OPS Clinical Research Internship

University of Florida•Gainesville, FL

4d•Onsite

About The Position

The UF Health Cancer Institute is the 72nd NCI designated cancer center and the only one at a public university in the State of Florida. As a matrix cancer center, we span all of the University of Florida's 16 colleges, pulling together a world-class, multi-disciplinary membership of over 350 faculty and 150 staff to address the challenges of the cancer burden faced by the population we serve as we work together to find a cure. As part of our commitment to developing the cancer research workforce, our Clinical Research Internship provides recent college graduates with an interest in exploring and establishing a career in clinical research, healthcare, or public health the opportunity to work closely with and learn from physicians, investigators, study staff, and other partners throughout UFHCI and UF Health as they prepare for future careers in healthcare, public health, and academic research. During this year-long experience, you will be embedded in one of our clinical research units and work alongside our study teams, clinical investigators, and partners in the UF Health system to support ongoing oncology clinical research. You will be provided with personalized mentorship and unique training opportunities developed specifically for this program, engage with the clinical research process under the guidance of staff and faculty experts, and obtain valuable experience to take with you in your future graduate or professional degree programs as you prepare for your future career.

Requirements

Proof of eligibility to graduate and/or a recently awarded Bachelors' degree in one of the basic sciences, health sciences, or similar field with a cumulative GPA of 3.2. Degree must be conferred prior to the beginning of your internship.
Availability for 40 hours per week during normal business hours (8 AM - 5 PM) for the duration of the program.
Bachelor’s Degree in Health Science, Basic Sciences, Public Health, or similar field.
Excellent time management skills and attention to detail.
Demonstrated ability to work independently and interact professionally.
Effective writing and organizational skills.
Proficiency using the Microsoft Office suite.

Nice To Haves

Experience with laboratory processes, including shipping of human samples, processing, and storage.
Knowledge of clinical research processes, medical terminology, and healthcare documentation.
Experience reviewing medical records and abstracting clinical data for research or healthcare documentation.
Highly resourceful team-player, with the ability to also be effective independently, maintain appropriate discretion, and utilize effective writing and organizational skills.
Demonstrated understanding and effective use of emotional intelligence strategies and skills.
Demonstrated ability to manage multiple priorities while interacting professionally with diverse stakeholders.

Responsibilities

Attending study-focused training sessions and developing proficiency in various clinical research activities such as screening, consenting, enrollment and follow up of participants.
Review and transcription of medical and clinical data from a variety of sources related to potential and existing research subjects.
Interacting with participants to obtain data, administer questionnaires and collect specimens.
Learn about principles of Good Clinical Practice, study design, compliance and other research considerations.
Proposing and executing a quality improvement project in collaboration with investigators and study staff.