Clinical Research Intern

Description The Clinical Research Intern will assist in the administration and coordination of clinical research protocols for the pharmaceutical industry, ranging from phases I to IV. The intern will primarily provide support to clinical coordinators and unit leaders, performing a variety of administrative tasks related to the planning, organization, and execution of clinical trials. The role will also involve actively contributing to patient recruitment efforts, managing appointments, and other operational tasks necessary for the successful conduct of clinical studies. Responsibilities Assist clinical coordinators and unit leaders in organizing, maintaining, and updating study documentation, including participant records, consent forms, and protocol amendments. Ensure all trial documentation is appropriately filed and complies with Good Clinical Practice (GCP) guidelines and regulatory requirements. Support recruitment campaigns by identifying potential patients for clinical studies, using databases, outreach programs, and collaboration with healthcare providers. Communicate with potential participants, providing detailed information about study protocols, eligibility criteria, and the clinical trial process. Assist in the screening of 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 a high degree of accuracy and confidentiality, following clinical trial data management protocols. Support audit preparation and assist with monitoring visits by regulatory authorities and sponsors by ensuring all documentation is complete and up to date. Coordinate with suppliers and vendors to ensure timely delivery of necessary study materials and assist in tracking inventory levels. General knowledge/competencies 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. Requirements Education/skills Currently enrolled in a health-related program (medicine, nursing, pharmacy, or related field). Basic knowledge of clinical research or a strong interest in learning about clinical trials. Proficient in Microsoft Office Suite (Word, Excel, PowerPoint). Experience with database management or administrative software is a plus. Experience No prior work experience required, though any exposure to clinical research, healthcare settings, or administrative tasks in a health-related context would be an advantage Please add your resume when apply. Thank you!

Location: Monterrey, MX

Posted Date: 6/15/2025