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For Companies At a Glance
- Tasks: Lead global clinical trials, manage timelines, and ensure project deliverables.
- Company: Join a top 10 global CRO with a strong reputation in life sciences.
- Benefits: Enjoy a competitive salary, annual bonus, stock options, and a strong healthcare package.
- Why this job: Make an impact in life sciences while working in a dynamic and supportive environment.
- Qualifications: Life science degree and 5+ years in clinical trial management required.
- Other info: Hybrid work model: 4 days in office, 1 day from home.
The predicted salary is between 73000 - 97000 £ per year.
Location: London (4 days in office, 1 day from home)
Reporting into: VP of Clinical Operations
Company: Top 10 CRO (4,000-5,000 employees)
Apsida Life Science is exclusively partnering with a leading global CRO that is looking to appoint an Associate Director, Clinical Trial Manager to be based in London. The Associate Director Clinical Trial Manager will act as the project lead for multiservice full service global clinical trials. The position interacts with sponsors and manages the timeline and all project deliverables.
Responsibilities:
- Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
- Serve as primary Sponsor contact for operational project-specific issues and study deliverables
- Maintain in depth knowledge of protocol, therapeutic area, and indication
- Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
- Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
- Develop operational project plans
- Manage risk assessment and execution
- Responsible for management of study vendor
- Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables
We are looking for:
- Life science relevant degree
- Experience working for a CRO
- Experience in either Oncology, Cardiovascular or GI
- 5+ years in a Clinical Trial Manager or Clinical Project Manager position for a full service CRO that is looking to take a step up!
What’s on offer:
- £85,000 - £110,000 per year
- 10% annual bonus
- LTI, stock options
- Strong healthcare package
- Annual grants
- Car allowance, £6,000
If you’re interested in learning more, please reach out to Jamie Salmon from Apsida Life Science.
Associate Director, Clinical Trial Manager employer: Apsida Life Science
Contact Detail:
Apsida Life Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director, Clinical Trial Manager
✨Tip Number 1
Network with professionals in the clinical trial management field, especially those who have experience in CROs. Attend industry events or webinars to connect with potential colleagues and learn more about the company culture at Apsida Life Science.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical trials, particularly in Oncology, Cardiovascular, and GI. This knowledge will not only help you stand out but also demonstrate your commitment to staying updated in the field.
✨Tip Number 3
Prepare to discuss your previous experiences managing clinical trials, focusing on specific challenges you faced and how you overcame them. Highlight your leadership skills and ability to manage cross-functional teams effectively.
✨Tip Number 4
Research Apsida Life Science thoroughly, including their recent projects and company values. Tailoring your conversation to align with their mission can show your genuine interest in the role and the organisation.
We think you need these skills to ace Associate Director, Clinical Trial Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial management, particularly in Oncology, Cardiovascular, or GI. Use specific examples that demonstrate your ability to manage projects and interact with sponsors.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for the role and the life sciences industry. Mention your experience with CROs and how it aligns with the responsibilities of the Associate Director position.
Highlight Leadership Skills: In your application, emphasise your leadership and cross-functional oversight abilities. Provide examples of how you've successfully managed teams and ensured project deliverables in previous roles.
Showcase Regulatory Knowledge: Demonstrate your understanding of ICH/GCP guidelines and other applicable regulations in your application. This will show that you are well-versed in the necessary compliance aspects of clinical trials.
How to prepare for a job interview at Apsida Life Science
✨Know Your Protocols
Familiarise yourself with the specific protocols and therapeutic areas relevant to the role. Being able to discuss these in detail will demonstrate your expertise and commitment to the position.
✨Showcase Your Leadership Skills
As an Associate Director, you'll need to lead teams effectively. Prepare examples of how you've successfully managed projects and teams in the past, highlighting your ability to oversee operations and deliver results.
✨Understand the CRO Landscape
Research the company and its position within the CRO industry. Understanding their services, client base, and recent projects will help you tailor your responses and show genuine interest in the organisation.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and decision-making abilities. Think of scenarios where you've had to manage risks or resolve conflicts, and be ready to discuss your approach and outcomes.
