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Job Description & How to Apply Below
Hampton University Proton Cancer Institute (Hampton Proton) began with a vision. After the instillation of the first proton cancer treatment institute in 1990, rumblings of the therapy's success reached Hampton University president, Dr. William R. Harvey. Upon learning more about the treatment from a Hampton University alumnus, he assembled a team to assess the feasibility of what would become the largest free-standing proton therapy facility in the world.
Hampton Proton provides one of the best healthcare opportunities anywhere in our great nation, and you are a vital member of this important team. How well we accomplish our goals of conquering cancer and saving lives largely depends on your daily contributions, as Hampton Proton's true character is reflected through the manner in which all of our patients are treated. Only your best efforts enable us to continue to achieve excellence in everything we do.
To be considered for Hampton Proton's Internship Program, the following information will be required:
• Completed Hampton Proton Internship Application and Questionnaire.
• Proof of being currently enrolled in a program of study or a recent graduate (within 12 months) from an accredited college/university or technical/vocational institution.
• Proof of good academic standing (unofficial transcripts are acceptable).
• Proof of academic class schedule.
• Recent resume and/or cover letter.
• Applicable course syllabus if academic credit will be applied from your educational institution.
Research Assistant Internship
- Data Collection and Management
- Collect, record, and analyze research data from patients' medical records and patient interviews.
- Ensure accurate documentation of lab results, patient data, and clinical outcomes.
- Assist with data entry into electronic databases, ensuring data integrity and adherence to research protocols.
- Clinical Trial Support
- Assist with patient recruitment, informed consent processes, and follow-up procedures in clinical trials.
- Support the collection of clinical data and biospecimens when applicable, ensuring proper handling, storage, and documentation.
- Help track patient progress in clinical studies and assist with monitoring adverse events or treatment-related side effects.
- Research Protocol Assistance
- Assist with the preparation of research protocols, study designs, and regulatory documentation.
- Review and maintain up-to-date records of study progress and compliance with Institutional Review Board (IRB) protocols and regulatory standards.
- Assist in preparing reports and summaries of research findings for publication or presentation.
- General Administrative Support
- Provide logistical and administrative support to the research team, including scheduling meetings, coordinating study-related activities, and assisting with grant application preparations.
- Prepare and maintain research materials, presentations, and reports for conferences and journal publications.
- Assist with organizing and maintaining research records, reports, and publications in accordance with institutional guidelines.
- Collaboration and Team Support
- Collaborate with other research assistants, research coordinators, Principal Investigators, and clinical staff to ensure seamless integration of data gathering and other clinical research activities.
- Attend research meetings and assist in the planning and coordination of research-related events, including seminars and conferences.
At the completion of an Internship Program, each Student Intern will be required to create a Microsoft PowerPoint presentation that will be performed in a session with other Student Interns where the mentors/supervisors will attend. Topics of discussion should be focused…
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