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Medpace

Global CRO delivering full-service clinical trials

Clinical Safety Manager - Pharmacovigilance / Drug Safety

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeMunich, GermanyNo salary listed

About the Job

Requirements

  • A bachelor's degree and 5 years of clinical safety experience, including project management and ideally line management experience, or a master's degree and 3 years of clinical safety experience, including project management and ideally line management experience.
  • Previous experience managing clinical safety activities for multiple programs.
  • Experience writing departmental standard operating procedures and work instructions.
  • Experience generating and maintaining a Pharmacovigilance System Master File.
  • Experience writing and maintaining Company Core Data Sheets, Risk Management Plans, and Summary of Product Characteristics.
  • 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.

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 the client.
  • Attend business development activities such as presentations to prospective sponsors, participation in sponsor audits, and generation of scopes of work and cost estimates.
  • Write departmental standard operating procedures and work instructions.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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