The Laboratory Coordinator is responsible for coordinating the collection and shipment of oncology clinical trial study specimens per protocol requirements, managing study supplies, and assisting with monitor visits.
Requirements
- 2 years of relevant work experience
- Experience with HIPAA guidelines and research regulations
- Bachelor's degree in biology, chemistry or other science related area (preferred)
- One year laboratory experience (preferred)
- Experience with medical terminology (preferred)
- Oncology experience (preferred)
Benefits
- Coverage for health, dental, and vision insurance on day one
- Health expense accounts with generous employer contributions
- Employer-paid life insurance
- Long-term disability insurance
- Paid time off, including vacation and sick, with ten paid holidays
- Paid discretionary day after six months of employment
- Paid time off for bereavement, jury duty, military service, and parental leave after 12 months of employment
- Retirement program with a generous employer contribution
- Additional voluntary retirement programs (457 or 403b)