Clinical Trial Assistant

TMF Management

• Site start-up
• Essential document collection
• Study communications
• Investigator meeting support
• Cross-functional clinical operations activities

Requirements

• 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

Desired Skills and Experience

• Clinical Trial Assistant, CTA, Clinical Operations, Clinical Research, Clinical Trials, Trial Master File (TMF), eTMF, Site Start-Up, Site Activation, Essential Documents, Regulatory Documents, Investigator Site File (ISF), Study Coordination, Study Management, Clinical Site Management, CRO Management, Clinical Study Support, Clinical Trial Documentation, ICH-GCP, Good Clinical Practice (GCP), Site Communications, Investigator Meetings, Trial Closeout, Clinical Monitoring Support, 1572 Forms, Financial Disclosure Forms, CV Collection, Vendor Management, Clinical Development, Oncology Clinical Trials, Early Phase Studies, Phase I, Phase II
• Smartsheet, Microsoft Office, Study Tracking, Training Documentation, Inspection Readiness, Document Control

Pay

Details on pay are not specified.

Schedule

Details on schedule are not specified.

Benefits

Details on benefits are not specified.

Company Information

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.