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Greg Martin
Clinical Trial Coordinator
Summary
A highly experienced Clinical Trial Coordinator with a successful track record of managing clinical trials from startup through completion. Proven ability to adhere to Good Clinical Practice (GCP) guidelines and institutional review board (IRB) regulations. Expertise in developing and implementing clinical trial protocols, including study design, subject recruitment, data collection, and analysis. Strong collaboration skills with investigators, clinical research associates, and other healthcare professionals to ensure smooth trial execution. Adept at monitoring and reporting adverse events promptly and thoroughly, ensuring patient safety and regulatory compliance. Proficient in managing budgets and timelines for clinical trials, optimizing resource allocation and ensuring timely study completion. Experience in coordinating patient recruitment and enrollment, screening and onboarding subjects according to study protocols. Conducted site initiation and study closeout visits, ensuring proper documentation and regulatory compliance. Processed and analyzed clinical data, generating reports and providing insights for study investigators and stakeholders.
Education
Master’s in Clinical Research
July 2017
Skills
- Clinical Trial Management
- Data Management
- Project Management
- Regulatory Compliance
- Investigational Product (IP) Management
- Patient Recruitment
Work Experience
Clinical Trial Coordinator
- Managed budgets and timelines for clinical trials, optimizing resource allocation and ensuring timely study completion.
- Coordinated patient recruitment and enrollment, screening and onboarding subjects according to study protocols.
- Conducted site initiation and study closeout visits, ensuring proper documentation and regulatory compliance.
- Processed and analyzed clinical data, generating reports and providing insights for study investigators and stakeholders.
Clinical Trial Coordinator
- Managed clinical trials from startup through completion, ensuring adherence to Good Clinical Practice (GCP) guidelines and institutional review board (IRB) regulations.
- Developed and implemented clinical trial protocols, including study design, subject recruitment, data collection, and analysis.
- Collaborated with investigators, clinical research associates, and other healthcare professionals to ensure smooth trial execution.
- Monitored and reported adverse events promptly and thoroughly, ensuring patient safety and regulatory compliance.
Accomplishments
- Managed a portfolio of 10+ clinical trials simultaneously, ensuring adherence to timelines, budgets, and regulatory requirements
- Developed a comprehensive monitoring and oversight system, reducing protocol deviations and ensuring data integrity
- Successfully recruited and enrolled over 500 participants in a Phase III clinical trial within a tight timeframe
- Collaborated with investigators and site staff to resolve complex issues, optimize study conduct, and maintain compliance
- Implemented a centralized electronic data capture system, streamlining data collection and improving data analysis efficiency
Awards
- Received the Clinical Trial Champion Award for exceptional coordination and management of clinical trials
- Recognized with the Investigators Choice Award for outstanding collaboration and support in clinical research
- Awarded the Excellence in Clinical Trial Management Award for innovative approaches and effective trial execution
Certificates
- Certified Clinical Research Coordinator (CCRC)
- Master’s Degree in Clinical Research
- Certified Associate in Project Management (CAPM)
- Good Clinical Practice (GCP) Certification
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How To Write Resume For Clinical Trial Coordinator
Highlight your experience and skills in managing clinical trials from start to finish.
Be sure to emphasize your ability to adhere to GCP guidelines and IRB regulations.Demonstrate your expertise in developing and implementing clinical trial protocols.
This includes describing your experience in study design, subject recruitment, data collection, and analysis.Showcase your ability to collaborate with a variety of stakeholders.
This includes investigators, clinical research associates, and other healthcare professionals.Emphasize your commitment to patient safety and regulatory compliance.
This includes your experience in monitoring and reporting adverse events.Highlight your experience in managing budgets and timelines.
This includes your ability to optimize resource allocation and ensure timely study completion.
Essential Experience Highlights for a Strong Clinical Trial Coordinator Resume
- Manage clinical trials from startup through completion, ensuring adherence to Good Clinical Practice (GCP) guidelines and institutional review board (IRB) regulations.
- Develop and implement clinical trial protocols, including study design, subject recruitment, data collection, and analysis.
- Collaborate with investigators, clinical research associates, and other healthcare professionals to ensure smooth trial execution.
- Monitor and report adverse events promptly and thoroughly, ensuring patient safety and regulatory compliance.
- Manage budgets and timelines for clinical trials, optimizing resource allocation and ensuring timely study completion.
- Coordinate patient recruitment and enrollment, screening and onboarding subjects according to study protocols.
- Conduct site initiation and study closeout visits, ensuring proper documentation and regulatory compliance.
Frequently Asked Questions (FAQ’s) For Clinical Trial Coordinator
What is a Clinical Trial Coordinator?
A Clinical Trial Coordinator is responsible for the day-to-day management of a clinical trial. This includes tasks such as recruiting and screening participants, collecting and recording data, and ensuring that the trial is conducted in accordance with Good Clinical Practice (GCP) guidelines.
What are the qualifications to become a Clinical Trial Coordinator?
A bachelor’s degree in a related field, such as nursing, health science, or clinical research, is typically required. Additionally, certification from a professional organization, such as the Association of Clinical Research Professionals (ACRP), is highly recommended.
What are the job responsibilities of a Clinical Trial Coordinator?
Clinical Trial Coordinators are responsible for a variety of tasks, including: recruiting and screening participants, collecting and recording data, ensuring that the trial is conducted in accordance with GCP guidelines, and monitoring and reporting adverse events.
What are the career prospects for a Clinical Trial Coordinator?
Clinical Trial Coordinators can advance to a variety of positions, such as Clinical Research Associate, Project Manager, or Clinical Trial Manager.
What are the challenges of being a Clinical Trial Coordinator?
Clinical Trial Coordinators face a number of challenges, such as: recruiting and retaining participants, ensuring that the trial is conducted in accordance with GCP guidelines, and managing the workload.
What are the rewards of being a Clinical Trial Coordinator?
Clinical Trial Coordinators can experience a number of rewards, such as: making a difference in the lives of others, working in a challenging and rewarding field, and having the opportunity to learn about new medical treatments.