Ibukun Oyekan
Senior Medical Writer
New York
Summary
Versatile Medical Writer proficient in researching, writing and editing diverse content. Works with minimal input to produce engaging, authoritative and error-free work. Autonomous yet communicative with 8-year history of superior performance in remote environments. Skilled professional with core strengths in leadership and goal alignment across teams and external agencies. Proficient at cultivating and retaining key client relationships and business partnerships.
Overview
8
8
years of professional experience
8
8
Certifications
Work History
Clinical Medical Writer
Amgen
03.2022 - Current
- Played instrumental role in creative planning and review sessions, working with resourceful team to elevate quality of content and designs.
- Streamlined workflow processes by implementing efficient project management tools, reducing turnaround times for content delivery.
- Organized material to research and complete writing tasks.
- Followed company policies and editorial guidelines to craft thorough, well-written content.
- Developed engaging articles for online publications, resulting in increased readership and social media shares.
- Enhanced client satisfaction by delivering high-quality written content tailored to specific industries and target audiences.
- Delivered high-impact speeches at conferences or events on behalf of clients or organizations, successfully conveying key messages to attendees.
- Mentored junior writers in developing strong writing skills and adhering to company style guidelines.
- Completed paperwork, recognizing discrepancies and promptly addressing for resolution.
- Participated in team projects, demonstrated ability to work collaboratively and effectively.
- Excellent communication skills, both verbal and written.
Clinical Research Coordinator
World Health Organization, WHO
03.2021 - 04.2022
- Contributed to successful completion of clinical trials by proactively resolving issues, mitigating risks, and meeting deadlines in a fast-paced environment.
- Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
- Directed site initiation visits, establishing key partnerships with local healthcare providers to facilitate successful trial implementation.
- Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
- Collaborated with clinical staff and other healthcare professionals to support clinical trial data accuracy.
- Increased participant retention rates through proactive follow-up efforts and regular engagement activities.
- Maintained compliance with protocols covering patient care and clinical trial operations.
Associate Medical Writer
Pfizer
07.2018 - 02.2021
- Interpreted and synthesized large amounts of scientific data to create compelling messaging, scientific stories and narratives that aligned with client business goals.
- Collaborated with cross-functional teams to ensure accurate representation of scientific data in promotional materials.
- Proofread copy written by colleagues to correct spelling, punctuation, and grammar.
- Facilitated seamless transitions between project stages through effective handover documentation and communication with stakeholders.
- Developed detailed technical documents and user guides for technical products.
- Gained trust and established connections with clients beyond projects to obtain repeat business and widen existing scope and services.
- Observed in-progress operations to identify important steps for technical instructions.
- Engaged with key opinion leaders and clinical trial investigators to author publications.
Senior Medical Writer
Abbott
03.2016 - 06.2018
- Developed training materials for medical writers to enhance their understanding of industry guidelines and best practices, resulting in improved document quality.
- Contributed to successful product approvals by creating persuasive briefing documents and presentations for regulatory authorities.
- Worked closely with software engineers, product managers and other departments to determine accuracy and completeness of technical documentation.
- Applied effective time management techniques to meet tight deadlines.
- Organized and detail-oriented with a strong work ethic.
Education
M.D. - Medicine And Surgery
Obafemi Awolowo University
Nigeria 04.2001 -
Associate of Science - Medical Informatics
Aston University
United Kingdom 04.2001 -
Skills
Team Collaboration
Investigational Product Management
Electronic Data Capture
Patient Recruitment
Good Clinical Practice
Quality Assurance
Biostatistics Knowledge
Data Collection Techniques
Subject Retention Strategies
Critical Thinking
Study Monitoring
Project Management
Protocol Development
Clinical Research Ethics
Efficient Decision Making
Effective Organization Skills
Adverse Event Reporting
Interpersonal Skills
Informed Consent Process
Regulatory Compliance
Time Management
Medical Terminology
Problem Solving
Clinical Knowledge
Clinical Trials
Scientific Writing
Report Analysis
Data Presentation
Data Analysis
Publication Review
Journal Review
Clinical Content Creation
Certification
Certified Clinical Research Professional (CCRP)
Timeline
UC San Diego Science Communication Program
02-2024
Henry Harvin Medical Writing Course
06-2023
Clinical Medical Writer
Amgen
03.2022 - Current
Professional Diploma in Medical Writing (PDMW)
03-2022
Medical Writing for Healthcare Professionals
06-2021
Clinical Research Coordinator
World Health Organization, WHO
03.2021 - 04.2022
Level 3 Certification in Science Writing
03-2020
Certified Medical Writer Course by Technical Writer HQ
08-2019
Associate Medical Writer
Pfizer
07.2018 - 02.2021
Regulatory Affairs Certification - US (RAC)
05-2018
Certified Clinical Research Professional (CCRP)
07-2016
Senior Medical Writer
Abbott
03.2016 - 06.2018
M.D. - Medicine And Surgery
Obafemi Awolowo University
04.2001 -
Associate of Science - Medical Informatics
Aston University
04.2001 -