Clinical Research Associate
Posted Jul 17
Posted Jul 17
This is a fully remote position, open to applicants in Pennsylvania.
• Performing site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensuring adherence to protocols, maintaining data integrity, and prioritizing patient safety throughout the trial process.
• Collaborating with investigators and site personnel to ensure effective study execution.
• Conducting data review and resolving queries to uphold the quality of clinical data.
• Assisting in the preparation and evaluation of study documentation, including protocols and clinical study reports.
• A Bachelor’s degree in a scientific or healthcare-related discipline.
• At least 2 years of experience as a Clinical Research Associate.
• Comprehensive understanding of clinical trial processes, regulations, and ICH-GCP guidelines.
• Excellent organizational and communication abilities, with a keen eye for detail.
• Capability to work both independently and collaboratively in a dynamic environment.
• Openness to travel as necessary (approximately 60%).
• Competitive base salary along with performance-related incentives.
• Health and wellness programs, including medical, dental, and vision coverage where applicable.
• Retirement and pension schemes.
• Life insurance and disability coverage.
• Employee assistance programs and wellness resources.
• Opportunities for learning and development through structured training and career pathways.
Worldwide Clinical Trials
Whiteboard Advisors
ClearDesk
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