Research Analyst

• Monitor on-site and remotely clinical trials in accordance with TFS and/or sponsor Standard.
• Perform all required monitoring activities at the study sites to assess and ensure subjects safety, data integrity and quality.
• Verify the protection of study participants by informed consent procedures and protocol requirements that follow appropriate regulations.
• Review CRFs (electronic or paper) and subject source documentation for validity and accuracy.
• Verify proper management and accountability of Investigational Product.
• Timely reporting of actions taken during monitoring visits in Monitoring Visit Report including findings, corrective and preventive actions already taken and update applicable tracking systems, as required; escalate observed deficiencies and issues as appropriate.
• Monitoring Close-out visits in Ukraine.

Senior Clinical Research Associate – Freelance

• You will be dedicated to a single client.
• You will be responsible for all site management and supervisory activities in the assigned oncology studies.
• You will work with industry leaders and subject matter experts.
• You will have the opportunity to mentor junior CRAs.
• You will work with world-class technology.
• You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.

Senior Clinical Research Associate

• You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
• Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborating with investigators and site staff to facilitate smooth study conduct.
• Performing data review and resolution of queries to maintain high-quality clinical data.
• Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Clinical Research Associate II – Senior Clinical Research Associate

• Independently plan, conduct, and follow up on pre-study, site initiation, routine monitoring, and close-out visits, both on-site and remotely, in line with the applicable monitoring plan
• Oversee study site performance, including recruitment progress, and provide ongoing support to sites on study-related questions and operational issues
• Review eCRF data, timelines, and queries; identify and report protocol deviations; and maintain clear communication with project management and sponsors
• Review and maintain study documentation at site level, including Investigator Site Files (ISF), ensuring inspection readiness and compliance with applicable regulations
• Collaborate cross-functionally with medical, project management, quality management, and data management teams, and support sites during audits and inspections

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Senior Clinical Research Associate – Freelance

Senior Clinical Research Associate

Clinical Research Associate II – Senior Clinical Research Associate

Senior Clinical Research Associate