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- 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: Competitive salary, professional development, and a chance to make a real impact.
- Other info: Dynamic work environment with opportunities for growth and collaboration.
- Why this job: Be at the forefront of innovative medical treatments and improve patient outcomes.
- Qualifications: Bachelor's degree in life sciences and 5 years of relevant experience required.
The predicted salary is between 40000 - 50000 £ 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. The CPM is responsible for assuring aligned communication with Trial Leads and other CTT members, locally with Clinical Research Associates (CRAs), CRA Managers and other key associates on the execution and progress of their studies. The CPM collaborates with various managers in the planning, execution, and delivery of their assigned studies.
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 and develops respective mitigation plans.
- 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 to ensure all study operational aspects are on track.
- Ensures recruitment targets are met and reviews enrollment at the site level.
- Oversees local study team activities to achieve study timelines and quality execution.
- Leads/chairs country/cluster/hub study team meetings and participates in global clinical trial team meetings.
- Maintains oversight of country/cluster/hub level data management activities.
- Coordinates the study handover process with CRAs and their managers.
- Tracks all study close-out activities and ensures they are performed in a timely manner.
- Conducts or coordinates training for CRAs to support site readiness to recruit and study execution.
- Evaluates 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.
- Promotes a compliance culture advocating adherence to highest standards and ethical integrity.
- Acts as the escalation point for issues in monitoring visit reports for the assigned studies.
- Provides feedback about the quality of monitoring activities to relevant managers.
- Supports inspection readiness and submission preparation for monitoring-related activities.
- Monitors the status of site budget and contract negotiations.
- Serves as core member of the Global Clinical Trial team as a Country and Hub representative.
- Interfaces with SSU teams to ensure on-time initiation of all sites within geography.
- Interfaces with Country study execution teams to ensure on-time recruitment, data delivery, and study close out.
Requirements:
- 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 skills.
- Ability to work through others to deliver results.
- 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 - Sponsor Dedicated employer: IQVIA
Contact Detail:
IQVIA Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Clinical Project Manager - Sponsor Dedicated
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the hunt for an Associate Clinical Project Manager role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical trials and project management. Be ready to discuss how you've tackled challenges in past projects and how you can bring that experience to the table at IQVIA.
✨Tip Number 3
Showcase your leadership skills during interviews. Talk about times when you've led a team or managed a project, and highlight how you ensured quality and compliance throughout the process. This will demonstrate that you're the right fit for the CPM role.
✨Tip Number 4
Don't forget to apply through our website! It's the best way to ensure your application gets seen by the right people. Plus, it shows you're serious about joining the IQVIA team and ready to make an impact in clinical research.
We think you need these skills to ace Associate Clinical Project Manager - Sponsor Dedicated
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Associate Clinical Project Manager role. Highlight your project management experience and any relevant clinical trial knowledge to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your background makes you the perfect fit. Keep it concise but impactful!
Showcase Your Communication Skills: Since strong communication is key for this position, make sure your application is clear and well-structured. Use proper grammar and spelling, and don’t hesitate to show off your personality a bit!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!
How to prepare for a job interview at IQVIA
✨Know Your Stuff
Make sure you have a solid understanding of clinical trials and the specific responsibilities of an Associate Clinical Project Manager. Brush up on ICH GCP guidelines and be ready to discuss how you've applied these in your previous roles.
✨Showcase Your Communication Skills
As a CPM, you'll need to communicate effectively with various stakeholders. Prepare examples of how you've successfully led meetings or resolved conflicts in the past. Practise articulating your thoughts clearly and confidently.
✨Be Proactive About Problem-Solving
Think of instances where you've identified risks or challenges in a project and how you addressed them. Be ready to discuss your approach to developing mitigation plans and ensuring study timelines are met.
✨Demonstrate Leadership Qualities
Highlight your experience in leading teams and managing performance. Share specific examples of how you've motivated others and driven results, especially in cross-functional settings. This will show that you're ready to take charge in this role.