- Bachelor’s degree in a relevant field (e.g., life sciences, healthcare)
- Previous experience in clinical research coordination or a related role
- Familiarity with regulatory requirements and guidelines for clinical trials
- Strong organizational and multitasking skills
- Excellent attention to detail
- Effective communication and interpersonal skills
- Ability to work well in a team
- Proficiency in Microsoft Office Suite and data management systems
Preferred Qualifications:
- Master’s degree in a relevant field
- Certification in clinical research (e.g., ACRP, SoCRA)
- Experience with electronic data capture (EDC) systems
- Knowledge of Good Clinical Practice (GCP) guidelines
Role Description:
- Participant Recruitment: Engage and recruit participants for clinical trials.
- Data Collection and Analysis: Ensure accurate and thorough data collection and perform preliminary data analysis.
- Regulatory Compliance: Ensure all activities comply with regulatory requirements and guidelines.
- Documentation: Maintain accurate and complete documentation of all research activities.
- Collaboration: Work closely with healthcare professionals and research teams to facilitate the smooth execution of research projects.
Application Process:
To apply for this role, please submit your resume and a cover letter highlighting your relevant experience and qualifications. Our hiring team will review all applications and contact shortlisted candidates for further assessment.