SymBio.

Head of Clinical Operations (MedTech)

SymBio.

Leipzig, Saxony, Germany · Full Time

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Experience
5+ yrs
Salary
Openings
1
Posted
55 minutes ago
Work mode
In office
Education
Degree in Life Sciences, Medicine, Pharmacy, Biomedicine or related field
Resume
Required to apply

Where you'll work

Job description

Position Overview

We are seeking an experienced leader to take on the role of Head of Clinical Operations for a pioneering MedTech company in the Leipzig region. This role is initially contracted for two years with the possibility of extension to a permanent position.

Key Responsibilities

  • Assume strategic responsibility for all clinical study programs within the company.
  • Develop and execute a global strategy for Clinical Operations aligned to company goals.
  • Plan, direct, and monitor clinical studies ensuring adherence to timelines, quality standards, and budgetary constraints.
  • Ensure compliance with regulatory frameworks such as ICH-GCP and internal Standard Operating Procedures (SOPs).
  • Lead, develop, and expand the Clinical Operations team to meet operational needs.
  • Manage and oversee external partners including CROs, service providers, and investigation sites.
  • Responsible for managing clinical trials throughout their full lifecycle from initiation to closure.
  • Identify, assess, and resolve risks and challenges encountered during clinical studies.
  • Collaborate closely with internal departments such as Medical, Regulatory, and Quality teams.
  • Support audits, inspections, and communication with regulatory authorities.
  • Contribute to study protocols, regulatory submissions, and strategic development plans.
  • Report regularly to Senior Management and assist with board and investor presentations.

Candidate Requirements

  • Degree in Life Sciences, Medicine, Pharmacy, Biomedicine, or a related discipline.
  • A minimum of 5 years' experience in Clinical Operations, preferably within a MedTech environment focused on Class III medical devices.
  • In-depth understanding of ICH-GCP guidelines, ISO 14155, and relevant regulatory requirements.
  • Proven leadership experience managing teams and handling complex clinical trial programs.
  • Demonstrated expertise in managing global studies and coordination with external service providers.
  • Strong skills in strategic planning, organizational development, and problem-solving.
  • Excellent communication and leadership abilities.
  • Experience working in dynamic, fast-growing company environments.
  • Fluency in English with strong negotiation capabilities.

Benefits and Working Conditions

  • Key strategic position with substantial responsibility and direct impact on company objectives.
  • Collaboration with top-level management.
  • Engagement in an international, innovative workplace.
  • Opportunity to shape and develop processes and teams.
  • Work on clinically critical programs prioritizing quality and patient safety.
  • Dynamic setting characterized by rapid decision-making.

Work styles they’re looking for

Adaptability Leadership Problem Solving Cross-functional Collaboration Communication Skills Strategic Thinking Strategic Planning Team leadership and development Audit and Regulatory Communication

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