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Clincial Research Associate / Senior CRA

Garching bei München, München (Kreis)💼 Full-time🗓 2026-07-03 → 2026-07-31

Core

Managing clinical trial operations, overseeing budgets, and leading a team of Clinical Research Associates to ensure effective study oversight and timely enrollment.

Role type

Senior Clinical Trial Manager

Builds

Clinical trial programs for sponsors

Domain

Healthcare / Clinical Research / Oncology

Deliverable

client delivery

Required skills

Clinical trial management, budget oversight, study oversight planning, team mentoring, study start-up and enrollment management, corrective and preventative action planning, stakeholder relationship management

Preferred skills

Monitoring experience, managing complex or global trials, managing all trial components from start-up to database lock, coaching/mentoring other CTMs

Technologies

None stated

Responsibilities

Oversee the clinical portion of the budget, develop monitoring plans and tools, train and mentor Clinical Research Associates, drive enrollment and lead study start-up activities, review trip reports and implement corrective and preventative action plans

Seniority

Senior, hands-on IC with team leadership

Rewrite
## Responsibilities As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability. * **Budget Oversight:** Oversee the clinical portion of the budget to ensure efficient resource allocation. * **Ensuring Effective Study Oversight:** Develop monitoring plans and tools, ensuring effective study oversight. * **Optimizing Performance:** Train and mentor Clinical Research Associates (CRAs) to optimize their performance. * **Timely Study Start-Up & Enrollment:** Drive enrollment and lead study start-up activities, adhering to timelines. * **Improving Study Integrity:** Review trip reports and implement corrective and preventative action plans when necessary. * **Building Productive Relationships:** Foster productive relationships with Sponsors, vendors, and cross-functional teams. ## Requirements * A minimum of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization. * Bachelor's degree in health, life sciences, or other relevant fields of study. * At least 10+ years of relevant experience in clinical trial management. * Fluency in German and English language. * Willingness to travel as required (approximately 25%). ## Nice to Have * 2+ years of monitoring experience. * Experience in managing complex or global trials. * Experience in managing all trial components from start-up to database lock. * Experience in coaching/mentoring other CTMs, leading a team of CTMs, and participating in departmental initiatives. ## Benefits * Various annual leave entitlements. * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance. * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
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