A resolute Individual with over 14 years experience as a Professional Nurse, 5 years experience working in an NGO environment, and 9 years in Primary Health. Self-driven, excellent leadership and management skills. I pay diligence and am a collaborator. As a nurse Advisor, I have been supporting and Mentoring Department of Health facilities not only within the supported districts. I have experience in managing not only Clinical staff but also Students, and the M&E Team involved in the Programme that I have been helping. I have also managed a clinical research study with 15 mobile clinics and 40 clinical staff.
Experienced with coordinating clinical research studies, ensuring compliance with protocols and regulatory standards, and maintaining meticulous records. Utilizes effective communication and organizational skills to facilitate smooth study operations and collaboration among stakeholders. Knowledge of clinical trial management, project coordination, and regulatory adherence.
A clinical research professional prepared to excel in coordinating study activities and ensuring compliance with regulatory standards. Skilled in maintaining meticulous records and collaborating effectively with interdisciplinary teams to drive successful study outcomes. Reliable team player with strong focus on achieving results and adapting to changing study needs.
Professional coordinator with comprehensive experience in managing study protocols and ensuring compliance with regulatory standards. Skilled in data collection, analysis, and reporting, with strong ability to adapt to evolving project needs. Known for fostering team collaboration and consistently achieving project milestones. Reliable and results-driven, with keen focus on maintaining quality and efficiency in all tasks.
Diligent HIV/STI/AYFS/TB coordinator with solid background in managing clinical research studies and coordinating between multiple stakeholders. Proven track record in ensuring adherence to study protocols and regulatory requirements while facilitating smooth operations. Demonstrated skills in project management and effective communication.
Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in study and HIV Prevention and treatment coordination of activities.
Knowledgeable Study coordinator adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues.
Professional with experience in clinical research coordination, equipped to make significant impact in this field. Demonstrated ability to manage clinical trials, ensure compliance with protocols, and maintain accurate documentation. Strong emphasis on team collaboration, reliability, and adaptability to evolving project requirements. Proficient in patient recruitment, data collection, and regulatory submissions, with results-driven approach that ensures successful study outcomes.
Results-driven research professional prepared for challenges of overseeing clinical studies. Proven track record of managing complex projects and ensuring compliance with research protocols. Known for fostering team collaboration and adapting to evolving project needs, while excelling in data management and regulatory adherence.
Experienced with coordinating clinical trials and managing study logistics. Utilizes comprehensive knowledge of research protocols to ensure compliance and accuracy. Track record of fostering effective team collaboration and maintaining precise documentation throughout research process.
Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals.
Pursuing full-time role that presents professional challenges and leverages interpersonal skills, effective time management, and problem-solving expertise.
Study design
Data collection
Pharmacovigilance
Medical writing
Documentation management
Site monitoring
Study progress tracking
IRB submissions
Subject retention strategies
Study closeout
Clinical research
Protocol development
Patient recruitment
Adverse event reporting
Informed consent process
Clinical data management
Ethics committee liaison
Clinical trial administration
Good clinical practice
Research experience
Data analysis
Participant screening
Medication dispensing
Documentation requirements
Research sops understanding
Good clinical practices
Site management
Trial management
Data collection techniques
Specimen handling
Study protocols
Informed consent
Report preparation
Phlebotomy
Meeting coordination
Records maintenance
Schedule coordination
Specimen collections
Database organization
Adverse event tracking
Laboratory results management
Case report management
Study monitoring
Test environment establishment
Dispensing oversight
Trial oversight
Investigator coordination
Participant recruitment
Protocol review
Continuous improvement
Teamwork
Patient education
Teamwork and collaboration
Problem-solving
Time management
Problem-solving abilities
Leadership skills
Multitasking
Multitasking Abilities
Patient care coordination
Excellent communication
Research planning
Decision-making
Scientific writing
Research design
Self motivation
Time management abilities
Safety reporting
Adaptability and flexibility
Critical thinking
Effective communication
Team collaboration
Active listening
Organizational skills
Detailed documentation
Team building