At a Glance
- Tasks: Support clinical trials and ensure smooth operations while safeguarding participant well-being.
- Company: Join IQVIA, a leader in clinical research with a focus on innovation.
- Benefits: Part-time hours, flexible work environment, and valuable experience in healthcare.
- Other info: Great opportunity for career growth in the healthcare sector.
- Why this job: Make a real difference in patient care while gaining hands-on research experience.
- Qualifications: BS/BA in life sciences or relevant experience; strong IT and interpersonal skills.
The predicted salary is between 24300 - 29700 £ per year.
Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company? If so, come and join us - IQVIA are looking for a Clinical Research Coordinator. This part-time (24 hours) role is to support a site in Belfast in conducting a clinical trial in the field of respiratory.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
Day to day responsibilities will include:
- Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator.
- Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns.
- Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents.
- Plan and coordinate logistical activity for study procedures according to the study protocol.
- Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues.
- Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness.
- Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol.
- Correct custody of study drug according to site standard operating procedures.
- Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
We are looking for candidates with the following skills and experience:
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession.
- Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules.
- Basic knowledge of medical terminology.
- Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word.
- Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients.
- Good organizational skills with the ability to pay close attention to detail.
Clinical Research Coordinator employer: IQVIA, Inc.
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. Our commitment to employee growth is evident through continuous learning opportunities and the chance to work with cutting-edge technology in the heart of the healthcare industry. Join us in a role that not only challenges you but also allows you to make a meaningful impact on global health outcomes.
