Cardiology Clinical Research Associate Resume
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Professional Summary
Dedicated and detail-oriented Clinical Research Associate with over 5 years of experience in managing and monitoring clinical trials in the cardiology field. Skilled in data collection, analysis, and ensuring regulatory compliance. Proven ability to support innovative cardiology research projects and foster successful collaboration among multidisciplinary teams.
Skills
Clinical Trial Management
Data Collection and Analysis
Regulatory Compliance
Project Management
Excellent Communication and Interpersonal Skills
Proficiency in EDC Systems (e.g., Medidata, Oracle Clinical)
Knowledge of Good Clinical Practice (GCP) Guidelines
Work Experience
Senior Clinical Research Associate
Company: AireMixPharmaceuticals
Location: New York, NY
Duration: June 2058 - Present
Lead and monitor various phases of cardiology clinical trials, ensuring adherence to study protocols and regulatory requirements.
Manage the collection, verification, and analysis of clinical data, contributing to high-quality research outcomes.
Collaborate with cross-functional teams, including principal investigators and study coordinators, to facilitate efficient study execution.
Develop and maintain relationships with key stakeholders to ensure project alignment and transparency.
Clinical Research Associate
Company: Forbiz Clinical Solutions
Location: Boston, MA
Duration: January 2055 - May 2058
Conducted site monitoring visits to ensure site compliance with study protocols and GCP guidelines.
Assisted in the creation and implementation of data management plans and case report forms for cardiology studies.
Reviewed and resolved data discrepancies, ensuring the integrity and accuracy of clinical data.
Supported the preparation and submission of regulatory documents for study approval.
Education
Master of Science in Clinical Research
Bachelor of Science in Biology
Certifications
References
Available upon request.
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