Medical Science jobs

Min Qualification: Degree Experience Level: Entry level Experience Length: 1 year Language Requirement: English Working Hours: Full Time - 8 to 5 Applicant Location: Enugu, Nigeria

Responsibilities:

• Assist with clinical trial regulatory document management
• Prepare and maintain electronic regulatory binders
• Enter and review study data in Electronic Data Capture (EDC) systems
• Track study documentation and investigator training records
• Support subject recruitment and pre-screening activities
• Assist with adverse event and protocol deviation documentation
• Review medical records and source documents for completeness
• Prepare reports, logs, trackers, and study-related correspondence
• Schedule investigator meetings and training sessions
• Support quality assurance and compliance activities
• Coordinate with investigators, sponsors, and CROs globally

Requirements:

• Bachelor's degree or higher in: Medicine, Nursing, Pharmacy, Medical Laboratory Science, Public Health, Biological Sciences, and Life Sciences or related field
• Excellent written and spoken English
• Strong computer skills and proficiency with Microsoft Office
• Reliable internet connection and personal computer
• Close attention to detail and ability to meet deadlines
• Ability to work during U.S. business hours

Preferred Qualifications:

• Prior clinical research experience
• GCP certification
• Experience with EDC systems
• Experience with regulatory documentation
• Healthcare or medical records experience

Benefits:

• Comprehensive clinical research training
• Exposure to global clinical trial operations
• Career development opportunities
• Mentorship from experienced investigators and research professionals
• Competitive compensation
• Long-term growth potential within a rapidly expanding research organization