Clinical Research Associate (Oncology)

TL;DR

Clinical Research Associate (Oncology): Monitoring and owning the progress of clinical studies at investigative sites with an accent on ICH-GCP compliance and regulatory standards. Focus on coordinating study setup, performing initiation visits, and identifying potential study risks to ensure high-quality clinical outcomes.

Location: Remote, Germany (Requires 50-60% domestic travel)

Company

hirify.global is a precision medicine CRO specializing in oncology and rare diseases, utilizing biomarkers and advanced data analytics to optimize drug development.

What you will do

• Monitor and manage the progress of clinical studies at investigative sites.
• Ensure all studies are conducted and reported according to protocols, SOPs, and ICH-GCP standards.
• Coordinate site setup activities, including investigator identification and regulatory submissions.
• Conduct pre-study and initiation visits to ensure site readiness.
• Identify potential study risks and propose effective mitigation strategies.

Requirements

• Graduate or postgraduate degree in a scientific or healthcare discipline.
• Minimum 1 year of experience as a CRA within a CRO, pharmaceutical, or biotech environment.
• Fluency in English and German is required.
• Experience in oncology, CAR-T, or Phase III FIH studies.
• Must be based in Germany with availability for 50-60% domestic travel.

Nice to have

• Experience with study start-up activities.
• Experience working with medical devices.

Culture & Benefits

• Strong work-life balance with a low study load (average 1-2 studies per CRA).
• High employee retention rates and supportive line management.
• Collaborative environment in a smaller CRO where individual input has a significant impact.
• Culture focused on professional growth and valuing employee contributions.