At a Glance
- Tasks: Lead clinical research operations and ensure efficient delivery of studies.
- Company: Join a leading organisation in clinical research with a focus on innovation.
- Benefits: Competitive salary, professional development, and a chance to make an impact.
- Other info: Opportunity to lead teams and drive operational transformation.
- Why this job: Drive successful study execution and enhance research capabilities in a dynamic environment.
- Qualifications: Bachelor's degree and 10-12 years in clinical research or project management.
The predicted salary is between 60000 - 80000 £ per year.
What you'll be doing:
- Lead and oversee Clinical Research Unit (CRU) operations to ensure efficient delivery of clinical studies, operational readiness, and alignment with organisational research priorities.
- Partner internal stakeholders, sponsors, CROs, and cross-functional teams to drive successful study execution, operational planning, and issue resolution across the study lifecycle.
- Provide operational leadership and subject matter expertise on clinical research processes, study feasibility, IRB submissions, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Support protocol reviews, study execution planning, milestone management, feasibility assessments, and operational risk mitigation initiatives.
- Drive consistency and quality in study execution through process optimisation, SOP governance, CAPA implementation, root cause analysis, and continuous improvement initiatives.
- Lead and oversee implementation of high-priority clinical and operational projects to support research capabilities and organisational objectives.
- Ensure compliance with approved protocols, IRB requirements, regulatory frameworks, global policies, and internal SOPs across all research operations.
- Participate in audits, inspections, self-assessments, and quality governance activities to maintain operational and regulatory excellence.
- Oversee operational databases, research systems, equipment lifecycle management, and study-related documentation to support CRU capabilities.
- Lead, mentor, and develop research operations teams while driving performance, collaboration, and workforce capability development.
What we're looking for:
- Bachelor's Degree in Life Sciences/ Nursing/ Pharmacy/ Biomedical Sciences/ Clinical Research/ Healthcare Administration or related studies.
- 10 - 12 years of working experience in clinical research operations, project management, or clinical trial management within healthcare, pharmaceutical, CRO, or research environments.
- Strong knowledge of IRB processes, regulatory requirements, GCP guidelines, clinical trial operations, and research governance frameworks.
- Proven experience managing cross-functional clinical study teams, operational delivery, and stakeholder engagement across complex research programmes.
- Experience in audit readiness, quality management systems, CAPA processes, SOP governance, and operational compliance initiatives.
- Strong analytical, problem-solving, and project management skills with ability to manage multiple high-priority studies and operational initiatives simultaneously.
- Excellent communication, leadership, and stakeholder management skills with confidence engaging sponsors, investigators, CROs, and senior leadership.
- Experience leading teams and driving operational transformation or process improvement initiatives will be highly advantageous.
Senior Project Manager, Clinical Research Operations (1-Year Contract) in Penarth employer: JOBSTUDIO PTE. LTD.
At JobStudio, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. As a Senior Project Manager in Clinical Research Operations, you will benefit from our commitment to employee growth through mentorship and professional development opportunities, all while working in a dynamic environment that prioritises operational excellence and compliance. Join us in making a meaningful impact in the healthcare sector, where your expertise will be valued and your contributions recognised.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Project Manager, Clinical Research Operations (1-Year Contract) in Penarth
✨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 lookout for opportunities. You never know who might have the inside scoop on a role that’s perfect for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP guidelines and IRB processes. We want you to be able to showcase your expertise confidently, so practice answering common questions related to clinical trial management.
✨Tip Number 3
Don’t just apply anywhere; focus on roles that align with your experience in operational leadership and project management. Use our website to find positions that match your skills and interests, making your application stand out!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. It shows your enthusiasm for the role and gives you another chance to highlight why you’re the best fit for the team.
We think you need these skills to ace Senior Project Manager, Clinical Research Operations (1-Year Contract) in Penarth
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Senior Project Manager role. Highlight your experience in clinical research operations and project management, focusing on relevant skills that match the job description.
Showcase Your Achievements:Don’t just list your responsibilities; showcase your achievements! Use specific examples of how you've driven successful study execution or improved processes in previous roles to stand out.
Be Clear and Concise:Keep your application clear and concise. Use straightforward language and bullet points where possible to make it easy for us to see your qualifications at a glance.
Apply Through Our Website:Remember to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. We can’t wait to hear from you!
How to prepare for a job interview at JOBSTUDIO PTE. LTD.
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical research operations, GCP guidelines, and IRB processes. Familiarise yourself with the specific requirements mentioned in the job description, as this will show that you're not just interested in the role but also understand what it entails.
✨Showcase Your Leadership Skills
Prepare examples from your past experiences where you've successfully led teams or projects. Highlight how you managed cross-functional teams and resolved issues during the study lifecycle. This will demonstrate your capability to drive operational excellence and mentor others.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving skills and ability to handle operational challenges. Think of scenarios where you had to implement CAPA processes or manage audits, and be ready to discuss how you approached these situations and what the outcomes were.
✨Engage with Stakeholders
Since stakeholder engagement is key in this role, prepare to discuss how you've effectively communicated with sponsors, CROs, and internal teams. Show that you can build relationships and drive collaboration, which is crucial for successful study execution.
