Jonathan Rodriguez-Cabo Mercado
Central Monitoring Lead
Ciudad de México,CMX
Summary
Dynamic professional with extensive experience at GSK, excelling in clinical trial monitoring and site management. Proven track record in reducing project timelines and enhancing operational efficiencies through innovative technologies. Strong adaptive thinking and risk management skills, consistently delivering high-quality results and fostering effective communication among cross-functional teams.
Overview
17
17
years of professional experience
3
3
Languages
Work History
Central Monitoring Lead
GSK
04.2021 - Current
- Reduced project timelines by effectively prioritizing and delegating central monitoring tasks.
- Implemented innovative technologies within central monitoring workflows, driving operational efficiencies.
- Streamlined workflow processes for increased efficiency in central monitoring tasks.
- Conducted thorough site assessments to identify potential risks and develop appropriate mitigation strategies.
- Designed custom reports for key stakeholders that highlighted critical metrics related to trial progress.
- Achieved a high level of customer satisfaction through consistent delivery of exceptional service standards in central monitoring activities.
- Facilitated clear communication between stakeholders, ensuring timely resolution of issues and concerns.
- Optimized resource allocation with effective workload management and capacity planning techniques.
- Improved risk management strategies through the development of robust risk assessment tools.
Project Manager
GSK
04.2014 - 04.2021
- Successfully managed multiple projects simultaneously by prioritizing tasks according to urgency, resource availability, and alignment with organizational goals.
- Planned, designed, and scheduled phases for large clinical projects.
- Coordinated cross-functional teams and resolved conflicts, maintaining a positive work environment throughout the project lifecycle.
- Prepared detailed reports on project status for stakeholders, ensuring transparency and alignment with objectives.
- Provided detailed project status updates to stakeholders and executive management.
- Identified plans and resources required to meet project goals and objectives in clinical trials.
- Met project deadlines without sacrificing build quality or workplace safety.
- Coordinated with cross-functional teams to resolve project issues and mitigate risks.
- Managed risk assessments and implemented mitigation strategies to minimize potential issues during clinical trials.
- Monitored project performance to identify areas of improvement and make adjustments.
Sr Clinical Research Associate
GSK
04.2011 - 04.2014
- Conducted initiation, monitoring and closeout visits to verify study procedures, regulatory documents and data completion.
- Implemented electronic data capturing systems to adhere with clinical research guidelines.
- Reviewed participant eligibility and consent documentation to help researchers achieve accurate and meaningful results.
- Guided development of adaptive systems framework that integrated data from multiple sources to augment training and operational performance.
- Generated and upload assay data and communicated results and reports to multi-disciplinary project teams to influence progression in discovery and development.
- Contributed to the development of study protocols, informed consent forms, and case report forms to ensure consistency across clinical trials.
- Followed drug storage procedures to comply with protocols and SOP requirements.
- Conducted independent research to validate efficacy of solutions, assimilate results and prepare written technical reports.
Quality Control Inspector
Schering-Plough
11.2008 - 03.2014
- Inspected incoming and outgoing materials for accuracy and quality.
- Communicated with production team members about quality issues.
- Inspected quality of products, taking note of functionality, appearance and other specifications.
- Improved product quality by conducting thorough inspections and identifying defects in a timely manner.
Education
Specialist - Mathematics And Statistics
Applied Math & Statistics
Mathematics And Applied Systems Institute, UNAM 05.2001 -
Master of Computer Applications - Technology
ESDEN
Madrid, España 05.2001 -
Bachelor of Science - Medicinal And Pharmaceutical Chemistry
Chemistry Faculty, UNAM
Mexico, Mexico 05.2001 -
Skills
Clinical trial monitoring
Affiliations
- Project Management Institute (PMI)
- Society of Clinical Research Associates (SoCRA)
Languages
Spanish
Bilingual or Proficient (C2)
English
Bilingual or Proficient (C2)
Portuguese
Upper intermediate (B2)
Timeline
Central Monitoring Lead
GSK
04.2021 - Current
Project Manager
GSK
04.2014 - 04.2021
Sr Clinical Research Associate
GSK
04.2011 - 04.2014
Quality Control Inspector
Schering-Plough
11.2008 - 03.2014
Specialist - Mathematics And Statistics
Applied Math & Statistics
05.2001 -
Master of Computer Applications - Technology
ESDEN
05.2001 -
Bachelor of Science - Medicinal And Pharmaceutical Chemistry
Chemistry Faculty, UNAM
05.2001 -
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