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- Aufgaben: Lead clinical safety activities and manage large programs in a dynamic team environment.
- Arbeitgeber: Join Medpace, a top-tier CRO dedicated to advancing medical therapeutics globally.
- Mitarbeitervorteile: Enjoy flexible work options, competitive pay, and structured career growth opportunities.
- Warum dieser Job: Make a real impact on patient lives while developing your expertise in a supportive culture.
- Gewünschte Qualifikationen: Bachelor's or Master's degree with relevant clinical safety experience and strong leadership skills required.
- Andere Informationen: This role is office-based in Munich; applications should be submitted in English.
Das voraussichtliche Gehalt liegt zwischen 43200 - 72000 € pro Jahr.
Job Summary
Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Clinical Safety Manager to join our team in Munich. 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 can use your previous expertise and 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 and study reports.
- Create safety management plans dependent upon client needs.
- 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.
Please note this role is office-based in Munich.
Qualifications
- Bachelor’s degree and 5 years of clinical safety experience, including project management and ideally line management experience; OR
- Master\’s degree and 3 years of clinical safety experience, including project management and ideally line management experience.
- Previous experience of managing clinical safety activities for multiple programs.
- 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.
We kindly ask to submit applications in English.
Medpace Overview
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?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas.
Medpace Perks
- 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.
Awards
- Recognized by Forbes as one of America\’s Most Successful Midsize Companies in 2021, 2022, 2023, and 2024.
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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Clinical Safety Manager - Pharmacovigilance / Drug Safety Arbeitgeber: Medpace
Kontaktperson:
Medpace HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Clinical Safety Manager - Pharmacovigilance / Drug Safety
✨Tip Number 1
Familiarize yourself with the latest global clinical safety regulatory requirements. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in pharmacovigilance and drug safety. Attend industry conferences or webinars to connect with potential colleagues and learn more about the current trends and challenges in clinical safety.
✨Tip Number 3
Prepare to discuss your experience in managing clinical safety activities for multiple programs. Be ready to provide specific examples of how you've successfully handled complex projects and client relationships.
✨Tip Number 4
Showcase your leadership and mentoring skills during the interview process. Think of instances where you've led a team or mentored colleagues, as these experiences align well with the responsibilities of the Clinical Safety Manager role.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Clinical Safety Manager - Pharmacovigilance / Drug Safety
Tipps für deine Bewerbung 🫡
Tailor Your CV: Make sure your CV highlights your clinical safety experience, project management skills, and any relevant line management experience. Use keywords from the job description to align your qualifications with what Medpace is looking for.
Craft a Strong Cover Letter: Write a cover letter that emphasizes your passion for pharmacovigilance and your ability to manage clinical safety activities. Mention specific experiences that demonstrate your expertise and how you can contribute to Medpace's mission.
Highlight Relevant Experience: In your application, focus on your previous roles related to clinical safety, especially those involving SOP writing, PSMF generation, and aggregate reporting. Provide examples of how you've successfully managed multiple programs.
Proofread Your Application: Before submitting, carefully proofread your application materials for any grammatical or spelling errors. Clear and professional communication is crucial, especially in a role that requires excellent verbal and written skills.
Wie du dich auf ein Vorstellungsgespräch bei Medpace vorbereitest
✨Showcase Your Clinical Safety Expertise
Be prepared to discuss your previous clinical safety experience in detail. Highlight specific projects you've managed, particularly those involving multiple programs, and how you ensured high-quality outcomes.
✨Demonstrate Strong Communication Skills
Since the role requires excellent verbal and written communication skills, practice articulating your thoughts clearly. Be ready to provide examples of how you've effectively communicated with clients and stakeholders in past roles.
✨Prepare for Teamwork Scenarios
Expect questions about teamwork and collaboration. Think of instances where you successfully worked within a team to achieve a common goal, especially in a clinical safety context.
✨Familiarize Yourself with Regulatory Requirements
Brush up on global clinical safety regulatory requirements. Being able to discuss these regulations confidently will demonstrate your comprehensive knowledge and readiness for the role.
