Senior Clinical Coordinator

IQVIA; Manchester; On-site; GBP 32,000 - 45,000; Full time

Benefits offered by this job

High autonomy

Global exposure

Variety of therapeutic areas

Collaborative team environment

In-house technology access

Career development opportunities

Work-Life Balance

Job summary

IQVIA is seeking a Senior Clinical Coordinator for the Medicines Evaluation Unit (MEU) in a site-based role. You will set up and coordinate clinical studies, manage timelines and enrolment, and work with CRAs and administration to ensure data integrity and regulatory compliance.

Join a large multidisciplinary team and contribute to study initiation, monitoring, and closeout while delivering high-quality trial operations and effective sponsor communication.

Qualifications

• 2 years of clinical or medical setting experience.
• Strong English language skills.
• Proficient in MS Windows and Office applications (Outlook, Word).
• Excellent interpersonal and customer service skills.
• Attention to detail and ability to work with cross-functional teams.

Responsibilities

• Coordinate site activation through close-out for clinical studies.
• Monitor timelines, performance, and enrolment progress.
• Collaborate with CRAs and Clinical Administration for data and documentation.
• Lead root cause analysis of deviations and implement CAPA with data management.
• Maintain real-time updates with sponsor and stakeholders.

Skills

Clinical Research

Communication Skills

MS Office

Data Management

Tools

MS Windows

Outlook

Word

Excel

Job description

Senior Clinical Coordinator Medicines Evaluation Unit (MEU) This role is site based! The Medicines Evaluation Unit (MEU) Ltd, an IQVIA business, is one of the UK’s leading contract research organisations, and a facility where commitment to excellence is paramount. Possessing extensive pharmaceutical, scientific and clinical expertise, allied with fast volunteer recruitment, both healthy and patient, within a state-of-the-art hospital based research facility, enables the MEU to offer clients positive clinical trial solutions. Join us on our exciting journey!

Job Overview:

Responsible for the set-up and co-ordination of clinical study activities from site activation through to close-out, working with a core study team to ensure effective study delivery. Oversight of study timelines & performance, responding to adjusted strategies as required alongside the Study Recruiter. Liaise with the Clinical Administration team to maintain real-time tracking of subject results & key study data items (e.g. GPR/TOPs), ensuring timely receipt, review & filing of the associated documentation. Collaborate with Clinical Research Associates (CRAs) during site initiation, routine monitoring, and closeout visits to ensure protocol adherence, data integrity, and regulatory compliance. Work collaboratively with a large multidisciplinary clinical team to support study initiation, participant enrolment and randomisation, particularly during the early stages of study delivery. Monitor protocol deviations to ensure timely identification & reporting in compliance with GCP and sponsor requirements. Lead root cause analysis of deviations and collaborate with clinical data management to implement corrective and preventive actions/adjustments to operational practices/staff re-training. Primary liaison with the sponsor company and other relevant internal/external parties during the clinical phase, to provide real-time updates on subject screening & enrolment progress & facilitate timely resolution of enrolment-related queries, eligibility clarifications, and protocol deviations.

Requirements:

2 years of relevant work experience in a clinical or medical setting OR at least 2-3 years of clinical research. Strong written and verbal communication skills including good command of the English language. Good skill in using MS Windows and Office applications such as Outlook and Word. Excellent interpersonal skills. Excellent customer service skills. Ability to pay close attention to detail. Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Join IQVIA to see where your skills can take you

• High level of autonomy.
• Global exposure
• Variety of therapeutic areas
• Collaborative and supportive team environment
• Access to cutting-edge and innovative, in-house technology
• Excellent career development and progression opportunities
• Work-Life Balance, with a strong focus on a positive well-being.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.