Clinical Trial Assistant

Real; California (MO); On-site; USD 60,000 - 75,000; Full time

Benefits offered by this job

Health insurance

Health savings accounts

Retirement savings plans

Life and disability insurance

Paid leave where required by law

Job summary

Real is seeking a Clinical Trial Assistant for a 12-month remote contract in the oncology space. The role emphasizes TMF management, site start-up, essential document collection, and cross-functional clinical operations support.

The ideal candidate will have a BS/BA and 3–4+ years in biotech/pharma clinical research, with CTA or Study Coordinator experience preferred and strong MS Office/SmartSheet skills.

Qualifications

• 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.

Responsibilities

• Provide TMF maintenance and site documentation support.
• Assist in site start-up and essential document collection.
• Support study communications and investigator meetings.
• Collaborate with cross-functional clinical operations teams.

Skills

Clinical Research Experience

CTA/Study Coordinator Experience

TMF Management

Site Documentation

Education

BS/BA

Tools

Microsoft Office

SmartSheet

Job description

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

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
• Clinical Research Coordinator (CRC)
• Study Coordinator
• Biotech
• Pharmaceutical Industry
• Remote Clinical Operations

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
• paid leave where required by applicable law

Eligibility may vary based on factors such as location and hire date and is subject to change.