Job Title
As a Clinical Research Assistant, you will play a vital role in the conduct of an investigator-initiated clinical trial, focusing on the Genetics of Glaucoma Trial. This trial aims to investigate the effectiveness of determining the frequency of eye examinations for glaucoma based on a person's estimated genetic risk.
Key Responsibilities:
* Collaborate with research staff and clinicians to ensure the smooth conduct of the clinical trial, including the consent process and coordination.
* Manage and collate data for participant ocular assessments, such as visual fields, OCT imaging, and intraocular pressure.
* Support clinical procedures and data collection in accordance with trial protocols, receiving comprehensive training.
* Oversee patient scheduling, communication, and accurate data entry.
* Develop strong relationships with patients, optometrists, and healthcare staff to facilitate efficient trial delivery.
Essential Qualifications and Skills:
* A tertiary qualification in Nursing, Orthoptics, or a relevant medically registered discipline.
* Basic knowledge of clinical assessments used in optometry, such as visual fields, intraocular pressure, and ocular imaging.
* Excellent interpersonal skills, including effective communication and the ability to form productive professional relationships.
* Proven ability to build and maintain excellent rapport with diverse patients, ensuring compassionate care and communication.
* Demonstrated proficiency in Microsoft Office Suite.
* A solutions-oriented approach with a commitment to collaborative work and fostering a supportive team environment.
Desirable Qualifications and Skills:
* Understanding of clinical trial processes, ethics, governance, privacy, and ICH-GCP principles.
* Knowledge of clinical genetic risk scores.
* Current GCP certification.
* Ability to utilize project tracking tools and systems related to research trials.