Temilade Yesufu
Clinical Research Associate
Indianapolis,IN
Summary
Aspiring clinical research associate with years of experience in pharmaceutical and biotechnology industries. Proven track record of effectively managing and monitoring clinical trials to ensure compliance with study protocols, regulatory requirements, and quality standards. Strong knowledge of good clinical practice (GCP) guidelines and FDA regulation.
Seeking a challenging position of Clinical Research Associate
Results-driven individual with a solid track record in delivering quality work. Known for excellent communication and teamwork abilities, with a commitment to achieving company goals and delivering exceptional service. Passionate about continuous learning and professional development.
Overview
16
16
years of professional experience
Work History
Special Attendant
Neurodiagnostic Institute
Indianapolis, Indiana
07.2024 - Current
- Monitored vital signs and reported any changes to physicians or nurses.
- Assisted clients with maintaining good personal hygiene.
- Actively listened to clients' concerns, questions and feedback regarding services provided.
Clinical Research Associate
Parexel
Durham, NC
12.2023 - Current
- Kept patient care protocols and clinical trial operations in compliance.
- Monitored safety events reported during the course of clinical trials in accordance with SOPs.
- Performed clinical research activities including protocol development, subject recruitment and data collection.
- Participated in educational training, activities, and professional development programs.
- Reviewed site regulatory binder to check collection procedures and completeness of paperwork.
- Checked electronic data capturing systems for integrity and compliance.
- Analyzed collected data for accuracy prior to database lock; identified discrepancies when necessary.
- Achieved project-specific quality and performance standards and provided documentation and communication.
- Evaluated proof of eligibility and consent for participants.
Health Information Management Analyst
Ladoke Akintola University of Technology
Osogbo, Osun
10.2008 - 09.2018
- Adjusted data into necessary formats by using categorization and classification software.
- Put new coding and billing procedures into practice, which helped to reduce number of claims that insurance companies denied.
- Tailored data management plans to specific projects to effectively reach deadlines.
- Developed procedures for organizing and filing clinical data to enhance workflow efficiency.
- Maintained an up-to-date knowledge base of relevant laws, regulations, and industry best practices.
- Collaborated with IT personnel to troubleshoot any technical issues related to EHRs or other software applications.
- Compiled data to enter necessary information into appropriate databases.
- Implemented new technologies such as computerized physician order entry systems in clinical settings.
- Interviewed and hired talented performers, bringing exemplary expertise and knowledge to job positions within organization.
- Provided training to staff on proper use of EHR systems.
- Participated in committees or task forces focused on improving the quality of patient care services.
Monitoring and Evaluation Officer
UNICEF
Osogbo, Osun
03.2012 - 01.2018
- Developed data security and disaster recovery procedures.
- Reviewed and approved project plans prior to implementation.
- Coordinated with external consultants to carry out evaluations as required.
- Established systems for tracking progress against program objectives.
- Facilitated stakeholder meetings to discuss program outcomes, challenges, and solutions.
- Participated in frequent staff meetings to add strategic perspective to day-to-day conversations and programming decisions.
- Analyzed workflows and established priorities for daily operations.
- Collaborated with stakeholders to develop effective monitoring plans and strategies.
- Assisted in developing training materials on monitoring and evaluation topics.
- Drafted evaluation reports based on collected data and analysis results.
- Assessed data processing proposals and requirements to determine project feasibility.
- Contributed towards the development of policies and procedures related to M&E processes.
- Supervised data collection, data quality, analysis, evaluation and dissemination for research projects.
- Conducted field visits to ensure quality implementation of project activities.
- Developed and implemented data collection tools for monitoring projects.
- Maintained updated records of all M&E activities conducted throughout the year.
- Prepared presentations summarizing project progress for management review.
Clinical Research Associate
Mashav Istreal Agency for International Developmen
Tel-aviv, Istreal
10.2015 - 12.2016
- Provided training on GCP standards to new personnel or existing staff members.
- Maintained accurate records of all regulatory submissions, correspondence and approvals received from local ethics committees or regulatory agencies.
- Attained clinical study sponsorships and communicated with sponsor representatives.
- Set up trial sites, which includes ensuring each center has the adequate trial resources.
- Review informed consentform, case report form, investigation drug accountability and adverse events.
- Conduct regular site visits, coordinating projects meetings and writing visiting reports.
- Gathered and reviewed study data.
- Developed and managed budgets for clinical trials according to study protocols.
- Monitored safety events reported during the course of clinical trials in accordance with SOPs.
Education
Virtual Post Graduate Diploma Certificate - Clinical Trial Management
Parexel Academy
Birmingham, MI12-2024
Post Graduate Diploma - Health Promotion
Usual Danfofio University
Sokoto09-2014
Post Graduate Diploma - Hiv/Aids Educational Management
National Open University
Abuja02-2012
Higher National Diploma - Health Information Management/Biostatistics
Obafemi Awolowo Teaching Hospital
Ile-Ife08-2008
Skills
- Medical terminology
- Strong communication
- Proficiency with electronic data capture system
- Detailed documentation
- Regulatory compliance knowledge
- Data analysis
- Source document verification
- Electronic health records
- Ability to effectively interact with study sites and patients
Certification
- Basic Life Support (BLS)
- Electronic Health Records in Nigeria - "Prospects and challenges"
- Health Resource Management and Attitudinal change for productivity
- First International Health Information Management conference for the region of Africa - AHIMA
- Parexel Academy- post graduate certificate in clinical trial management
- Good clinical practice for sites staff and professional version 6
- Late phase studies (IV)
- Industrial Trends in Clinical Monitoring
Timeline
Special Attendant
Neurodiagnostic Institute
07.2024 - Current
Clinical Research Associate
Parexel
12.2023 - Current
Clinical Research Associate
Mashav Istreal Agency for International Developmen
10.2015 - 12.2016
Monitoring and Evaluation Officer
UNICEF
03.2012 - 01.2018
Health Information Management Analyst
Ladoke Akintola University of Technology
10.2008 - 09.2018
Virtual Post Graduate Diploma Certificate - Clinical Trial Management
Parexel Academy
Post Graduate Diploma - Health Promotion
Usual Danfofio University
Post Graduate Diploma - Hiv/Aids Educational Management
National Open University
Higher National Diploma - Health Information Management/Biostatistics
Obafemi Awolowo Teaching Hospital
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