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Current Experience

  • Clinical Research Associate (CRA)
    Since July 2015
    · Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice. · Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas. · Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. · Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues to Clinical Project Manager (CPM), Clinical Research Specialist (CRS) and/or line manager. · Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. · Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. · Provide assistance to less experienced clinical staff.

Past Experience

  • Regulatory Affairs Executive (Ghana, Liberia, Sierra Leone and The Gambia)
    September 2013 --- July 2015
    • Registration and product license maintenance for GSK Consumer products • Ensuring that Product Variations are submitted when due and implemented • Obtain approval for adverts for OTC products • Responsible for regulatory intelligence by monitoring and keeping in touch with changes in the regulatory environments of all four countries • Ensuring product safety monitoring and pharmacovigilance of all GSK Consumer products by handling of Adverse Event Reports as back up Named Safety Contact for Ghana, Gambia Sierra Lone and Liberia • Maintenance and regular update of all Regulatory Trackers. • Communicate effectively with the commercial team of any new developments or changes to products or processes. • Artwork and Promotional materials vetting and approval. Quality Management System responsibilities on: • Responsible as the Quality Champion • Complaint handling for the company's products and vaccines. • Returned Goods handling. • Ensuring Good Warehousing Practice for all third party warehouse in all four counties • Implementation of Annual Quality Plan activities

  • Regulatory Affairs Associate
    August 2011 --- August 2013
    • Ensuring that Ernest Chemists products comply with the regulations of the Food and Drugs Board (FDB), Ghana Standards Authority (GSA) and the Narcotics Control Board (NCB) • Liaising with, and making presentations to regulatory authorities • Ensure calibrations of all equipments • Ensure the appropriate licensing and legal compliance of products in order to control the safety and efficacy of products. • Negotiating with regulatory authorities for marketing authorization • Developing and writing clear arguments and explanations for new product licenses or registrations and license renewals • Undertake and manage regulatory inspections in all Ernest Chemists facilities • Reviewing company procedures and providing advice on changes to systems • Keeping abreast of international legislation, guidelines to ensure the products meet international markets. • Develop a programmes to ensure staff trained for quality delivery • Liaise with affiliates or suppliers to ensure that all imported food and pharmaceutical products imported are registered and in compliance • Responsible for safe disposal of expired products • Ensure all work complies with GMP GDP, GSP and health and safety requirements in manufacturing, warehouses and outlets/branches. • Respond to questions from regulatory authorities raised during technical reviews and premises inspections • Ensure proper documentation of all regulatory affairs • Implement and review Quality Assurance systems and generate Standard Operating Procedures • Review all regulatory agencies’ compliance materials to guarantee accuracy, timeliness, comprehensiveness, and obedience with regulatory standards • Ensure proper monitoring of controlled, psychotropic and narcotic product of the company

  • Regulatory Officer
    October 2010 --- July 2011
    Ensure the safety, efficacy and quality of food, drugs, cosmetics, medical devices, and biologics


Self Assessment :
Self-disciplineStrategic thinking


Self Assessment :
Clinical trialsRegulatory submissionsRegulatory affairsClinical monitoring
LinkedIn Assessment :
Clinical monitoringClinical Data ManagementGood Laboratory Practice (GLP)Regulatory affairsGMPRegulatory submissionsPharmaceuticsQuality AssuranceRegulatory RequirementsSOPRegulationsTeamworkBiotechnologyGLPPharmaceutical RegulationCTDFDAClinical researchClinical trialsPharmaceutical IndustryComputer ProficiencyFlexibilityStandard Operating Procedure (SOP)PharmacovigilanceGood Clinical Practice (GCP)

Skills and Expertise

Self Assessment :
Monitor a clinical studyTrain on site staffInitiate clinical trials Select sitesremote monitoring


  • Master's Degree in Food Quality Management from Kwame Nkrumah' University of Science and Technology, Kumasi in 2017
  • Bachelor's degree in Applied Biology from University for Development Studies in 2010
  • High School in from St. Thomas Sec. Tech. Sch. Asamankese in 2004
  • Master’s Degree in Drug Discovery- Development & Commercialization from University of California, San Diego in 0

Training and Certification

  • Duolingo French Fluency: Beginner (Estimated) Certification
  • Duolingo French Fluency: Elementary (Estimated) Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency

Area / Region

Accra, Greater Accra Region, Ghana


Driving License
  • No