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For Companies At a Glance
- Tasks: Lead complex clinical trials and manage global project teams to ensure successful execution.
- Company: Join a forward-thinking company dedicated to inclusion and human progress.
- Benefits: Opportunities for growth, competitive salary, and a culture of belonging.
- Other info: Dynamic environment with a focus on creativity and collaboration.
- Why this job: Make a real impact in clinical research while leading innovative projects.
- Qualifications: Advanced degree and extensive experience in clinical trial management required.
The predicted salary is between 80000 - 100000 £ per year.
Your Role
You will manage multiple studies, projects, and work streams with very high complexity, risk, impact and reach, typically Phase III and registrational/pivotal studies in a hybrid‑sourcing or in‑house model. You will lead large‑sized global project teams in a matrix organization, directing, influencing and motivating stakeholders from closely related areas and beyond, creating a positive working climate. You will develop the clinical trial strategy while being accountable for successful project execution and delivery of the clinical operational budget, timelines and quality standards agreed upon by Governance Committees. You will be a core member of the Clinical Operations Team and leader of the Clinical Trial Team, aligning the trial team with organisational goals, the Clinical Operations Team, and the Global Program Strategy Team.
You will filter, prioritise, analyse and validate complex and dynamic information from a diverse range of external and internal sources to respond to operational and organisational challenges in a holistic manner to mitigate risks. You will demonstrate subject‑matter‑expert level understanding of multiple functions and functional processes, while being familiar with and considering the overall company strategy. You will act as a senior advisor and mentor within the team and beyond, serving as a best‑practice resource within your discipline or across technical functional teams or projects. You will ensure all study‑management activities are completed in accordance with SOPs/WIs and local regulatory guidance including ICH‑GCP, including audit leadership and interview responses. You will contribute to non‑study‑related initiatives in addition to study assignments and provide reports to senior management, including updates and timelines, independently. You will demonstrate a high level of creativity and innovation to support projects from a strategic perspective, able to predict outcomes and drive toward goal achievement.
Who you are
- Advanced degree desirable (MPH, MS, MA, MBA, PharmD); PM certification desirable.
- At least 12 years in clinical research in a CRO or Pharmaceutical/Biotechnology Industry environment with at least 10 years of in‑depth knowledge and experience in clinical trial management including managerial responsibility.
- Expert experience in multiple Therapeutic Areas.
- Requires extensive professional experience in relevant disciplines and substantial project management experience, with strong market and competitor knowledge.
- Expert experience in all aspects of clinical study planning and startup (including budget and resource planning), and in executing the complete range of clinical study activities from start‑up through final study report.
- Strong leadership competencies and influencing skills.
- Effective oral and written communication skills.
- Proven ability to foster partnerships across projects and multidisciplinary teams.
What we offer
We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress.
Director, Clinical Trial Lead (all genders) 1 in London employer: Merck Group
Contact Detail:
Merck Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Director, Clinical Trial Lead (all genders) 1 in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. We recommend practising common interview questions and tailoring your answers to highlight your experience in clinical trial management. Show them you’re the perfect fit for their team!
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. We suggest mentioning something specific from your conversation to show you were engaged and genuinely interested.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you. Plus, applying directly can sometimes give you an edge over other candidates. Let’s get you that job!
We think you need these skills to ace Director, Clinical Trial Lead (all genders) 1 in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences mentioned in the job description. Highlight your clinical trial management experience and any leadership roles you've held, as this will show us you're a great fit for the Director role.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical trials and how your background aligns with our goals. Don’t forget to mention any innovative strategies you've implemented in past projects.
Showcase Your Leadership Skills: Since this role involves leading large global project teams, be sure to highlight your leadership competencies. Share examples of how you've motivated teams and influenced stakeholders in previous roles to demonstrate your ability to create a positive working climate.
Apply Through Our Website: We encourage you to apply directly through our website. This ensures your application gets to the right people quickly and allows us to keep track of all applicants efficiently. Plus, it’s super easy!
How to prepare for a job interview at Merck Group
✨Know Your Stuff
Make sure you have a solid understanding of clinical trial management and the specific therapeutic areas relevant to the role. Brush up on your knowledge of ICH-GCP guidelines and be ready to discuss how you've applied these in past projects.
✨Showcase Your Leadership Skills
Prepare examples that highlight your leadership competencies and how you've successfully influenced and motivated teams in a matrix organisation. Think about times when you’ve navigated complex project challenges and how you fostered collaboration across multidisciplinary teams.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving abilities. Prepare to discuss how you would handle operational challenges or mitigate risks in a clinical trial setting. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Align with Company Values
Research the company’s culture and values, especially their commitment to inclusion and growth. Be prepared to discuss how your personal values align with theirs and how you can contribute to building a positive working climate within the team.