At a Glance
- Tasks: Lead a team to ensure successful execution of clinical trials and maintain compliance.
- Company: Join Galderma, a global leader in clinical research with a collaborative culture.
- Benefits: Hybrid working model, professional development, and the chance to make a real impact.
- Other info: Opportunity for career growth and visibility across local and global teams.
- Why this job: Be a key player in driving operational excellence and improving clinical trial processes.
- Qualifications: 6-8+ years in clinical research and proven leadership skills required.
The predicted salary is between 55000 - 65000 £ per year.
The Clinical Trial Associate Manager plays a key leadership role in ensuring the successful execution of clinical trials by overseeing a team of Clinical Trial Associates (CTAs). This position combines people leadership with operational excellence, driving consistency across clinical trial activities and Trial Master File (TMF) management. You will be responsible for developing talent, ensuring high-quality deliverables, and maintaining compliance with ICH‑GCP, regulatory requirements, and sponsor SOPs. This is a highly collaborative role, working cross‑functionally to support inspection readiness and continuous improvement across the clinical operations function.
Key Responsibilities
- People Leadership & Resource Management
- Lead, mentor, and develop a team of CTAs, fostering a high‑performance and collaborative environment.
- Oversee onboarding, training, performance management, and career development.
- Allocate and balance workloads across multiple clinical trials.
- Act as the primary escalation point for CTA‑related topics.
- Operational Oversight
- Ensure effective CTA support across all assigned clinical trials.
- Oversee the timely and accurate completion of key study deliverables, including:
- Study training trackers
- ADI logs
- Study team rosters
- System access management
- Study and country insurance documentation
- Public registry updates
- Ensure all TMF activities meet sponsor standards and ICH‑GCP requirements.
- Collaborate closely with TMF and Clinical Standards teams to maintain inspection readiness.
- Support internal audits and regulatory inspections.
- Ensure alignment between CRO/vendor documentation and sponsor expectations.
- Monitor quality and consistency across external partners.
- Review performance metrics to identify trends, risks, and improvement opportunities.
- Partner with leadership to drive process optimization and operational excellence.
- Contribute to SOPs, work instructions, and training materials.
Qualifications
- Education
- Bachelor’s degree in Life Sciences or a related field.
- Experience
- 6–8+ years of experience in clinical research (Sponsor and/or CRO environment).
- Proven experience managing and developing global CTA teams.
- Hands‑on experience supporting different study models (e.g., FSP, Hybrid, Phase IV).
- Skills
- Strong knowledge of ICH‑GCP and sponsor‑side clinical operations.
- Demonstrated leadership and stakeholder management skills.
- Excellent organizational and prioritization abilities.
- Preferred Qualifications
- Experience with eTMF systems (e.g., Veeva Vault, TransPerfect).
- Exposure to global clinical trials.
- Project management experience or certification.
What we offer in return
At Galderma, you will have the opportunity to lead regional operations across multiple markets and gain visibility across both local and global teams. You’ll be part of a collaborative, cross‑functional environment with the autonomy to make a real impact on the business. We offer a hybrid working model, professional development opportunities, and the chance to be part of a global organization committed to operational excellence and continuous improvement.
Clinical Trial Associate Manager employer: Dormont Manufacturing Co
At Galderma, we pride ourselves on being an exceptional employer, offering a dynamic and collaborative work culture in the heart of London. As a Clinical Trial Associate Manager, you will not only lead a talented team but also benefit from our commitment to professional development and operational excellence, ensuring that your contributions have a meaningful impact on global clinical operations. With a hybrid working model and a focus on continuous improvement, Galderma provides a unique opportunity for growth and innovation in the clinical research field.
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We think this is how you could land Clinical Trial Associate Manager
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We think you need these skills to ace Clinical Trial Associate Manager
Some tips for your application 🫡
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