Senior Clinical Research Associate – Site Management

IQVIA

. Perform site monitoring visits, including selection, initiation, monitoring and close-out visits, in accordance with contracted scope of work and Good Clinical Practice.

Posted 11/4/2026full-timeManchester • United KingdomSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in site monitoring, regulatory compliance, and Good Clinical Practice (GCP) while effectively managing project execution and site relationships. Proficient in tracking study metrics and maintaining documentation to ensure quality and integrity in clinical trials.

Highest-signal resume keywords

On-Site Monitoring ExperienceGood Clinical Practice (GCP)Regulatory Requirements KnowledgeMicrosoft Office ProficiencyOrganizational Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Site MonitoringRegulatory Submissions TrackingData Query GenerationProtocol AdministrationStudy TrainingTrial Master File MaintenanceSite Management DocumentationFinancial ManagementSubject Recruitment PlanningQuality Evaluation

Soft Skills

Written CommunicationVerbal CommunicationProblem-Solving SkillsTime ManagementRelationship Building

Tools & Technologies

Microsoft WordMicrosoft ExcelMicrosoft PowerPointLaptop ComputerIPhoneIPad

Industry Keywords

Clinical ResearchInternational Conference on Harmonization (ICH)Therapeutic KnowledgeClinical Trial AgreementsGood Clinical Practice (GCP)

About the role

Key responsibilities & impact

Perform site monitoring visits, including selection, initiation, monitoring and close-out visits, in accordance with contracted scope of work and Good Clinical Practice.
Work with sites to adapt, drive and track subject recruitment plans in line with project needs.
Administer protocol and related study training to assigned sites and establish regular communication with sites.
Evaluate study-site quality and integrity, escalating quality issues as appropriate.
Track regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data query generation and resolution.
Support the study start-up phase where applicable.
Ensure site documents are available for filing in the Trial Master File and verify Investigator's Site File maintenance.
Create and maintain site-management documentation, monitoring visit findings and action plans, including visit reports and follow-up letters.
Collaborate with study team members to support project execution.
Support development of project subject recruitment plans on a per-site basis where applicable.
Manage site finances according to executed clinical trial agreements and retrieve invoices according to local requirements where applicable.

Requirements

What you’ll need

Bachelor's Degree Degree in scientific discipline or health care preferred. Req
Requires at least 2 years of on-site monitoring experience. Req
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Good therapeutic and protocol knowledge as provided in company training.
Proficiency in Microsoft Word, Excel and PowerPoint.
Ability to use a laptop computer, iPhone and iPad where applicable.
Written and verbal communication skills including good command of English language.
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
This role is not eligible for UK visa sponsorship.