Clinical Research Associate - Remote

Overview

The Clinical Research Associate (CRA) is responsible for executing clinical monitoring activities at clinical trial sites, ensuring compliance with ICH guidelines, GCP, and local regulations while contributing to the success of oncology/hematology clinical trials.

In Short

• Execute clinical monitoring activities at trial sites.
• Monitor clinical trials in accordance with ICH guidelines and GCP.
• Perform feasibility, site identification, and evaluation.
• Conduct monitoring visits and complete reports.
• Manage site performance and ensure timely delivery of study milestones.
• Provide training to assigned sites on protocols and studies.
• Identify gaps and propose corrective actions.
• Ensure inspection readiness of studies and sites.
• Collaborate with regional managers and clinical sites.
• Travel up to 60% for site monitoring.

Requirements

• 2+ years of CRA monitoring experience in the pharmaceutical or CRO industry.
• Thorough knowledge of clinical trial processes and regulations.
• Excellent communication and interpersonal skills.
• Strong organizational skills and ability to prioritize tasks.
• Fluent in English (writing and speaking).
• Efficient in Microsoft Word, Excel, MS Project, PowerPoint, and Outlook.
• Ability to identify and resolve site issues proactively.
• Demonstrated initiative and entrepreneurial mindset.
• Commitment to continuous learning and embracing change.
• Results-oriented with strong analytical thinking skills.

Benefits

• Opportunity to work in a rapidly growing oncology company.
• Collaborative and inclusive work environment.
• Commitment to diversity and equal opportunity employment.
• Engagement in innovative treatments for cancer patients.
• Global reach with a team across six continents.