• Proficient in medical terminology, clinical trial processes, regulatory requirements, and healthcare industry standards.
• Skilled in managing large volumes of clinical data with a focus on accuracy, integrity, and confidentiality.
• Experienced in implementing quality assurance processes to ensure compliance with regulatory standards and client specifications.
• Strong communicator with internal teams, clients, and healthcare professionals.
• Proven problem-solving abilities to identify issues, analyze root causes, and implement solutions for seamless clinical operations.
• Detail-oriented in documenting and reporting clinical data and processes with precision.
• Familiar with electronic data systems, and relevant software tools.
• Skilled in building and maintaining client relationships, understanding their needs, and ensuring satisfaction.
• Collaborative team player effective in multidisciplinary environments involving researchers, clinicians, data managers, and regulatory affairs specialists.
• Adaptive and flexible in accommodating changes in project scope, timelines, and regulatory requirements.
