Job Summary
The Clinical Research Assistant plays a vital role in the coordination of patient appointments, the collection and meticulous recording of research data, and the support of various clinical procedures, including ECGs and visual acuity assessments. This position is fundamental in ensuring adherence to ICH-GCP standards and following IRB-approved protocols, thereby maintaining the integrity of clinical research operations.
Responsibilities
- Facilitate and coordinate patient visits for clinical trials.
- Collect and systematically record study-related data.
- Assist in clinical procedures, specifically ECGs and visual acuity testing.
- Maintain precise documentation to support compliance with regulatory guidelines.
- Ensure adherence to ICH-GCP guidelines as well as IRB-approved research protocols.
Qualifications
- Possession of a bachelor’s degree or a minimum of 4 years of relevant experience in the field of ophthalmology.
- Strong verbal and written communication skills.
- Proficiency in using computers and electronic data capture systems.
- Ability to manage multiple tasks in a fast-paced clinical setting.
