At a Glance
- Tasks: Lead clinical safety activities and manage large programmes in a dynamic team.
- Company: Join Medpace, a leading clinical research organisation with a collaborative culture.
- Benefits: Enjoy competitive pay, health benefits, and opportunities for remote work.
- Other info: Experience continuous growth with defined career paths and ongoing training.
- Why this job: Make a real impact on global health by advancing medical therapeutics.
- Qualifications: Bachelor's degree and clinical safety experience required; strong leadership skills preferred.
The predicted salary is between 54000 - 66000 £ 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 London. 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
Qualifications
- 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 Overview
Medpace is a full-service clinical contract research organization (CRO) providing 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
- Purpose-Driven Work: Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
- Collaborative Culture: Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust. Leadership throughout Medpace is both accessible and approachable
- Continuous Growth & Development: Office based environment with on-site mentors. Defined career paths with clear advancement opportunities. Industry renowned onboarding and training programs designed to accelerate professional development. Ongoing training and continuous learning opportunities throughout your career. An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Flexible Clinical Safety Lead – Pharmacovigilance in London employer: Medpace
Medpace is an exceptional employer, offering a collaborative and purpose-driven work environment in Cincinnati, Ohio, where employees can thrive alongside industry-leading experts in clinical research. With a strong focus on continuous learning and professional development, Medpace provides defined career paths, comprehensive benefits, and a culture that encourages innovation and employee contributions. Join us to make a meaningful impact on global health while enjoying competitive compensation and a supportive office-based atmosphere.
StudySmarter Expert Advice🤫
We think this is how you could land Flexible Clinical Safety Lead – Pharmacovigilance in London
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like Medpace. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
✨Join Relevant Professional Bodies
Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like Medpace.
✨Leverage Internships for Full-time Roles
If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like Medpace. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.
✨Tailor Your Approach
When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what Medpace is looking for. A tailored application can really make you stand out!
We think you need these skills to ace Flexible Clinical Safety Lead – Pharmacovigilance in London
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Medpace!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Medpace that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Medpace!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Medpace, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Medpace
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Medpace that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Medpace’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
