Amara Kobbah
847 Gardnersville Road
Monrovia, Montserrado
+231 77 845 923
amara.kobbah@email.com
https://www.linkedin.com/in/amarakobbah

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PROFESSIONAL SUMMARY
Detail-oriented and experienced Senior Clinical Data Manager with over 10 years in the pharmaceutical industry, specializing in clinical trials and data management. Proven track record in ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements. Adept at leading cross-functional teams and managing complex data sets to drive successful clinical outcomes.

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PROFESSIONAL EXPERIENCE

Senior Clinical Data Manager
Meridian Pharmaceuticals Solutions - Monrovia, Montserrado
January 2020 - Present
- Lead the data management team in the design, implementation, and maintenance of clinical databases for multiple oncology trials, ensuring data integrity and compliance with regulatory standards.
- Collaborate with clinical research associates and biostatisticians to develop and validate case report forms (CRFs) and data collection tools, enhancing data quality and efficiency.
- Conduct data validation and quality assurance checks, resulting in a 30% reduction in data discrepancies and improved reporting timelines.
- Train and mentor junior data managers and clinical staff on data management processes and software tools, fostering a culture of continuous improvement.
- Oversee the preparation of data listings and reports for regulatory submissions, contributing to successful trial outcomes and timely approvals.

Clinical Data Manager
Nexus Clinical Research Group - Paynesville, Montserrado
June 2015 - December 2019
- Managed data collection and processing for clinical trials in hematology and oncology, ensuring adherence to GCP and internal SOPs.
- Developed and maintained data management plans, including data validation specifications and data cleaning processes, which improved data accuracy by 25%.
- Coordinated with cross-functional teams to ensure timely delivery of clinical data for interim and final analyses.
- Implemented new database design strategies using Oracle Clinical, enhancing data retrieval and reporting capabilities.

Clinical Research Associate
West Africa Clinical Trials Institute - Monrovia, Montserrado
March 2012 - May 2015
- Conducted site monitoring visits to ensure compliance with study protocols and regulatory requirements, resulting in a 15% increase in site performance metrics.
- Assisted in the development of study protocols and informed consent documents, ensuring clarity and compliance with ethical standards.
- Collaborated with data management teams to resolve data queries and discrepancies, improving overall data quality.

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EDUCATION

Master of Science in Clinical Research
University of Monrovia - Monrovia, Montserrado
Graduated: May 2012

Bachelor of Science in Biology
Cuttington University - Suakoko, Bong
Graduated: May 2010

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SKILLS
- Clinical Data Management
- Good Clinical Practice (GCP)
- Data Validation and Quality Assurance
- Database Design (Oracle Clinical, SQL)
- Biostatistics and Statistical Analysis (SAS, R)
- Project Management
- Team Leadership and Training
- Regulatory Compliance
- Documentation and Reporting
- Multilingual: English, French

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CERTIFICATIONS
- Certified Clinical Research Associate (CCRA)
- Good Clinical Practice (GCP) Certification

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LANGUAGES
- English (Fluent)
- French (Fluent)

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PROFESSIONAL AFFILIATIONS
- Member, Association of Clinical Research Professionals (ACRP)
- Member, Society for Clinical Data Management (SCDM)

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HOBBIES
- Volunteering in health awareness programs
- Reading medical journals and literature
- Hiking and outdoor activities