AD

Study Site Specialist

Eckdaten

Deutschland
Research

Arbeitsmodell

Vollständig remote
Nur DE
vor 1 Woche
Stellenbeschreibung

Study Site Specialist (Entry Level) -- FSP | Permanent | Remote (Germany)

Location: Germany (Remote)

Work Model: Fully remote (WFH)

Who This Role Is For

This position is ideal for candidates looking to build a career in clinical research and a start-up.

You might be a strong fit if you have:

  • Around 1--2 years of experience in clinical research, or
  • Completed a placement/internship within a CRO, pharma, or research setting , or
  • An academic background in life sciences with exposure to clinical research concepts

If you're early in your career and looking for a structured environment to develop within clinical operations, this is a solid entry point.

About the Role

This is a permanent FSP (Functional Service Provider) position , supporting global clinical trials with a focus on site start-up activities.

Working under the guidance of experienced Study Start-Up and Study Support teams, you will be involved in the end-to-end process of activating clinical trial sites, from feasibility through to site initiation.

You'll gain hands-on exposure to how clinical trials are set up across different countries and healthcare systems.

Key Responsibilities

  • Support site start-up activities from feasibility through to activation
  • Act as a point of contact for study teams, supporting start-up coordination
  • Assist with site identification and feasibility processes
  • Help collect, track, and review essential site documentation
  • Support contract and budget coordination activities (with guidance)
  • Contribute to Ethics Committee and Regulatory Authority submissions
  • Use internal tools to track progress and maintain accurate records
  • Support country- and site-level requirements for study activation
  • Collaborate with internal teams to ensure timelines are met

Your Background

  • Degree in Life Sciences or related field
  • 1--2 years' experience in clinical research or a relevant placement/internship
  • Basic understanding of clinical trials and drug development
  • Familiarity with ICH-GCP principles is an advantage
  • Strong organisational skills and attention to detail
  • Confident using MS Office (Excel, Word, Outlook, PowerPoint)
  • Good written and verbal communication skills in English
  • Eagerness to learn and develop within a structured, team environment

Additional Information

  • Fully remote role within Germany
  • No travel required
  • Opportunity to grow within a structured FSP model with clear career progression (Specialist → Specialist II → Senior levels)

Final Note

This is a junior-level opportunity , and the role and compensation are aligned accordingly. It's best suited to candidates who are early in their careers and motivated to build experience in a clinical trial start-up.