At a Glance
- Tasks: Lead clinical trials and manage a team to ensure exceptional study performance.
- Company: Join Merck, a leader in innovative healthcare solutions committed to diversity and inclusion.
- Benefits: Enjoy flexible hybrid work arrangements and opportunities for professional growth.
- Why this job: Make a real impact in clinical research while nurturing future leaders in a collaborative environment.
- Qualifications: Significant experience in clinical trials and management; a degree in Science or equivalent is required.
- Other info: We value diverse ideas and encourage respectful challenges to foster innovation.
The predicted salary is between 43200 - 72000 £ per year.
As the Therapy Area Head, you will play a pivotal role in overseeing the performance of our clinical trials across multiple therapeutic areas. This is your opportunity to lead a dynamic team and make a significant impact on our clinical research portfolio. You’ll have oversight of the clinical trials across multiple therapeutic areas, managing a portfolio of studies from feasibility through to close-out.
You will lead a team of Clinical Research Managers to ensure exceptional study performance whilst adhering to local regulations, Standard Operating Procedures (SOPs), and ICH Good Clinical Practice (GCP) guidelines. You will play an integral role in our UK&I Leadership team and be instrumental in nurturing talent, fostering a robust pipeline of future leaders. You’ll collaborate closely with local stakeholders such as Global Medical Affairs (GMA), Global Health and Human Services (GHH), Pharmacovigilance (PV), and regulatory bodies, to drive alignment and enhance the capabilities of our clinical research landscape.
What You Will Do:
- Oversee our therapeutic areas within our growing clinical trial portfolio, ensuring successful execution and quality.
- Ensure timelines and key milestones are met while maintaining high standards of quality and compliance with local regulations and ICH GCP.
- Create operational strategies and quality plans for the conduct of all programs and studies in your therapeutic area.
- Provide oversight and line management for the Clinical Research Manager (CRM) team, fostering talent development and retention.
- Work closely with local and regional stakeholders to build relationships with principal investigators and sites.
- Contribute to strategic initiatives across Global Clinical Development and support local strategy development aligned with corporate needs.
- Together with your team, ensure the effective conduct of clinical studies while maintaining regulatory requirements.
- Directly influence our ability to achieve business targets and foster productive collaborations with internal and external partners.
What you will need:
- Significant experience within a pharmaceutical, clinical trial organization in a functional management position.
- CRA, project management and CRM experience.
- Line management experience.
- Bachelor’s degree in Science or equivalent healthcare experience.
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
Therapeutic Area Head (Director) - Clinical Operations employer: Merck Gruppe - MSD Sharp & Dohme
Contact Detail:
Merck Gruppe - MSD Sharp & Dohme Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Therapeutic Area Head (Director) - Clinical Operations
✨Tip Number 1
Network with professionals in the clinical operations field. Attend industry conferences or local meetups to connect with individuals who may have insights into our company and the role of Therapeutic Area Head.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical trials, particularly ICH GCP guidelines. This knowledge will not only help you in interviews but also demonstrate your commitment to maintaining high standards in clinical research.
✨Tip Number 3
Prepare to discuss your leadership style and how you've successfully managed teams in the past. Highlight specific examples where you've nurtured talent and driven team performance, as this is crucial for the role.
✨Tip Number 4
Research our company's clinical trial portfolio and be ready to discuss how your experience aligns with our therapeutic areas. Showing that you understand our work will set you apart from other candidates.
We think you need these skills to ace Therapeutic Area Head (Director) - Clinical Operations
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical operations, project management, and team leadership. Emphasise your familiarity with ICH GCP guidelines and any specific therapeutic areas you have worked in.
Craft a Compelling Cover Letter: In your cover letter, express your passion for clinical research and your vision for leading a team. Mention how your previous experiences align with the responsibilities of the Therapeutic Area Head role and how you can contribute to the company's goals.
Showcase Leadership Skills: Provide examples of how you have successfully managed teams and developed talent in your previous roles. Highlight any initiatives you have led that improved study performance or compliance with regulations.
Highlight Collaborative Experience: Discuss your experience working with various stakeholders, such as principal investigators and regulatory bodies. Illustrate how you have built relationships that enhanced clinical trial outcomes and contributed to strategic initiatives.
How to prepare for a job interview at Merck Gruppe - MSD Sharp & Dohme
✨Showcase Your Leadership Skills
As a Therapeutic Area Head, you'll be leading a team of Clinical Research Managers. Be prepared to discuss your previous leadership experiences, how you've nurtured talent, and your approach to fostering a collaborative environment.
✨Demonstrate Your Knowledge of GCP and Regulations
Since adherence to ICH Good Clinical Practice and local regulations is crucial, brush up on these guidelines. Be ready to provide examples of how you've ensured compliance in past projects and how you would implement these standards in your new role.
✨Prepare for Strategic Discussions
This role involves contributing to strategic initiatives across Global Clinical Development. Think about how you can align local strategies with corporate needs and be ready to share your insights on improving clinical trial execution and quality.
✨Build Relationships with Stakeholders
Collaboration with local and regional stakeholders is key. Prepare to discuss your experience in building relationships with principal investigators and sites, and how you plan to enhance these collaborations in the future.