At a Glance
- Tasks: Lead clinical operations for biotech projects and ensure successful trial execution.
- Company: Join a specialist clinical consulting organisation supporting innovative biotech companies.
- Benefits: Gain exposure to cutting-edge biotech projects and enhance your career in clinical operations.
- Other info: Dynamic role with opportunities for growth in a collaborative environment.
- Why this job: Make a real impact in clinical development and support groundbreaking therapies.
- Qualifications: 7-10 years in clinical operations with strong knowledge of regulations and trial processes.
The predicted salary is between 70000 - 90000 £ per year.
Eblex Group is supporting a specialist clinical consulting organization working with emerging biotech companies to appoint an Associate Director, Clinical Operations. The organisation partners with innovative biotech sponsors to support clinical trial design, study start-up strategy, protocol development, and operational delivery. Their model provides experienced clinical leadership and operational expertise to companies advancing new therapies without the need to build large internal clinical teams.
This role will play a key part in supporting biotech sponsors as they move from clinical planning and protocol development through study start-up and early trial execution.
The Associate Director, Clinical Operations will support the delivery of clinical consulting projects across multiple biotech programs. Working closely with clinical leadership teams and sponsors, you will contribute to the planning and operationalization of clinical trials, with a particular focus on study start-up, operational planning, and vendor strategy.
Key Responsibilities
- Support clinical operations strategy across multiple biotech client programs
- Contribute to clinical trial planning, feasibility assessments, and study start-up activities
- Provide operational input during protocol development to ensure trials are executable
- Support the development of study timelines, operational plans, and resourcing strategies
- Assist biotech sponsors in preparing for trial activation and early study execution
- Support vendor and CRO selection processes and contribute to vendor oversight frameworks
- Ensure clinical activities align with ICH-GCP, FDA regulations, and global regulatory requirements
- Collaborate with cross-functional teams including regulatory, medical, and clinical development
Ideal Profile
- 7–10 years of experience in clinical operations within biotech, pharmaceutical, or CRO environments
- Experience supporting clinical trial start-up and study execution
- Strong understanding of ICH-GCP, FDA regulations, and clinical trial operational requirements
- Experience working within outsourced or hybrid clinical delivery models
- Strong organizational and stakeholder management skills
Why This Role
This position offers the opportunity to work at the front end of clinical development, supporting biotech companies as they translate clinical strategies into operationally executable trials. You will gain exposure to multiple clinical programs, emerging biotech sponsors, and early-stage clinical development strategy.
Associate Director Clinical Operations in London employer: Eblex Group
Eblex Group offers an exceptional opportunity for the Associate Director, Clinical Operations role within a dynamic and innovative rare disease biotech. With a strong emphasis on collaboration and cross-functional teamwork, employees benefit from a supportive work culture that fosters professional growth and development. Located in a fast-paced environment, this position allows for meaningful contributions to clinical development programmes, making it an attractive choice for those seeking impactful and rewarding employment.
StudySmarter Expert Advice🤫
We think this is how you could land Associate Director Clinical Operations in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the biotech and clinical operations space. Attend industry events, webinars, or even local meet-ups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Showcase your expertise! When you get the chance to chat with potential employers, highlight your experience in clinical trial planning and study start-up. Use specific examples from your past roles to demonstrate how you've successfully navigated similar challenges.
✨Tip Number 3
Be proactive! Don’t just wait for job postings to pop up. Reach out directly to companies you admire, like Eblex Group, and express your interest in working with them. A well-timed email can make all the difference!
✨Tip Number 4
Apply through our website! We’ve got a streamlined application process that makes it easy for you to showcase your skills. Plus, it shows you’re genuinely interested in joining our team and helps us get to know you better.
We think you need these skills to ace Associate Director Clinical Operations in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Associate Director, Clinical Operations role. Highlight your experience in clinical operations, especially in biotech or CRO environments, and showcase your understanding of ICH-GCP and FDA regulations.
Craft a Compelling Cover Letter:Your cover letter should tell us why you're the perfect fit for this role. Share specific examples of your past experiences in clinical trial planning and operational delivery, and how they align with our mission at Eblex Group.
Showcase Your Leadership Skills:As an Associate Director, you'll need strong leadership skills. Use your application to demonstrate how you've successfully led teams or projects in the past, particularly in supporting biotech sponsors during study start-up and execution.
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. This way, we can easily track your application and ensure it gets the attention it deserves!
How to prepare for a job interview at Eblex Group
✨Know Your Clinical Operations Inside Out
Make sure you brush up on your knowledge of clinical operations, especially in the biotech sector. Familiarise yourself with ICH-GCP and FDA regulations, as well as the specifics of study start-up and execution. This will help you demonstrate your expertise and show that you're ready to hit the ground running.
✨Showcase Your Project Management Skills
Be prepared to discuss your experience with managing multiple projects simultaneously. Highlight specific examples where you've contributed to clinical trial planning or operational strategies. This will illustrate your organisational skills and ability to handle the complexities of clinical operations.
✨Engage with Cross-Functional Teams
Since collaboration is key in this role, think of examples where you've worked with regulatory, medical, or clinical development teams. Be ready to explain how you navigated different stakeholder needs and contributed to successful outcomes. This shows you can work well in a team-oriented environment.
✨Prepare Questions for Your Interviewers
Have a few thoughtful questions ready to ask your interviewers about their clinical operations strategy and how they support biotech sponsors. This not only shows your interest in the role but also gives you insight into the company's culture and priorities.
