At a Glance
- Tasks: Lead complex clinical trials and manage global project teams to drive impactful research.
- Company: Dynamic pharmaceutical company focused on innovation and inclusion.
- Benefits: Opportunities for growth, competitive salary, and a culture of belonging.
- Other info: Join a team that values creativity and fosters professional development.
- Why this job: Make a real difference in healthcare while leading cutting-edge projects.
- Qualifications: 12+ years in clinical research with strong leadership and communication skills.
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 in London employer: Merck Group
As a Director, Clinical Trial Lead, you will thrive in an inclusive and dynamic work environment that prioritises employee growth and development. Our commitment to fostering a culture of belonging ensures that you will have the opportunity to lead complex global projects while collaborating with diverse teams, all within a supportive framework that values innovation and creativity. Join us to make a meaningful impact in clinical research and enjoy the benefits of a flexible work model that empowers you to achieve your professional goals.
StudySmarter Expert Advice🤫
We think this is how you could land Director, Clinical Trial Lead in London
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups. The more you engage with others, the better your chances of hearing about job openings that might not even be advertised.
✨Showcase Your Expertise
When you get the chance to chat with potential employers, don’t hold back on sharing your knowledge. Talk about your past experiences and how they relate to the role. This is your time to shine and show them why you’re the perfect fit!
✨Follow Up After Interviews
Always send a thank-you email after an interview. It’s a simple way to express your appreciation and reiterate your interest in the position. Plus, it keeps you fresh in their minds as they make their decision.
✨Apply Through Our Website
Don’t forget to check out our website for job openings! Applying directly through us can sometimes give you an edge, as we love seeing candidates who are proactive and genuinely interested in joining our team.
We think you need these skills to ace Director, Clinical Trial Lead in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the specific skills and experiences that align with the Director, Clinical Trial Lead role. Highlight your project management experience and any leadership roles you've held in clinical research.
Craft a Compelling Cover Letter:Use your cover letter to tell us why you're the perfect fit for this position. Share specific examples of how you've successfully managed complex studies and led teams, and don’t forget to show your passion for clinical research!
Showcase Your Achievements:Quantify your successes where possible! Whether it’s improving timelines, managing budgets, or leading successful trials, we want to see the impact you’ve made in your previous roles.
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. 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 successfully managed complex studies 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 resolved conflicts, as these will demonstrate your ability to create a positive working climate.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving skills and ability to handle dynamic information. Prepare to discuss how you've filtered and prioritised complex data in previous roles, and how you mitigated risks while ensuring project delivery.
✨Align with Company Goals
Research the company's mission and values, and think about how your experience aligns with their goals. Be prepared to discuss how you can contribute to non-study-related initiatives and support the overall organisational strategy.
