Skills

  • Project Management
  • clinical research
    8
  • English and Kiswahili

Recommendations

Winnie Lillian

2/15/2025
8

"She is also a good team leader. Ensures that people working under her leadership are okay in their work places for quality service delivery."

Jerry Kelvin

2/13/2025
10

"Gladys is a proficient professional with extensive expertise in clinical trials, regulatory affairs, manuscript writing and phlebotomy procedures. Her in-depth knowledge of clinical research processes is complemented by her ability to navigate complex regulatory frameworks, ensuring compliance with ethical and legal standards for clinical trials. She excels in managing study protocols, preparing and submitting regulatory dossiers and maintaining adherence to Good Clinical Practice (GCP) guidelines. Gladys is also skilled in manuscript writing, adept at synthesizing clinical data into well-structured, high-quality scientific papers, contributing to impactful dissemination of research findings. Her hands-on experience with phlebotomy procedures further highlights her versatility, as she ensures precision and care in sample collection and processing.
These combined skills position Gladys as a reliable and detail-oriented professional, capable of leading and supporting projects in clinical trial management and regulatory affairs with exceptional efficiency."

2 recommendations in total
See all recommendations

Related persons

Vianney AgengoSoftware development, ICT , IT
Jerry Kelvinclinical research

Winnie Lillian

2/15/2025
8

"She is also a good team leader. Ensures that people working under her leadership are okay in their work places for quality service delivery."

Jerry Kelvin

2/13/2025
10

"Gladys is a proficient professional with extensive expertise in clinical trials, regulatory affairs, manuscript writing and phlebotomy procedures. Her in-depth knowledge of clinical research processes is complemented by her ability to navigate complex regulatory frameworks, ensuring compliance with ethical and legal standards for clinical trials. She excels in managing study protocols, preparing and submitting regulatory dossiers and maintaining adherence to Good Clinical Practice (GCP) guidelines. Gladys is also skilled in manuscript writing, adept at synthesizing clinical data into well-structured, high-quality scientific papers, contributing to impactful dissemination of research findings. Her hands-on experience with phlebotomy procedures further highlights her versatility, as she ensures precision and care in sample collection and processing.
These combined skills position Gladys as a reliable and detail-oriented professional, capable of leading and supporting projects in clinical trial management and regulatory affairs with exceptional efficiency."

2 recommendations in total
See all recommendations