Job title : Clinical Trial Protocol Analyst Job Location : Eastern Cape, Deadline : November 10, 2025 Quick Recommended Links 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 Medical / Healthcare jobs
