Sr Research Associate (Drug Development & CRO) - Foster City, CA - Onsite
Job Title : Research Associate, Nonclinical Safety
Make sure to apply quickly in order to maximise your chances of being considered for an interview Read the complete job description below.
Location : Foster City, CA - Hybrid 3 days onsite and 2 days Remote
Specific Responsibilities
- Coordinator for high throughput early discovery assays, following templated work instructions.
- Work collaboratively with internal research departments and multi-site CROs to ensure data and reports are received and uploaded to databases in a timely manner to inform project teams on safety liabilities.
- Provide QC review of nonclinical regulatory documents, data tables, study protocols and reports.
- May assist with administrative tasks including document management.
Knowledge, Experience And Skills
- 2+ years of pharmaceutical or CRO industry experience in small molecule and / or biopharmaceutical drug development.
- Must have strong attention to detail and quality of work.
- Ability to prioritize multiple tasks, plan proactively, and meet deadlines.
- Must have strong computer skills such as Word, PowerPoint, and Excel.
- BS or BA degree in scientific discipline.
Top 3 Required Skill Sets
- 1+ years of pharmaceutical or CRO industry experience in small molecule and / or biopharmaceutical drug development.
- Ability to prioritize multiple tasks, plan proactively, and meet deadlines.
- Must have strong computer skills such as Word, PowerPoint, and Excel.
Top 3 Nice To Have Skill Sets
- BS or MS degree in related scientific discipline with 3+ (MS) or 5+ (BS) years of pharmaceutical or CRO industry experience in small molecule and / or biopharmaceutical drug development.
- Knowledge of the general principles and methods of toxicology, animal and human biology and physiology is required.
- Gaining meaningful work experience working at a company with a corporate culture committed to science and patients, and an employee environment that fosters innovation, diversity and a commitment to the personal and professional development of all.
- Gaining extensive knowledge as Study monitor for nonclinical toxicology studies conducted at CROs and responsible for the technical and scientific conduct of studies.
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