Clinical Research Coordinator - Belfast

IQVIA; Belfast; On-site; GBP 30,000 - 40,000; Part time

Job summary

A leading clinical research organization in Belfast is seeking a Clinical Research Coordinator to support various clinical trials. The ideal candidate will have two years of clinical trial experience, strong IT skills, and excellent interpersonal abilities. This role offers flexibility and the chance to work within a dynamic team environment, ensuring the smooth execution of clinical studies.

Qualifications

• Two years of experience with clinical trials.
• Basic knowledge of medical terminology.
• Strong IT competence.

Responsibilities

• Support clinical research studies and maintain a safe study environment.
• Safeguard the well-being of subjects and address their concerns.
• Maintain up-to-date study protocols and documents.
• Plan and coordinate logistical activity for study procedures.
• Perform clinical set-up and preparation for the study.
• Assist with data entry and quality checking.
• Assist in study enrollment by recruiting and screening volunteers.
• Correct custody of study drug according to standards.
• Coordinate with study monitor on issues.

Skills

Experience with clinical trials

Knowledge of medical terminology

IT competence in MS Office

Interpersonal skills

Organizational skills

Tools

MS Windows

MS Office (Access, Outlook, Excel, Word)

Job description

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company that offers you an excellent benefits package and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.

This role is to support the site in Belfast in conducting a clinical trial for 24 hours per week.

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:

• Two years of experience with 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 client
• Good organizational skills with the ability to pay close attention to detail.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Learn more at https://jobs.iqvia.com