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Clinical Research Associate/Senior Clinical Research Associate

Remote:

Full Remote

Experience:

Mid-level (2-5 years)

Work from:

France

Offer summary

Qualifications:

BA/BS in health or science-related field, Minimum 2 years clinical trial monitoring experience.

Key responsabilities:

Ensure adherence to SOPs and regulatory requirements
Manage site initiation, monitoring, and close-out activities
Provide accurate data by resolving queries promptly
Report and document AEs/SAEs/PQCs timely
Maintain data accuracy for inspection readiness

KellyOCG

1001 - 5000 Employees

See more KellyOCG offers

Job description

Your missions

Note: This role is expected to potentially open in October. We are currently pipelining candidates for this position.

Location: Europe

Ready to take your Clinical Research expertise to the next level? Join Kelly FSP and potentially support one of the world's top five pharmaceutical companies in driving innovation and advancing healthcare. As a Clinical Research Associate located in EMEA, you'll play a key role in ensuring compliance with global standards. Apply now and let's make a difference together!

Key Responsibilities:

Compliance: Ensure adherence to SOPs, WIs, policies, and local regulatory requirements.
Site Management: Act as the primary contact for trial sites, managing site initiation, monitoring, and close-out.
Data Quality: Ensure the provision of accurate, valid, and complete data by sites, resolving queries within expected timelines.
Subject Safety: Ensure timely reporting and documentation of AEs/SAEs/PQCs.
Inspection Readiness: Maintain complete and accurate data and documents for inspection readiness.

Qualifications:

Education: BA/BS in a health or science-related field or equivalent industry experience.
Experience: Minimum 2 years of clinical trial monitoring experience; 3 to 5+ years for senior roles.