Job Title

Job Description: The Clinical Research Intern will play a pivotal role in the administration and coordination of clinical research protocols for pharmaceutical industries. This position will involve assisting clinical coordinators and unit leaders with various tasks, including organizing study documentation, managing appointments, and recruiting patients for clinical trials. Key Responsibilities: Assist clinical coordinators in maintaining accurate participant records, consent forms, and protocol amendments, ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. Support patient recruitment efforts by identifying potential participants using databases, outreach programs, and collaboration with healthcare providers. Communicate effectively with potential participants to provide detailed information about study protocols, eligibility criteria, and the clinical trial process. Screen participants to ensure they meet the inclusion and exclusion criteria for specific studies. Follow up with participants to confirm their interest and availability for enrollment in clinical trials. Enter patient information, study data, and results into databases with high accuracy and confidentiality, following clinical trial data management protocols. Prepare for audits and assist with monitoring visits by regulatory authorities and sponsors, ensuring all documentation is complete and up-to-date. Coordinate with suppliers and vendors to obtain necessary study materials and track inventory levels. Requirements and Qualifications: Currently enrolled in a health-related program (medicine, nursing, pharmacy, or related field). Familiarity with health-related terminology and concepts. Strong organizational skills with attention to detail. Ability to multitask and manage time efficiently. Effective communication skills, both written and verbal. Proactive and willing to learn about clinical research processes and regulations. Team player with a collaborative mindset.