IQVIA
Healthcare
ClinicalResearchAssociate
“Clinical Research Associate at IQVIA. Skills: Site monitoring, Oncology studies, Clinical research. Perform site monitoring visits. Adapt subject recruitment plan”
Industry & Context.
Flexibility to travel, Not eligible for visa sponsorship
What They're Looking For.
Must Have
Independent on-site monitoring experience, Oncology therapeutic area experience, Unblinded studies experience, Life science degree educated, Equivalent industry experience
What You'll Do.
Perform site monitoring visits
Adapt subject recruitment plan
Track subject recruitment plan
Administer protocol training
Administer study training
Establish communication with sites
Evaluate site practices quality
Evaluate site practices integrity
Escalate quality issues
Manage study progress
Track regulatory submissions
Track regulatory approvals
Track data query generation
Track data query resolution
Support start-up phase
Ensure site documents availability
Verify Investigator's Site File
Create site management documentation
Create monitoring visit findings
Generate follow-up letters
Generate study documentation
Collaborate with study team
Liaise with study team
How You'll Work.
Team & Collaboration
Study team members
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