Clinical Research Coordinator - Bristol

IQVIA Argentina; Bristol; On-site; GBP 25,000 - 35,000; Part time

Job summary

A leading company in clinical research is seeking a part-time Clinical Research Coordinator in Bristol. This role involves supporting clinical trials in the Respiratory field, managing administrative tasks, and ensuring adherence to protocols. Ideal candidates will have a BS/BA in life sciences and relevant clinical experience. Strong interpersonal and organizational skills are essential for success in this pivotal role.

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, data quality checking, and query resolution.
• Coordinate with study monitor on study issues.

Skills

Interpersonal Skills

Organizational Skills

IT Competence

Attention to Detail

Education

BS/BA in Life Sciences

Tools

MS Office

Job description

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.

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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