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- Tasks: Lead and support key clinical study activities with a focus on quality and compliance.
- Company: Join a global team in the dynamic field of clinical research.
- Benefits: Competitive salary, professional development, and opportunities for growth.
- Other info: Work in a collaborative environment with a focus on innovation and excellence.
- Why this job: Make a real impact in healthcare by ensuring successful clinical trials.
- Qualifications: Experience in clinical research and strong understanding of trial operations required.
The predicted salary is between 45000 - 60000 £ per year.
We are hiring a Senior Study Specialist (SS) to join a Global Study Operations team. In this role, you will support and/or lead key clinical study activities including site oversight, vendor management, TMF maintenance, and cross-functional study execution. You will work with increasing independence to ensure study quality, timelines, compliance, and budget adherence.
Key Responsibilities
- Support study setup, documentation, and feasibility/site selection activities
- Oversee CRO deliverables including IRB/EC submissions and approvals
- Manage essential study documents and TMF compliance
- Support investigator training, meetings, and ClinicalTrials.gov updates
- Coordinate vendor oversight, budgets, and clinical trial insurance
- Contribute to risk identification and cross-functional study meetings
Requirements
- BA/BS (life sciences, nursing, health-related field preferred) or equivalent experience
- Clinical research/pharma/biotech experience required
- Experience with CRO/vendor oversight and budget/SOW management
- Strong understanding of clinical trial operations and compliance
If this sounds like a fit, apply now.
Sr Study Operations Specialist employer: Skills Alliance
Contact Detail:
Skills Alliance Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Sr Study Operations Specialist
✨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 a Senior Study Operations Specialist 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 trial operations and compliance. We recommend practising common interview questions related to site oversight and vendor management, so you can showcase your expertise confidently.
✨Tip Number 3
Don’t forget to highlight your experience with TMF maintenance and CRO oversight during interviews. We want to see how you can contribute to study quality and timelines, so be ready to share specific examples from your past roles.
✨Tip Number 4
Apply through our website for the best chance at landing that dream job! We make it easy for you to showcase your skills and experience directly to our hiring team, so don’t miss out on this opportunity.
We think you need these skills to ace Sr Study Operations Specialist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research and study operations. We want to see how your background aligns with the key responsibilities mentioned in the job description.
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're the perfect fit for the Senior Study Operations Specialist role. Share specific examples of your past experiences that demonstrate your skills in vendor management and compliance.
Showcase Your Team Spirit: Since this role involves cross-functional collaboration, let us know about your teamwork experiences. Highlight any instances where you successfully worked with diverse teams to achieve study goals.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role without any hiccups!
How to prepare for a job interview at Skills Alliance
✨Know Your Stuff
Make sure you brush up on clinical trial operations and compliance. Familiarise yourself with the key responsibilities listed in the job description, especially around site oversight and vendor management. This will help you speak confidently about your relevant experience.
✨Showcase Your Experience
Prepare specific examples from your past roles that demonstrate your ability to manage essential study documents and TMF compliance. Highlight any experience you have with CRO oversight and budget management, as these are crucial for the role.
✨Ask Smart Questions
Think of insightful questions to ask during the interview. Inquire about the team dynamics, the types of studies they typically handle, or how they measure success in study operations. This shows your genuine interest and helps you assess if the company is the right fit for you.
✨Be Ready to Discuss Challenges
Prepare to talk about challenges you've faced in previous roles, particularly in managing timelines and compliance. Discuss how you identified risks and what strategies you implemented to overcome them. This will demonstrate your problem-solving skills and readiness for the role.