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Lennon Stewart
Clinical Program Coordinator
Summary
An experienced Clinical Program Coordinator with extensive knowledge of clinical trial management, GCP regulations, and patient safety. Proven ability to coordinate multisite clinical trials, manage budgets, develop protocols, supervise staff, and ensure data integrity. Seeking a challenging role where I can leverage my expertise to contribute to the success of clinical research endeavors.
Education
Master’s Degree
March 2017
Skills
- Patient Education and Counseling
- Care Plan Development and Implementation
- Disease Management
- Medication Management
- Wound Care
- Patient Advocacy
Work Experience
Clinical Program Coordinator
- Collaborated with investigators to design and conduct clinical studies, ensuring scientific integrity and ethical considerations.
- Prepared and submitted clinical trial documents, including study protocols, investigator brochures, and regulatory submissions.
- Monitored patient enrollment, data collection, and safety reporting, ensuring data integrity and compliance.
- Managed patient recruitment and retention strategies, utilizing various outreach techniques to enroll eligible participants.
Clinical Program Coordinator
- Coordinated multisite clinical trials, ensuring adherence to regulatory guidelines (ICHGCP, FDA, EMA) and ethical principles.
- Managed clinical trial budgets, negotiating contracts with vendors and monitoring expenses to optimize costeffectiveness.
- Developed and implemented clinical trial protocols, ensuring compliance with Good Clinical Practice (GCP) standards.
- Supervised clinical research staff, providing guidance on protocol adherence, data collection, and patient safety.
Accomplishments
- Successfully implemented a streamlined patient intake process, reducing wait times by 25%.
- Developed and implemented a new clinical protocol that improved patient outcomes by 15%.
- Established and maintained strong relationships with healthcare providers, resulting in a 30% increase in patient referrals.
- Coordinated and managed complex clinical trials, ensuring compliance with regulatory guidelines.
- Collaborated with a multidisciplinary team to develop and launch a new clinical program.
Awards
- Recipient of the Clinical Program Coordination Excellence Award for outstanding contributions to the field.
- Recognized with the Patient Advocacy Award for exceptional dedication to patient care within the clinical program.
- Honored with the Research Innovation Award for groundbreaking research in clinical program development.
Certificates
- Certified Clinical Program Coordinator (CCPC)
- Certified Disease Manager (CDM)
- Certified Wound Care Nurse (CWCN)
- Certified Case Manager (CCM)
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How To Write Resume For Clinical Program Coordinator
Highlight your experience in clinical trial management.
Quantify your accomplishments and demonstrate your impact on the success of clinical trials.Showcase your knowledge of GCP regulations.
Use specific examples to demonstrate your understanding of ICHGCP, FDA, and EMA guidelines.Emphasize your skills in patient recruitment and retention.
Describe your strategies for recruiting and retaining eligible participants, and provide data on your success.Proofread your resume carefully.
Make sure your resume is free of errors and that it is well-formatted and easy to read.
Essential Experience Highlights for a Strong Clinical Program Coordinator Resume
- Coordinated multisite clinical trials, ensuring adherence to regulatory guidelines (ICHGCP, FDA, EMA) and ethical principles.
- Managed clinical trial budgets, negotiated contracts with vendors, and monitored expenses to optimize cost-effectiveness.
- Developed and implemented clinical trial protocols, ensuring compliance with Good Clinical Practice (GCP) standards.
- Supervised clinical research staff, providing guidance on protocol adherence, data collection, and patient safety.
- Collaborated with investigators to design and conduct clinical studies, ensuring scientific integrity and ethical considerations.
- Prepared and submitted clinical trial documents, including study protocols, investigator brochures, and regulatory submissions.
- Monitored patient enrollment, data collection, and safety reporting, ensuring data integrity and compliance.
Frequently Asked Questions (FAQ’s) For Clinical Program Coordinator
What is the role of a Clinical Program Coordinator?
A Clinical Program Coordinator is responsible for the day-to-day management of clinical trials. This includes coordinating with investigators, managing budgets, developing protocols, and ensuring compliance with regulatory guidelines.
What are the qualifications for a Clinical Program Coordinator?
Most Clinical Program Coordinators have a bachelor’s degree in a related field, such as nursing, public health, or clinical research. They also typically have experience working in a clinical setting.
What are the key skills for a Clinical Program Coordinator?
Key skills for a Clinical Program Coordinator include project management, clinical research knowledge, communication, and interpersonal skills.
What is the career outlook for Clinical Program Coordinators?
The job outlook for Clinical Program Coordinators is expected to be excellent in the coming years. This is due to the increasing demand for clinical trials and the growing number of new drugs and devices being developed.
What are the top companies that hire Clinical Program Coordinators?
Top companies that hire Clinical Program Coordinators include Parexel, PRA Health Sciences, and ICON.
What is the average salary for a Clinical Program Coordinator?
The average salary for a Clinical Program Coordinator is around $70,000 per year.