We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
We are looking for a Clinical Research Associate / Senior Clinical Research Associate to join a highly motivated, international team where collaboration, ownership, and trust are part of everyday work.
Hybrid role in Munich/Planegg or Home-based in Germany
You will:
What makes the role different:
As a privately owned mid-sized CRO, we are growing steadily and sustainably — with a strong focus on quality delivery, people, and long-term development. That means decisions are made close to the work, with real attention to what matters: patients, studies, and the people running them.
Why join us?
You will be part of an experienced, dynamic, and truly international team, where knowledge sharing and collaboration happen naturally across borders. You are not a number here — your contribution is visible, valued, and directly connected to study success.
We invest in structured onboarding and continuous mentoring, ensuring you are supported from day one and set up for long-term success. Many of our leaders today started in CRA roles internally — career progression is not an exception, but a well-established path.
You will work in a technologically integrated environment, with in-house systems designed to reduce administrative burden and keep your focus where it belongs: on high-quality site management and patient safety.
What you can expect:
If you are looking for a role where you can grow professionally, take ownership early, and be part of a supportive and highly capable team, we would be happy to receive your application.
Monitor clinical trials across therapeutic areas, ensuring site compliance, data quality, and participant safety while coordinating with investigators and project teams and mentoring less experienced associates.
Conduz avaliações complexas de risco toxicológico, define estratégias científicas para impurezas e contaminantes e prepara pareceres e justificativas regulatórias para submissões nacionais e internacionais.
Own monitoring and site management for complex clinical studies, ensuring protocol compliance, data quality, and participant safety while identifying risks, recommending corrective actions, and mentoring junior Clinical Operations staff.
Leads scientific safety activities for assigned products across development and post-marketing, driving surveillance, signal evaluation, aggregate assessments, benefit-risk analysis, and regulatory safety support.
Oversee clinical trial monitoring from pre-study through close-out, assess investigational site readiness, train site staff, support regulatory submissions, and mentor junior colleagues.
