Clinical Research Internship

12 hours ago

Houston, Texas, United States Spring Clinical Research Full time

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

Pay: $50.00 per week

Work Location: In person

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