Sponsor-Focused Clinical Project Manager

Meeveem Limited; Reading; On-site; GBP 65,000 - 90,000; Full time

Job summary

IQVIA in Reading, United Kingdom is seeking an Associate Clinical Project Manager to lead day-to-day planning, execution, and reporting of assigned studies from initiation to close-out. The role serves as the single point of contact for country/cluster/hub teams and requires coordinating with CRAs, trial leads, and global teams to ensure timely delivery.

Key responsibilities include developing execution plans, risk mitigation, feasibility input, study oversight, and training coordination.

Qualifications

• Bachelor's Degree Life sciences or related field Req
• 5 years of prior relevant experience including > 1 years project management experience or equivalent combination of education, training and experience. Req
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i e ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.
• Problem solving - Strong problem solving skills.

Responsibilities

• Supports SSO Study Start-up Manager with the development of country/cluster/hub study execution plans and timeline commitments.
• Participates with the recruitment sub-team and supports the development of innovative solutions for site and patient participation to ensure the delivery of assigned studies on time
• Proactively identifies risks and opportunities for the assigned studies in the country/cluster/hub and develops respective mitigation plans
• Supports study feasibility as requested by the SSO Feasibility Manager by providing input to the study protocol and operational aspects of the study
• Maintains a strong knowledge of the study protocol to answer standard operational questions from CRAs, sites and Country/Cluster/Hub personnel
• Drives the conduct of the study (tracks status, maintains relevant reporting systems, oversees forecasts, progress, and mitigation plans) to ensure all study operational aspects are on track
• Ensures recruitment targets are met and reviews enrollment at the site level including responsibility for obtaining approval from the STUDY LEADER on enrolling above site targets.
• Responsible to set up contingency plan to ensure recruitment targets are achieved in accordance with trial execution plan
• Oversees local study team activities to achieve study timelines and quality execution, (proposing and implementing corrective actions where appropriate), according to Sponsor standards and relevant regulations
• Leads/chairs country/cluster/hub study team meetings, participates in global clinical trial team meetings, as required, and is the single point of contact for the conduct of assigned studies
• Maintains oversight of country/cluster/hub level data management activities, including timely understanding of screen failure reasons and discontinuation rates, review of patient profiles, and proactively identifies data entry issues (on quality and timing) to mitigate queries, proactively identifies query resolution issues
• Coordinates the study handover process with CRAs and their managers to ensure proper documentation and communication, when necessary
• Tracks study budget with appropriate study budget in responsible Country. Ensures timely TCF preparation and submission.
• Processes invoiceable items for site level clinical study activities to allow timely payments
• Serves as core member of the Global Clinical Trial team as a Country and Hub representative responsible for all local level feedback to the global trial execution teams.
• Interfaces with SSU teams to ensure on-time initiation of all sites within geography.
• Interfaces with Country study execution teams, including CRAs and CRA Managers, to ensure on-time recruitment, data delivery, and study close out.

Skills

Project management

English communication

Leadership

Problem solving

Organisation

Cross-functional collaboration

Education

Bachelor's Degree Life sciences or related field

Tools

MS Office

Job description

IQVIA in Reading, United Kingdom is seeking an Associate Clinical Project Manager to lead day-to-day planning, execution, and reporting of assigned studies from initiation to close-out. The role serves as the single point of contact for country/cluster/hub teams and requires coordinating with CRAs, trial leads, and global teams to ensure timely delivery.

Key responsibilities include developing execution plans, risk mitigation, feasibility input, study oversight, and training coordination.