At a Glance
- Tasks: Lead clinical studies from start to finish, ensuring compliance and effective communication.
- Company: Join IQVIA, a global leader in clinical research and healthcare intelligence.
- Benefits: Enjoy competitive salary, professional development, and a collaborative work environment.
- Other info: Dynamic role with opportunities for growth and learning in a fast-paced industry.
- Why this job: Make a real impact on patient outcomes while advancing your career in clinical research.
- Qualifications: Bachelor's degree in life sciences and project management experience required.
The predicted salary is between 40500 - 49500 £ per year.
The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning, executing, and reporting of assigned studies in compliance with Sponsor processes and regulatory requirements. The CPM is the single point of contact and study team lead for the assigned studies. Responsibilities include:
- Supporting SSO Study Start-up Manager with the development of country/cluster/hub study execution plans and timeline commitments.
- Participating with the recruitment sub-team and supporting the development of innovative solutions for site and patient participation to ensure the delivery of assigned studies on time.
- Proactively identifying risks and opportunities for the assigned studies and developing respective mitigation plans.
- Maintaining a strong knowledge of the study protocol to answer standard operational questions from CRAs, sites and Country/Cluster/Hub personnel.
- Driving the conduct of the study to ensure all study operational aspects are on track.
- Ensuring recruitment targets are met and reviewing enrollment at the site level.
- Overseeing local study team activities to achieve study timelines and quality execution.
- Leading/chairing country/cluster/hub study team meetings and participating in global clinical trial team meetings.
- Maintaining oversight of country/cluster/hub level data management activities.
- Coordinating the study handover process with CRAs and their managers.
- Tracking all study close-out activities and ensuring they are performed in a timely manner.
- Conducting or coordinating training for CRAs to support site readiness to recruit and study execution.
- Evaluating potential challenges/risks in the protocol and operational aspects of the study.
- Accountable for monitoring quality and issue resolution through timely review and approval of study monitoring visit reports.
- Promoting a compliance culture advocating adherence to highest standards and ethical integrity.
- Communicating with CRAs and their managers to ensure issue resolution in a timely manner.
- Supporting inspection readiness and submission preparation for monitoring-related activities.
- Monitoring the status of site budget and contract negotiations.
- Serving as core member of the Global Clinical Trial team as a Country and Hub representative.
Requirements include:
- Bachelor's Degree in Life sciences or related field.
- 5 years of prior relevant experience including > 1 year project management experience.
- Advanced knowledge of job area and broad knowledge of other related job areas.
- Knowledge of clinical trials and applicable clinical research regulatory requirements.
- Strong written and verbal communication skills.
- Strong problem solving and leadership skills.
- Planning, time management and prioritisation skills.
- Attention to detail and accuracy in work.
- Good software and computer skills, including MS Office applications.
- Ability to establish and maintain effective working relationships.
- Good understanding of project financials.
Please note: This role is not eligible for UK visa sponsorship.
Associate Clinical Project Manager Reading employer: Meeveem Limited
Meeveem Limited is an exceptional employer that values its employees by fostering a collaborative and innovative work culture in the heart of Yorkshire. With a strong focus on professional development, employees are encouraged to grow their skills and advance their careers while enjoying competitive benefits and a supportive environment that prioritises work-life balance. Joining Meeveem means being part of a dynamic team dedicated to making a meaningful impact in the cardiovascular and endovascular sectors.
