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- Tasks: Lead global clinical trials, manage timelines, budgets, and ensure high-quality outcomes.
- Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
- Benefits: Competitive salary, flexible work options, and opportunities for professional growth.
- Other info: Dynamic team environment with a focus on collaboration and innovation.
- Why this job: Make a real impact on patient health through innovative medical treatments.
- Qualifications: Degree in science, 4+ years in biopharma, and strong leadership skills.
The predicted salary is between 55000 - 65000 £ per year.
The Clinical Project Manager provides input to the overall operational trial(s) implementation, manages trial(s) timelines, budget, feasibility, country identification and sites selection, enhanced patient recruitment, and functions as the primary liaison for internal stakeholders and vendors.
- Accountable to deliver Trial(s) on time, within budget, and with highest achievable quality.
- Assist in the review, development and/or writing of clinical trial documents and manuals, including but not limited to Protocol, Case Report Forms, informed consent forms, Clinical Study Report and other regulatory documents.
- Lead the evaluation and selection of investigative sites; responsible for feasibility.
- Select, coordinate and monitor activities of vendors Review of monitoring reports and conduct co-monitoring visits, as needed.
- Develop and manage trial(s) timelines, budget and priorities.
- Participate in data review and discrepancy resolution.
- Ensure set up and maintain all systems in order to plan and implement trial(s) and track progress.
- Generate reports to update management on conduct of trial.
- Ensure appropriate clinical trial supply plans are implemented and managed.
- Develop recruitment plans, risk-mitigation plan, monitor, and implement contingencies as required.
- Participate in monitoring study safety.
- Review key study quality metrics (e.g., eligibility, primary endpoint data, etc.) and determine appropriate action in conjunction with study team.
- Perform initial review of CRO and other third party study vendor invoices to ensure that work is performed in accordance with scope of work.
- Assist with CRA and third party vendor training on protocols and practices.
- Lead the multi-disciplinary trials teams; include the study team meetings.
- Function as the primary contact for trial(s) between Drug Development and other departments.
- Assume responsibility to participate as a member of working groups and perform special projects, as assigned.
- Ensure adherence to Good Clinical Practice and all applicable local and international regulations.
Qualifications:
- BS/BA degree or a relevant degree with strong emphasis on science.
- Minimum of 4 years of experience in the biopharmaceutical industry or other relevant clinical research experience in the conduct and management of multinational clinical trials.
- Minimum of 3 years leading Global trials.
- Must have working knowledge of ICH Good Clinical Practices and other relevant regulatory/health authority experience.
- Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously.
- Demonstrate leadership and problem solving skills.
- Experience in executing a wide range of clinical trial activities (from initiation to clinical study report).
- Used to work in a multidisciplinary setting, strong cooperative team player, ability to be flexible and adapt to a changing environment.
- Good planning, prioritization, problem solving and organizational skills; strong customer-orientation, used to work independently.
- Strong communication skills, used to communicate with a broad range of stakeholders and to build strong positive relationships.
Global Clinical Project Manager - Sponsor Dedicated employer: IQVIA LLC
Contact Detail:
IQVIA LLC Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Clinical Project Manager - Sponsor Dedicated
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. The more people you know, the better your chances of landing that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and role thoroughly. Understand their projects and values, and think about how your experience aligns with their needs. This will help you stand out as a candidate who truly gets what they’re about.
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your answers and boost your confidence. The more comfortable you are speaking about your experience, the better you’ll perform in the real deal.
✨Tip Number 4
Don’t forget to follow up after interviews! A quick thank-you email can go a long way in showing your appreciation and keeping you top of mind. Plus, it’s a great opportunity to reiterate your enthusiasm for the role.
We think you need these skills to ace Global Clinical Project Manager - Sponsor Dedicated
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences that match the Global Clinical Project Manager role. Highlight your experience in managing clinical trials, timelines, and budgets to show us you’re the right fit!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you're passionate about clinical research and how your background aligns with our mission. Be genuine and let your personality come through.
Showcase Your Leadership Skills: Since this role involves leading multi-disciplinary teams, make sure to highlight any relevant leadership experiences. Share examples of how you've successfully managed projects or teams in the past to demonstrate your capability.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy and ensures your application goes straight to the right people. Don’t miss out on this opportunity!
How to prepare for a job interview at IQVIA LLC
✨Know Your Trials
Before the interview, brush up on your knowledge of clinical trials and the specific processes involved. Be ready to discuss your experience with trial timelines, budgets, and patient recruitment strategies. This will show that you understand the role and can hit the ground running.
✨Showcase Your Leadership Skills
As a Global Clinical Project Manager, you'll need to demonstrate strong leadership abilities. Prepare examples from your past experiences where you've successfully led teams or managed multiple priorities. Highlight how you resolved conflicts or overcame challenges in a multidisciplinary setting.
✨Familiarise Yourself with Regulations
Make sure you're well-versed in ICH Good Clinical Practices and any relevant local and international regulations. During the interview, be prepared to discuss how you've applied these guidelines in your previous roles, as this will showcase your compliance knowledge and commitment to quality.
✨Build Rapport with Stakeholders
Communication is key in this role. Think of ways you've effectively built relationships with internal stakeholders and vendors in the past. Be ready to share specific examples of how you’ve navigated complex communications and ensured everyone was aligned on project goals.