Job Description:
We are hiring a Clinical Trial Design Specialist in Berlin to develop clinical protocols and study designs that support regulatory approval and scientific advancement. You will work closely with medical writers, statisticians, and regulatory affairs to draft phase I–IV clinical protocols.
This role requires strong analytical and strategic skills to ensure scientifically sound and ethically compliant trial plans. You'll also participate in feasibility studies and risk assessments, ensuring GCP standards are met throughout the trial process.
This position is ideal for a candidate with a strong clinical research background and a passion for clinical innovation.
Job Requirement:
Advanced degree (MD, PharmD, MSc) in Life Sciences or Clinical Research
5+ years of experience in clinical trial protocol development
Familiarity with ICH-GCP and EU Clinical Trials Regulation
Experience in cross-functional clinical development teams
Proficiency in statistical concepts and trial design methodologies
Strong writing and communication skills
Knowledge of therapeutic areas such as oncology or neurology is a plus
Ability to analyze complex data and translate it into clinical strategy
Fluent in English; German preferred
Experience working with CROs and regulatory bodies
