Overview:
TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi.
Position: Contractor, Nonclinical Safety
Location: Foster City, CA 94404
Duration: 12 Months
Job Type: Contract
Work Type: Hybrid
Description:
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.
Required Years of Experience:
- 1+ years of pharmaceutical or CRO industry experience in small molecule and/or biopharmaceutical drug development
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.
Unique Selling Point of this role:
- 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.
Required Degree or Certification:
- BS or BA degree in scientific discipline.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.
Job Type: Contract
Pay: $34.00 - $38.00 per hour
Expected hours: 40 per week
Experience level:
Medical specialties:
Schedule:
Work Location: In person