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For Companies At a Glance
- Tasks: Lead complex clinical trials and manage global project teams to drive impactful research.
- Company: Join a forward-thinking company dedicated to inclusion and human progress.
- Benefits: Opportunities for growth, competitive salary, and a culture that values diversity.
- Other info: Dynamic environment with a focus on innovation and collaboration.
- Why this job: Make a real difference in healthcare while developing your leadership skills.
- Qualifications: Advanced degree preferred with extensive experience in clinical trial management.
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 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
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We can’t stress enough how important it is to build relationships that could lead to job opportunities.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Understand their clinical trial strategies and be ready to discuss how your experience aligns with their goals. We want you to shine and show them why you’re the perfect fit!
✨Tip Number 3
Practice your pitch! You should be able to clearly articulate your experience and how it relates to the role of Director, Clinical Trial Lead. We recommend rehearsing with a friend or mentor to get comfortable with your delivery.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search. Let’s get you that dream role!
We think you need these skills to ace Director, Clinical Trial Lead (all genders) 1
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the role of Director, Clinical Trial Lead. Highlight your project management experience and any relevant therapeutic areas you've worked in to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share specific examples of how you've led complex studies and managed teams effectively.
Showcase Your Leadership Skills: We want to see your leadership style! In your application, mention instances where you've influenced stakeholders or created a positive working environment. This will help us understand how you can contribute to our team culture.
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at StudySmarter!
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 Phase III studies and be ready to discuss how you've successfully managed complex projects in the past.
✨Showcase Your Leadership Skills
Prepare examples that highlight your leadership competencies and how you've influenced teams in a matrix organisation. Think about times when you've motivated stakeholders or created a positive working climate, as these are key aspects of the role.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving abilities and creativity. Prepare to discuss how you would handle operational challenges or mitigate risks in a clinical trial setting, showcasing your strategic thinking and decision-making skills.
✨Communicate Clearly and Confidently
Effective communication is crucial for this role. Practice articulating your thoughts clearly, both verbally and in writing. Be prepared to provide updates and reports, as well as respond to any questions about your previous experiences and how they align with the company's goals.