Freelance SCRA: Expert Site Monitoring & Oversight

ProPharma; Finland; Hybrid; EUR 70,000 - 110,000; Full time

Job summary

ProPharma is seeking a Freelance SCRA to support Finland-based studies. The role involves monitoring assigned sites, ensuring protocol adherence, and managing regulatory documentation in line with GCP and SOPs.

Responsibilities include on-site and remote monitoring visits, data integrity checks, and collaboration with cross-functional teams to support study start-up activities and site tools development.

Qualifications

• Bachelor's degree or equivalent combination of education and experience.
• > 5 years of experience as a Clinical Research Associate.
• Experience monitoring clinical sites and handling regulatory documentation.

Responsibilities

• Monitor assigned clinical sites and write monitoring reports per SOPs and regulatory requirements.
• Conduct site initiation, interim and close-out visits, in person and remotely.
• Support site start-up activities and regulatory submissions as needed.
• Review source documents and case report forms for accuracy and integrity.
• Coordinate regulatory documentation and site tools for monitoring activities.

Skills

Verbal and written communication

Microsoft Office

EDC

CTMS

IVRS

eTMF

Regulatory knowledge (GCP/ICH)

Prioritization and planning

Site management and training

Education

Bachelor's degree or equivalent

Tools

Microsoft Office

EDC

CTMS

IVRS

eTMF

Job description

ProPharma is seeking a Freelance SCRA to support Finland-based studies. The role involves monitoring assigned sites, ensuring protocol adherence, and managing regulatory documentation in line with GCP and SOPs.

Responsibilities include on-site and remote monitoring visits, data integrity checks, and collaboration with cross-functional teams to support study start-up activities and site tools development.