol deviations and amendments, reviewing data, conducting and/or approving data analysis, ensuring accurate incorporation of results and conclusions into the study report prior to submission to the Sponsor, working closely with the Sponsor to address study changes, and ensuring archiving of study records. The Study Director is responsible for meeting study timelines and quality standards, and training/mentoring scientific laboratory research associates and/or other junior study directors to department or study specific SOPs. Job Duties and Responsibilities ? 60% reviewing protocols and data generated by the lab ? 20% interaction with clients, sales and other administrative functions ? 20% lab work The main focus for this position is on genetic toxicology studies for pharmaceutical products and medical devices. Experience Required: Ph.D. or M.S. with at least 4 years of experience in in-vitro laboratory work, including cell culture. Desired: cytogenetic, mutagenicity assays, microscopy, cell-based assays, flow cytometry, GLP or regulated environment work. To be successful, the candidate will need to be able to: - Have strong skill in reviewing data and final report, detail oriented. - Have strong organizational skills and work ethic. Maintain accurate schedule and follow-up efficiently. - Communicate clearly and cautiously, both written and oral. - Attain a strong knowledge of GLP regulation and work closely with regulatory affairs on interpretation issues.

This position is located in Bedford, MA.

For additional information about Toxikon go to www.toxikon.com.

Toxikon offers a comprehensive benefits program including: paid vacation sick time, 401(k) plan with company match, medical, dental, vision, life insurance, short and long-term disability insurances, flexible spending accounts, employee assistance program, employee referral bonus, discount programs and more. Toxikon is an equal opportunity employer. As an equal opportunity employer we do not unlawfully discriminate against any applicant because of race, sex, gender, ethnicity, religion, creed, age, color, military/veteran status, genetic condition or information, Family and Medical Leave entitlement, sexual orientation, gender identity, national origin, ancestry, marital status, qualified physical or mental disability, transgender status, or any other legally protected class in accordance with federal, state, and local laws.


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* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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