Adejoke Adijat Joseph
Milton Keynes,BKM
Summary
Versatile clinical research professional who is knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning , good project management and problem-solving abilities. A detail-oriented team player with strong organizational skills and an impeccable ability to handle multiple projects simultaneously with a high degree of accuracy. Organized and dependable at managing multiple priorities with a positive attitude, and always willing to take on added responsibilities to meet team goals. A full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills is desired.
Overview
9
9
years of professional experience
1
1
Certification
Work History
Senior Clinical Trial Study Lead
Bioluminux Clinical Research
12.2023 - Current
- Managed and monitored clinical trial sites as per protocol, study-specific data safety monitoring plan, ICH/GCP guidelines, sponsor SOPs and processes.
- Managed project activities compromising study start-up activities, site initiation, monitoring, close-out, and database locks.
- Assist in protocol, Informed Consent, and CRF design and review.
- Verify subject safety and site adherence to FDA Regulations, sponsor requirements, and ICH/GCP Guidelines
- Mentored office employees on proper procedures, keeping operations consistent and efficient for maximum performance.
- Established strong relationships with clinical site personnel, promoting open communication channels for resolving concerns or clarifying questions throughout study duration.
- Maintained high level of ethical conduct throughout all aspects of clinical trials, ensuring adherence to Good Clinical Practice guidelines and other relevant regulations.
- Developed comprehensive training materials for new team members, expediting their integration into ongoing projects without compromising quality standards.
- Reduced discrepancies in data collection by creating user-friendly electronic case report forms tailored to each specific trial protocol.
- Streamlined trial processes with creation of detailed study-specific procedures and guidelines.
- Managed essential document storage, ensuring compliance with regulatory requirements and easy access for audits or inspections.
- Achieved timely completion of study milestones by closely monitoring trial progress and addressing potential roadblocks.
- Regularly reported study progress updates to senior management, facilitating informed decision-making regarding resource allocation or strategic direction changes as needed.
- Ensured data accuracy by meticulously reviewing and maintaining case report forms and source documents.
- Mentored junior team members, fostering collaborative work environment that encouraged ongoing professional development and growth.
- Led site initiation visits to train staff on study protocols, paving way for successful trial execution.
- Enhanced patient enrolment by developing and implementing effective recruitment strategies for clinical trials.
- Screened patient records, databases, and physician referrals to identify prospective candidates for research studies.
- Maintained compliance with protocols covering patient care and clinical trial operations.
- Gathered, processed, and shipped lab specimens.
- Followed informed consent processes and maintained records.
- Complied with research protocols by providing ongoing quality control audits.
- Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
Clinical Lecturer/ Honorary Hospital Consultant
University Of Medical Sciences
08.2017 - 10.2022
- Developed and implemented innovative teaching strategies to engage students in lectures and coursework.
- Evaluated and revised lesson plans and course content to achieve student-centered learning.
- Cultivated critical thinking skills through challenging assignments that required analysis, synthesis, and evaluation of information from various sources.
- Participated in conferences and professional development opportunities to stay up-to-date with latest trends in field.
- Evaluated student progress through regular assessments, providing detailed feedback for improvement and growth.
- Developed strong relationships with colleagues, collaborating on curriculum development and sharing best practices in teaching strategies.
- Conducted individual research projects to actively contribute to institution's research work.
- Used PowerPoint and Google Classroom technology to give presentations to student classrooms.
- Collaborated with faculty and staff to create meaningful learning experiences.
- Selected and designed lesson plans and curriculum to meet academic objectives.
- Led seminars and workshops to facilitate student learning and engagement and increase memory retention.
- Promoted collaboration among students through group projects and presentations, fostering teamwork and communication skills.
Clinical Lecturer/ Honorary Hospital Consultant
Bowen University/ Bowen University Teaching Hospital
09.2015 - 08.2017
- Developed and implemented innovative teaching strategies to engage students in lectures and coursework.
- Streamlined internal processes to enhance team efficiency and improve overall project outcomes.
- Evaluated client needs and expectations, establishing clear goals for each consulting engagement.
- Developed strong relationships with students, parents, and colleagues by maintaining open lines of communication and fostering supportive learning environment.
- Maintained up-to-date knowledge on best practices in HIV case management through continuous professional development opportunities such as trainings, workshops, and conferences.
- Coordinated and organized individual and group skill building opportunities to foster adherence to medications and identify strategies to improve adherence to health routines.
- Ensured compliance with regulatory requirements through meticulous record-keeping and reporting practices.
- Provided detailed project status updates to stakeholders and executive management.
Education
Master of Science - Clinical Research
University of Warwick
Warwick, United Kingdom2025
Masters in Public Health (MPH) - Public Health
University of Ilorin
Ilorin, Nigeria2009
MBBS - Medicine And Surgery
University of Ilorin
Ilorin, Nigeria2006
Skills
- Understanding of all aspects of trials, site start-up and oversight, study management and site monitoring, study closeout
- Conversant with Electronic Data Capture and Clinical Data Management
- Patient recruitment and retention as well as Informed Consent Process
- Excellent organization and time management with attention to detail and commitment to quality
- In depth knowledge of GCP, CFR, and ICH Guidelines
- Proficiency in clinical trial software and all Microsoft Office applications
- Training and mentoring
- Site operations such as Investigational product management, Standard Operating Procedures , specimen collections and handling and Protocol Review
Certification
- ICH GCP Certification
- CITI HIPAA Research training
- Human Subjects Protection Training
- Data Management for Clinical Research
Accomplishments
- Co-Authored on more than ten individual publications within leading journals, local and international.
Languages
English
Native language
Timeline
Senior Clinical Trial Study Lead
Bioluminux Clinical Research
12.2023 - Current
Clinical Lecturer/ Honorary Hospital Consultant
University Of Medical Sciences
08.2017 - 10.2022
Clinical Lecturer/ Honorary Hospital Consultant
Bowen University/ Bowen University Teaching Hospital
09.2015 - 08.2017
Master of Science - Clinical Research
University of Warwick
Masters in Public Health (MPH) - Public Health
University of Ilorin
MBBS - Medicine And Surgery
University of Ilorin
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