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SalaryGeneral Summary:
The Toxicology Senior Research Associate will work to design human and preclinical animal in vitro models to support prioritization and de-risking of novel therapeutic agents throughout the drug discovery and development process. This position will work closely with stakeholders from several functional areas including toxicology, chemistry, DMPK, and research.
Key Duties and Responsibilities:
- Designs, executes, and interprets in vitro safety experiments, with a high degree of reliability
- Culture of complex cellular models for drug screening and proof of mechanism studies
- Contribute to the development and implementation of in vitro safety assays to support the selection and de-risking of potential drug candidates through close interactions with discovery toxicologists, medicinal chemists, and research functions
- Conducts own experimental troubleshooting on routine problems
- Maintains accurate and reliable record keeping including database management, notebooks, and all other pertinent documentation.
- Keeps up to date with current literature in area of expertise and participates in relevant continuing education activities
- Present studies effectively at internal group/department research meetings
- Flexible schedule, including willingness to work intermittent weekends, is required
Knowledge and Skills:
- Demonstrates technical proficiency and skill in planning, executing, and interpreting in vitro experiments
- Knowledge of cell and molecular biology and basic cell culture/sterile technique
- Basic data processing and statistical skills
- Excellent multi-tasking skills, attention to detail and ability to work independently
Education and Experience:
- Masters Degree (or equivalent degree) in Cell Biology, Molecular Biology or related science and 0-2 years of relevant employment experience, or
- Bachelors Degree (or equivalent degree) in Cell Biology, Molecular Biology or related science and 4+ years of relevant employment experience
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (“Vertex”). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements
By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners
If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.
No C2C or Third-Party Vendors
