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-time
Work Location: In person
