Job Summary
The role involves providing essential support in clinical research studies by engaging in various tasks including patient screening, enrollment, and monitoring. Responsibilities also comprise obtaining informed consent, scheduling appointments, performing basic assessments, and handling the collection and input of study data. The role is crucial in ensuring compliance with research protocols and maintaining reliable documentation throughout the study process.
Responsibilities
- Assist in screening and enrolling patients for clinical research studies.
- Obtain informed consent from study participants.
- Schedule patient visits and conduct basic assessments.
- Collect and enter data related to the study.
- Maintain accurate study documentation and databases.
- Support the filing of IRB documents and ensure adherence to research protocols.
- Report patient responses to treatment and any adverse effects to the Principal Investigator or designated personnel.
Qualifications
- Experience in a related field ranging from zero to six months, or an equivalent mix of educational background and experience.
- Strong enthusiasm for acquiring knowledge in the field of clinical research.
- Proficient computer skills, particularly in Microsoft Office applications.
- Professional demeanor with effective written and verbal communication abilities.
- Analytical mindset with a keen attention to detail.
Temple University provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
