Clinical Trial Protocol Analyst at Mango5

Key Duties and Responsibilities:

• Comply with company policies, procedures, and confidentiality requirements
• Support ADCPRS in clinical research prescreen operations
• Communicate effectively with employees regarding prescreen objectives
• Administer patient prequalification questionnaires and monitor prescreener performance
• Maintain prescreener version histories and documentation
• Demonstrate full knowledge of clinical trial protocols and analyze key inclusion/exclusion criteria
• Perform protocol comparisons within therapeutic areas
• Prepare, manage, and distribute protocol detail materials and prescreen questionnaires
• Obtain all IRB-approved study protocols for start-up activities
• Evaluate concomitant medications, medical indications, and procedures per protocol
• Verify accuracy of collected and entered data
• Perform administrative tasks, including automation and data generation
• Meet deadlines as required by ADCPRS

Education and Experience:

• Matric
• Minimum 1 year of experience in healthcare
• Exceptional attention to detail, organizational skills, and ability to multitask in a fast-paced environment within BPO environment
• Excellent verbal and written communication skills
• Strong customer service skills with internal and external stakeholders
• Clear credit record
• Clear criminal record
• Maintain GCP certification and any other on-the-job required certifications