Open To Work
Olu Gbadebo
Atlanta,GA
Summary
Detail-oriented Clinical Research Associate well-versed in coordinating operations, managing sites and drafting detailed clinical reports. Knowledgeable about action planning, database locking and standard operating procedures. Supports participant recruitment and management to meet research objectives.
Overview
13
13
years of professional experience
Work History
Clinical Research Associate
Allied Clinical Consulting
10.2023 - Current
- Self-motivated, with a strong sense of personal responsibility.
- Worked effectively in fast-paced environments.
- Skilled at working independently and collaboratively in a team environment.
- Proven ability to learn quickly and adapt to new situations.
- Worked flexible hours across night, weekend, and holiday shifts.
- Assisted with day-to-day operations, working efficiently and productively with all team members.
- Managed clinical trial protocols, ensuring compliance with regulatory standards and best practices.
- Oversaw site selection, initiation, and monitoring for multiple clinical studies.
- Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
- Traveled to investigative sites to conduct site qualification, initiation, interim monitoring and close-out visits to maintain and enforce regulatory compliance.
- Enhanced data quality by closely monitoring study progress and ensuring accurate data collection.
- Monitored safety of human subjects and oversaw consent procedures to comply with local and federal regulations.
- Coordinated and scheduled protocol-related visits and required testing to demonstrate vigilance in patient safety, protocol compliance and data quality.
- Ensured protocol adherence, conducting regular site visits and providing training to study staff as needed.
- Conducted meetings with sponsor representatives to discuss clinical study developments.
- Assisted in investigator selection and qualification process to provide capable investigators with adequate resources to properly conduct trials.
- Followed drug storage procedures to comply with protocols and SOP requirements.
- Observed clinical studies and assessed health outcomes in groups of participants to support research plan.
- Mentored team members by sharing suggestions and encouraging ideas to deliver successful studies.
- Created and maintained database and records filing system to document data on specimen collection, processing and storage.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
Clinical Research Coordinator
Grady
09.2020 - 02.2023
- Coordinated clinical trial operations ensuring adherence to protocols and regulatory requirements.
- Managed patient recruitment and retention strategies to enhance study participation rates.
- Developed and maintained study documentation, including informed consent forms and regulatory submissions.
- Collaborated with multidisciplinary teams to streamline project workflows and improve communication channels.
- Oversaw data collection and management processes, ensuring accuracy and compliance with study guidelines.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Developed and managed study budgets, optimizing resource allocation for maximum efficiency.
- Monitored patient recruitment and retention efforts, implementing strategies to improve enrollment rates.
- Collaborated with principal investigators to streamline study workflows and enhance operational effectiveness.
- Maintained accurate documentation of trial-related activities, ensuring data integrity and audit readiness.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Gathered, processed, and shipped lab specimens.
- Followed informed consent processes and maintained records.
- Coordinated and monitored clinical trial activities to support timely and accurate completion of studies.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
- Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
- Increased participant retention rates through proactive follow-up efforts and regular engagement activities.
- Oversaw the management of investigational product supplies, ensuring appropriate storage conditions were maintained at all times for optimal efficacy during trials.
- Reduced data entry errors by implementing stringent quality control measures throughout the study lifecycle.
- Contributed to the successful completion of clinical trials by proactively resolving issues, mitigating risks, and meeting deadlines in a fast-paced environment.
- Implemented electronic data capture system, significantly reducing paper use and increasing data retrieval efficiency.
- Facilitated successful trial completion by closely monitoring study timelines and milestones, ensuring on-time delivery of results.
Business Support Officer
Rig Wells Consulting
06.2019 - 08.2020
- Developed and maintained project documentation to ensure compliance with company standards and client requirements.
- Analyzed client feedback to refine service offerings, resulting in increased customer satisfaction ratings.
- Coordinated training sessions for new staff, fostering knowledge sharing and team collaboration.
- Managed stakeholder communications to align project goals with client expectations effectively.
- Optimized resource allocation by conducting thorough assessments of employee workloads, redistributing tasks as needed to achieve maximum efficiency without sacrificing job satisfaction.
Business Development Associate
Daniel Owen Ltd
05.2016 - 10.2018
- Led initiatives to identify new business opportunities and expand client base.
- Conducted market research to inform business strategies and identify growth trends.
- Collaborated with cross-functional teams to streamline processes and improve efficiency.
- Analyzed sales data to drive decision-making and optimize resource allocation.
- Implemented CRM systems for improved tracking of leads and customer relationships.
- Maintained accurate records of all prospecting activities using CRM software tools for effective lead tracking and follow-up efforts.
IT Support Assistant
Meridian Business Support
07.2013 - 03.2016
- Provided technical support for hardware and software issues, ensuring efficient system functionality.
- Trained new staff on IT protocols and tools, fostering a knowledgeable workforce within the organization.
- Assisted in troubleshooting network connectivity problems, enhancing user experience and productivity.
- Managed inventory of IT supplies, optimizing resource allocation and reducing downtime.
- Documented IT processes and procedures, improving knowledge sharing among team members.
Education
Bachelor of Science - Business And Information Technology
Technological University
Dublin, Ireland06-2013
Bachelor of Science - Biochemistry
Adekunle Ajasin University
Akungba-Akoko, Ondo State, Nigeria07-2006
Skills
- Teamwork and collaboration
- Problem-solving
- Time management
- Multitasking Abilities
- Excellent communication
- Dependable and responsible
- Computer skills
Timeline
Clinical Research Associate
Allied Clinical Consulting
10.2023 - Current
Clinical Research Coordinator
Grady
09.2020 - 02.2023
Business Support Officer
Rig Wells Consulting
06.2019 - 08.2020
Business Development Associate
Daniel Owen Ltd
05.2016 - 10.2018
IT Support Assistant
Meridian Business Support
07.2013 - 03.2016
Bachelor of Science - Business And Information Technology
Technological University
Bachelor of Science - Biochemistry
Adekunle Ajasin University