Freelance /Contractual Clinical Research Associate, Dermatology & Rheumatology CRO, Poland
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 regulatory compliance for biotech and pharmaceutical sponsors
Domain
Dermatology and Rheumatology clinical research
Deliverable
client delivery
Required skills
Site qualification, initiation, monitoring, and close-out visits; Source data verification; Study drug storage and accountability; Regulatory document collection; Patient recruitment support; ICH/GCP standards knowledge
Preferred skills
Dermatology therapeutic area expertise (via careerplan.io/jobs/15-003-09-372-freelance-contractual-clinical-research-associate-dermatology-rheumatology-cro-poland)
Technologies
Microsoft Office (Word, Excel, PowerPoint)
Responsibilities
Conduct site qualification, initiation, monitoring, and close-out visits; Participate in investigators' meetings; Prepare site visit reports and follow-up letters; Build relationships with investigators and site staff; Perform source data verification and ensure drug storage accountability
Seniority
Mid-level, experienced IC