Destiny Heinzig-Cartwright
Oklahoma City,OK
Summary
Dynamic clinical research professional with extensive experience at Lynn Health Science Institute, excelling in project management and staff development. Proven track record in enhancing operational efficiency and compliance, while fostering teamwork and mentoring. Adept at data analysis and strategic planning, contributing to successful clinical trials and improved patient outcomes.
Experienced with managing complex projects and leading diverse teams to achieve organizational goals. Utilizes strategic planning and operational efficiency to drive success. Track record of effective leadership and problem-solving skills that foster collaborative and results-driven environment.
Overview
18
18
years of professional experience
1
1
Certification
Work History
Assistant Director of Clinical Trials
Lynn Health Science Institute
12.2024 - Current
- Supported team members in daily operations, enhancing workflow efficiency.
- Conducted research to inform strategic decisions and improve project outcomes.
- Collaborated with cross-functional teams to align objectives and priorities effectively.
- Managed documentation processes to ensure compliance with organizational standards.
- Participated in training sessions to enhance skills and knowledge of best practices.
- Coordinated communication between departments to streamline project execution.
- Mentored new teachers through observation, feedback, and professional development opportunities.
- Assisted the Director in developing innovative programs to improve students'' academic performance and retention rate.
- Evaluated teacher performance through classroom observations and provided constructive feedback for improvement.
- Oversaw project management, ensuring timely completion within budget constraints.
- Facilitated cross-departmental collaboration to achieve strategic objectives, fostering culture of teamwork and innovation.
- Increased operational efficiency, reviewing and optimizing departmental workflows.
- Improved project outcomes, meticulously planning and monitoring project phases to ensure timely completion.
- Established team priorities, maintained schedules and monitored performance.
- Evaluated employee performance and conveyed constructive feedback to improve skills.
- Established performance goals for employees and provided feedback on methods for reaching those milestones.
- Controlled resources and assets for department activities to comply with industry standards and government regulations.
Certified Clinical Research Coordinator
Lynn Health Science Institute
03.2008 - Current
- Coordinated clinical trial activities, ensuring compliance with regulatory standards and protocols.
- Managed patient recruitment efforts, enhancing participant retention and engagement in research studies.
- Developed study documentation and maintained accurate records to support data integrity and audit readiness.
- Collaborated with cross-functional teams to streamline processes and improve operational efficiency in trials.
- Trained new staff on clinical trial procedures and best practices, fostering a knowledgeable team environment.
- Monitored patient safety and reported adverse events promptly to uphold ethical research standards.
- Implemented quality control measures, ensuring adherence to Good Clinical Practice (GCP) guidelines throughout studies.
- Supported positive relationships between patients and research teams through empathetic communication and compassionate care coordination efforts during clinical trials participation.
- Increased protocol compliance by providing comprehensive training and support to study team members.
- Prioritized participant safety within clinical trials environment via rigorous adverse event reporting procedures compliant with industry regulations.
- Contributed to the advancement of medical research and patient care through the successful completion of numerous clinical trials in various therapeutic areas.
- Optimized efficiency in managing investigational product inventory levels while minimizing waste through meticulous tracking processes.
- Reduced study deviations by closely monitoring patient progress and promptly addressing any issues or concerns.
- Advanced scientific knowledge in the field of clinical research by attending relevant conferences, workshops, seminars, and other educational opportunities regularly.
- Improved data quality by conducting thorough source document verification and ensuring accurate data entry in electronic case report forms.
- Facilitated rapid resolution of complex issues related to study conduct or patient safety concerns through effective problem-solving skills.
- Expedited site initiation visits by working collaboratively with sponsors to ensure all necessary requirements were met prior to study commencement.
- Contributed to the development of new clinical trial protocols by providing expert input on study design, objectives, and methodology.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Followed informed consent processes and maintained records.
- Gathered, processed, and shipped lab specimens.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Collected data and followed research protocols, operations manuals, and case report form requirements.
- Monitored patient safety throughout clinical trials and reported any adverse events.
- Maintained accurate and up-to-date case report forms and source documents for traceability.
- Developed and maintained accurate and up-to-date case report forms and source documents.
Education
Associate of Science - Addiction Counseling
Oklahoma State University
Oklahoma City, OK05.2028
Bachelor of Arts - Psychology
University of Central Oklahoma
Edmond, OK05.2007
No Degree - Nursing
Oklahoma State University
Oklahoma City, OKSkills
- Staff management
- Team operations
- Project management
- Task delegation
- Teamwork and collaboration
- Training and development
- Performance evaluations
Certification
Certified Clinical Research Coordinator, Multiple Cognitive Assessments and Scales, Physical Assessments, Phlebotomy, IATA, Handling/Offering for Transportation of Dangerous Goods, CPR.
Timeline
Assistant Director of Clinical Trials
Lynn Health Science Institute
12.2024 - Current
Certified Clinical Research Coordinator
Lynn Health Science Institute
03.2008 - Current
Associate of Science - Addiction Counseling
Oklahoma State University
Bachelor of Arts - Psychology
University of Central Oklahoma
No Degree - Nursing
Oklahoma State University
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