ICRS Hiring Clinical Research Coordinator

• 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.

Application Link