Freelance / Contractual CRA, Dermatology / Rheumatology CRO, New South Wales, Queensland areas
Core
Monitor clinical studies at investigative sites to ensure trials are conducted, recorded, and reported in accordance with protocol, SOPs, and regulatory requirements.
Role type
Contractual Clinical Research Associate (cCRA)
Builds
Clinical trial data and site compliance for biotech and pharmaceutical sponsors
Domain
Dermatology and Rheumatology clinical research
Required skills
Site qualification, initiation, and close-out monitoring, Source data verification, Study drug storage and accountability, Regulatory document collection, Patient recruitment support, ICH/GCP compliance
Preferred skills
Dermatology therapeutic area expertise, Autonomous work style, Problem-solving under pressure
Technologies
Microsoft Office (Word, Excel, PowerPoint)
Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits; Prepare site visit reports and follow-up letters; Build relationships with investigators to achieve recruitment targets; Perform source data verification and ensure drug storage accountability.
Seniority
Mid-level, hands-on IC (via careerplan.io/jobs/15-003-1C-270-freelance-contractual-cra-dermatology-rheumatology-cro-new-south-wales-queensland-areas)