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Summary of Post
This role is based at the Cardiovascular Research Institute (CVRI Dublin), Mater Private Dublin. The vision for Cardiology at the Mater Private Network includes establishing an academic cardiology department. A fundamental part of this vision is to ensure that excellence in clinic care is supported by and in turn partners with research and education, both nationally and internationally. Research and education can positively impact outcomes for patients, and drive improvements in quality of care.
Specifically, the duties of the post are:
The Clinical Research Assistant will work as part of the research team at the Cardiovascular Research Institute Dublin at the Mater Private Hospital. The Research Assistant will work with the Clinical Research Nurse in the areas of Outcomes Research and Clinical Trials. They will participate in recruitment, data collection & entry, and coordination of study visits, as part of a multidisciplinary team.
Research Responsibilities
* Work within the standard operating procedures and protocols associated with industry and academic clinical research, ensuring all activities are completed to the highest standard in accordance with ICH-GCP and HPRA/EU Directive requirements.
* Support ongoing clinical research projects from participant recruitment through follow-up, identifying problems early and providing regular feedback to the Principal Investigator (PI) and research team.
* Liaise with clinical research associates to resolve queries, assist with monitoring visits, and study close-out activities.
* Ensure patient confidentiality and dignity are always maintained during research activities, in line with GDPR legislation.
* Ensure participants are fully informed about the clinical trial/research project prior to enrollment.
* Schedule and conduct study follow-up visits, including data collection, administering questionnaires, and recording vital signs such as blood pressure.
* Extract required data from patient charts and hospital IT systems, ensuring accuracy and timeliness.
* Process biological samples as required, including coordinating shipments and storage.
* Manage study-related correspondence promptly.
* Prepare documentation for audits as needed.
* Collect and input data into the PCI Outcomes Registry.
* Attend conferences and study days as required.
* Perform additional duties as assigned by the Clinical Research Nurse.
Qualifications (Essential):
* B.Sc. in biological sciences or related area, or equivalent experience.
Knowledge & Experience (Essential):
* Knowledge of research study procedures.
* Excellent interpersonal and communication skills.
* Computer literacy with Microsoft Office.
* Willing to undertake training in clinical assessment techniques and biological sample handling.
Skills & Competencies:
* Effective communication of complex ideas.
* Ability to assist with project planning and meet deadlines.
* Self-motivated team player.
* Proficient in MS Office.
* Detail-oriented with a proactive approach.
* Flexible working hours and environment adaptability.
* Strong customer service skills and confidentiality.
* Enthusiastic and committed to CVRI development.
Note: We encourage all qualified candidates to apply, recognizing that confidence gaps can hinder applications. We look forward to hearing from you.
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