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- Tasks: Lead clinical safety activities and manage multiple large programmes in a dynamic team environment.
- Company: Medpace is a global CRO dedicated to accelerating the development of safe medical therapeutics.
- Benefits: Enjoy flexible work options, competitive pay, and structured career growth opportunities.
- Why this job: Make a real impact on patient lives while developing your skills in a supportive culture.
- Qualifications: Bachelor's degree with clinical safety experience; strong leadership and communication skills required.
- Other info: Join a company recognised by Forbes for its success and commitment to quality.
The predicted salary is between 36000 - 60000 £ per year.
Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Manager to join our UK team and to be based at our growing UK office in Stirling. This position plays a key role in the pharmacovigilance process at Medpace. Working in a team to accomplish tasks and projects that are instrumental to the company’s success.
If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
Responsibilities- Manage Clinical Safety activities and multiple large programs
- Manage relationships with clients and internal stakeholders by providing expert safety knowledge
- Oversee clinical safety case management and aggregate reporting responsibilities to ensure client needs are fulfilled to a high quality
- Provide safety review of clinical study documents, including protocols, study reports; and marketing application components
- Create safety management plans dependent upon client
- Attend business development activities such as presentations to prospective Sponsors, participation in Sponsor audits, generation of scope of work and cost estimates
- Write departmental SOPs and Work Instructions
- Bachelor’s degree or equivalent and clinical safety experience, including project management and ideally line management experience
- Previous experience of managing clinical safety activities for multiple programmes
- Experience in writing departmental SOPs and Work Instructions
- Experience in PSMF generation and maintenance
- Experience in CCDS/RMP/SmPC writing and maintenance
- Comprehensive knowledge of global clinical safety regulatory requirements
- Excellent verbal and written communication skills
- Strong leadership, mentoring, and motivational skills
- Exceptional teamwork skills
- Ability to work independently
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.
Why Medpace?
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Clinical Safety Manager - Pharmacovigilance / Drug Safety employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Safety Manager - Pharmacovigilance / Drug Safety
✨Tip Number 1
Familiarise yourself with the latest pharmacovigilance regulations and guidelines. Understanding the current landscape will not only help you in interviews but also demonstrate your commitment to the field.
✨Tip Number 2
Network with professionals in the clinical safety and pharmacovigilance sectors. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in the field.
✨Tip Number 3
Prepare to discuss specific case studies or experiences where you've successfully managed clinical safety activities. Highlighting your hands-on experience can set you apart from other candidates.
✨Tip Number 4
Research Medpace's recent projects and achievements in pharmacovigilance. Being knowledgeable about the company’s work will allow you to tailor your conversation during interviews and show genuine interest in their mission.
We think you need these skills to ace Clinical Safety Manager - Pharmacovigilance / Drug Safety
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant clinical safety experience, particularly in pharmacovigilance and project management. Use specific examples that demonstrate your expertise in managing clinical safety activities.
Craft a Strong Cover Letter: Write a cover letter that clearly outlines your motivation for applying to Medpace and how your skills align with the responsibilities of the Clinical Safety Manager role. Mention your experience in writing departmental SOPs and your knowledge of global regulatory requirements.
Highlight Leadership Skills: Since the role requires strong leadership and mentoring abilities, provide examples of how you've successfully led teams or projects in the past. This will show that you can manage relationships with clients and internal stakeholders effectively.
Proofread Your Application: Before submitting your application, thoroughly proofread all documents for spelling and grammatical errors. A polished application reflects your attention to detail, which is crucial in the field of clinical safety.
How to prepare for a job interview at Medpace
✨Showcase Your Clinical Safety Knowledge
Make sure to brush up on your understanding of pharmacovigilance and drug safety regulations. Be prepared to discuss your previous experiences in managing clinical safety activities and how they relate to the role.
✨Demonstrate Leadership Skills
As a Clinical Safety Manager, you'll need strong leadership abilities. Prepare examples of how you've successfully led teams or projects in the past, highlighting your mentoring and motivational skills.
✨Prepare for Technical Questions
Expect questions related to clinical study documents, SOPs, and safety management plans. Familiarise yourself with the specifics of writing and maintaining these documents, as well as your experience with PSMF generation.
✨Engage with the Interviewers
Show enthusiasm for the role and the company. Ask insightful questions about Medpace's projects and culture, demonstrating your interest in contributing to their mission of improving patient lives.
