Clinical Research Internship

Job description:Position Overview:The Clinical Research Intern will assist the clinical research team in the planning, execution, and management of clinical trials. This position offers hands-on experience in clinical research and an opportunity to learn about the regulatory and operational aspects of clinical trials.Key Responsibilities:Assist in the preparation and maintenance of study documents, including protocols, informed consent forms, and case report forms.Support the coordination and communication with clinical trial sites, including scheduling meetings and maintaining regular contact.Participate in data entry, data management, and quality control activities to ensure accurate and reliable data collection.Help with the preparation of regulatory submissions and ensure compliance with all regulatory requirements.Conduct literature reviews and summarize findings relevant to ongoing and upcoming clinical trials.Assist in the recruitment and enrollment of study participants, including screening and consenting participants.Monitor and report on study progress, including tracking enrollment and follow-up activities.Prepare and organize study materials, including lab kits, study binders, and other essential documents.Attend and contribute to team meetings, providing updates on assigned tasks and projects.Perform other duties as assigned to support the clinical research team.Qualifications:Currently enrolled in or recently graduated from a degree program in a related field (e.g., life sciences, public health, nursing, medicine).Strong interest in clinical research and a desire to pursue a career in the field.Excellent organizational and time-management skills with the ability to manage multiple tasks simultaneously.Strong attention to detail and a commitment to producing high-quality work.Effective communication skills, both written and verbal.Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).Ability to work collaboratively in a team environment as well as independently.Basic understanding of clinical research principles, Good Clinical Practice (GCP), and regulatory requirements (preferred).Benefits:Gain practical experience in clinical research and exposure to various aspects of clinical trial management.Opportunity to work with a team of experienced professionals in a supportive and collaborative environment.Mentorship and guidance from senior staff members.Potential for future career opportunities within the organization.Job Types: Full-time, Part-timeWork Location: In person