Were looking for a Site Start-Up Clinical Trial Assistant to support key site activation activities and help bring groundbreaking treatments to patients faster. Are you ready to play a vital role in the success of clinical trials
Key Responsibilities
Support SSU team in executing clinical trial start-up activities within timelines.
Assist in drafting and reviewing start-up documents and study plans.
Prepare reports meeting minutes presentations and track documents.
Document and escalate study-related issues to the appropriate manager.
Act as a system/process expert ensuring compliance and efficiency.
Maintain training records and attend required internal/external training.
Participate in process improvement initiatives across departments.
Education
Bachelors degree required preferably in Life Sciences or a related field.
1 year experience in clinical research (Sponsor CRO Vendor or Clinical Coordinator role).
Proficient in Microsoft Teams Word Excel PowerPoint Outlook and SharePoint.
Self-motivated with strong time management and ability to meet deadlines.
Excellent communication & collaboration skills in a fast-paced environment.
Join Fortrea and be part of a dynamic team driving clinical research forward. If youre eager to grow thrive in a fast-paced environment and want to make a real impact wed love to hear from you!
Learn more about our EEO & Accommodations request here.
Required Experience:
Junior IC
Were looking for a Site Start-Up Clinical Trial Assistant to support key site activation activities and help bring groundbreaking treatments to patients faster. Are you ready to play a vital role in the success of clinical trialsKey Responsibilities Support SSU team in executing clinical trial start...
Were looking for a Site Start-Up Clinical Trial Assistant to support key site activation activities and help bring groundbreaking treatments to patients faster. Are you ready to play a vital role in the success of clinical trials
Key Responsibilities
Support SSU team in executing clinical trial start-up activities within timelines.
Assist in drafting and reviewing start-up documents and study plans.
Prepare reports meeting minutes presentations and track documents.
Document and escalate study-related issues to the appropriate manager.
Act as a system/process expert ensuring compliance and efficiency.
Maintain training records and attend required internal/external training.
Participate in process improvement initiatives across departments.
Education
Bachelors degree required preferably in Life Sciences or a related field.
1 year experience in clinical research (Sponsor CRO Vendor or Clinical Coordinator role).
Proficient in Microsoft Teams Word Excel PowerPoint Outlook and SharePoint.
Self-motivated with strong time management and ability to meet deadlines.
Excellent communication & collaboration skills in a fast-paced environment.
Join Fortrea and be part of a dynamic team driving clinical research forward. If youre eager to grow thrive in a fast-paced environment and want to make a real impact wed love to hear from you!
Learn more about our EEO & Accommodations request here.
Required Experience:
Junior IC
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