Clinical Trial Assistant

I'm partnering with an oncology biotech client looking for a CTA. This role will be heavily involved in TMF management, site start-up, essential document collection, study communications, investigator meeting support, and cross-functional clinical operations activities.

Ideal background:

BS/BA required
3-4+ years of biotech/pharma clinical research experience
CTA or Study Coordinator experience preferred
Experience with TMF maintenance and site documentation
MS Office proficiency; SmartSheet is a plus

Details:

12-month contract
Remote
Oncology clinical development environment

EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

In addition to base pay, employees may be eligible for benefits such as health insurance, health savings accounts, retirement savings plans, life and disability insurance, and paid leave where required by applicable law. Eligibility may vary based on factors such as location and hire date and is subject to change.

To find out more about Real, please visit www.realstaffing.com