Senior Clinical Coordinator: Global Impact, Autonomy & Growth

IQVIA Holdings Inc.; Manchester; On-site; GBP 25,000 - 40,000; Full time

Benefits offered by this job

Global exposure

High autonomy

Collaborative team environment

Cutting-edge in-house technology

Excellent career development

Work-Life Balance

Job summary

IQVIA Holdings Inc. is seeking a coordinator to manage study activities from site activation through close-out. You will work with a core team to ensure timely enrolment, data integrity and regulatory adherence, liaising with sponsors and internal teams for real-time updates.

The role emphasizes collaboration across disciplines, ongoing monitoring of protocols and deviations, and ensuring high standards of quality and patient safety in a fast-paced environment.

Qualifications

• 2 years of relevant work experience in a clinical or medical setting or 2–3 years in clinical research.
• Strong written and verbal communication skills with good command of English.
• Proficient use of MS Windows and Office applications (Outlook, Word).
• Excellent interpersonal and customer service skills.
• Ability to pay close attention to detail.
• Ability to build effective working relationships with coworkers, managers and clients.
• Experience within IQVIA MEU or a hospital-based clinical research environment is a plus.

Responsibilities

• Set up and coordinate clinical study activities from site activation to close-out.
• Monitor timelines, performance and respond to adjusted strategies with the study team.
• Liaise with Clinical Administration to track subject results and key data items in real time.
• Collaborate with CRAs during initiation, monitoring and closeout visits to ensure protocol adherence and data integrity.

Skills

Communication skills

Verbal & written English

Attention to detail

Interpersonal skills

Customer service skills

Relationship management

Tools

MS Windows

Outlook

Word

Job description

IQVIA Holdings Inc. is seeking a coordinator to manage study activities from site activation through close-out. You will work with a core team to ensure timely enrolment, data integrity and regulatory adherence, liaising with sponsors and internal teams for real-time updates.

The role emphasizes collaboration across disciplines, ongoing monitoring of protocols and deviations, and ensuring high standards of quality and patient safety in a fast-paced environment.