Clinical Research Associate (Germany)

TL;DR

Clinical Research Associate (Clinical Trials): Managing clinical study sites and ensuring protocol compliance with an accent on independent monitoring, data integrity, and site relationship management. Focus on executing site visits, resolving data queries, and managing CAPA plans to ensure high-quality clinical trial delivery.

Location: Must be based in Germany, preferably in the northern part

Company

hirify.global is a mid-sized, global Contract Research Organisation (CRO) specializing in Phase I–IV clinical studies and full-service clinical development solutions.

What you will do

• Perform independent site visits including pre-study, initiation, monitoring, and closeout.
• Manage site personnel to ensure compliance, enrollment targets, and study understanding.
• Review CRFs and manage query generation and resolution.
• Identify and escalate risks while providing retraining for site staff.
• Develop and track corrective and preventive (CAPA) plans.
• Negotiate study budgets and assist with site contract execution.

Requirements

• University degree in medical or life sciences or nursing education.
• 2–3 years of independent clinical trial monitoring experience in a CRO or pharma environment.
• Strong knowledge of ICH GCP Guidelines and regulatory requirements.
• Fluent in German and English (written and verbal).
• Valid driver’s license.
• Ability to work independently and effectively in a matrix environment.

Culture & Benefits

• Performance and referral bonuses with a sign-on bonus included.
• Flexible work hours.
• Training and professional development programs.
• Employee engagement and well-being initiatives.
• Shopping discounts.
• International project exposure within a growing global team.