Free Clinical Coordinator Assistant Research Resume Template
Clinical Coordinator Assistant Research Resume
Address: [Your Address]
Phone: [Your Phone Number]
Email: [Your Email]
LinkedIn: https://www.linkedin.com/in/your_own_profile
Professional Summary
Highly motivated and detail-oriented Clinical Coordinator Assistant with 3+ years of experience supporting clinical research teams in various healthcare settings. Skilled in data management, regulatory compliance, and patient recruitment for clinical trials. Strong communication skills with the ability to work effectively in fast-paced environments and contribute to the success of research projects.
Skills
-
Clinical Research Support
-
Data Management and Analysis
-
Patient Recruitment and Retention
-
Regulatory Compliance (IRB, FDA guidelines)
-
Electronic Health Records (EHR)
-
Clinical Trial Documentation
-
Team Collaboration and Communication
-
Scheduling and Event Coordination
-
Knowledge of GCP (Good Clinical Practice)
Experience
Clinical Research Assistant
Pinnacle Research Group, Cityville, ST
June 2061 – Present
-
Assisted with managing patient recruitment, scheduling, and follow-ups for multiple clinical trials.
-
Coordinated with principal investigators and research coordinators to ensure the smooth operation of clinical studies.
-
Managed and maintained accurate study documentation and patient data in compliance with regulatory guidelines.
-
Participated in the development and review of study protocols and case report forms (CRFs).
-
Conducted data entry and prepared reports for clinical trial monitoring visits.
Clinical Coordinator Intern
Harborview Medical Research Center, Cityville, ST
January 2060 – May 2061
-
Supported the coordination of clinical trial activities, including patient screening and enrollment.
-
Assisted in organizing research meetings and ensuring that all clinical trial materials were prepared.
-
Helped maintain patient records and ensure compliance with study protocols and regulatory standards.
-
Communicated with participants to ensure their understanding of the clinical trial process.
-
Provided logistical support during clinical study visits and follow-up appointments.
Education
Bachelor of Science in Health Sciences
-
Institution: Cityville University, Cityville, ST
-
Graduated: May 2059
Certifications
-
Certified Clinical Research Coordinator (CCRC) – Expected completion: 2065
-
Good Clinical Practice (GCP) Certified – 2063
Achievements
-
Successfully managed patient recruitment for a clinical trial that exceeded enrollment targets by 15%.
-
Recognized for attention to detail and adherence to protocol compliance in clinical research projects.
-
Received the "Excellence in Research Support" award from Harborview Medical Research Center, Cityville, ST for outstanding contribution to trial management.
