Clinical Research Coordinator

JR United Kingdom; Bristol; On-site; GBP 25,000 - 35,000; Part time

Job summary

A leading company in Clinical Research is seeking a Clinical Research Coordinator for a part-time role in Bristol. This position involves supporting clinical trials in the Respiratory field, ensuring smooth operations, and assisting with patient data collection. Ideal candidates will have a background in life sciences and relevant clinical experience. Strong organizational and interpersonal skills are essential.

Qualifications

• Relevant work experience in a clinical environment or medical setting.
• Basic knowledge of clinical trials and medical terminology.

Responsibilities

• Support clinical research studies and maintain a safe study environment.
• Assist with data entry, quality checking, and query resolution.
• Coordinate with the study monitor on study issues.

Skills

Interpersonal Skills

Organizational Skills

IT Competence

Medical Terminology

Education

BS/BA in Life Sciences

Tools

MS Office

Job description

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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 (15 hours) role, is planned for 6 months and is to support the site in Bristol 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 client
• Good organizational skills with the ability to pay close attention to detail.