Aktiviere Job-Benachrichtigungen per E-Mail!

Clinical Research Physician

Green Life Science

Leipzig

Remote

EUR 40.000 - 60.000

Teilzeit

Heute
Sei unter den ersten Bewerbenden

Zusammenfassung

A clinical research organization is seeking a Sub-Investigator to support musculoskeletal trials in Germany. This freelance role allows for full-time or part-time commitment, preferably for candidates with orthopaedic experience. The role involves assisting with clinical trials, ensuring patient safety, and supporting documentation and data collection. Fluency in English and German is required, alongside a medical degree.

Qualifikationen

  • Medical degree with a license to practice in Germany.
  • Prior experience as a Sub-Investigator or in clinical trial support.
  • Strong knowledge of GCP and clinical research practices.

Aufgaben

  • Assist the Principal Investigator in conducting clinical trials.
  • Perform study-related procedures and ensure patient safety.
  • Support documentation, data collection, and adverse event reporting.
  • Collaborate with site staff and sponsor teams.

Kenntnisse

Orthopaedic experience
Knowledge of GCP
Fluent in English and German

Ausbildung

Medical degree (MD or equivalent)
Jobbeschreibung
Overview

Sub-Investigator (Freelance / Contract) – Musculoskeletal Trials (Germany)

Sub-Investigator to support upcoming clinical research projects in Germany. This can be a full-time or part-time freelance / contract role within the musculoskeletal therapeutic area, with preference for those with orthopaedic experience.

Position Details
  • Role : Sub-Investigator (Contractor)
  • Therapeutic Area : Musculoskeletal (orthopaedics preferred)
  • Commitment : up to 40 hours per week
  • Duration : Minimum 11 weeks, with strong extension potential
  • Location : Remote - Germany
  • Start Date : November 7th
Responsibilities
  • Assist the Principal Investigator in conducting clinical trials according to protocol, GCP, and regulatory requirements
  • Perform study-related procedures and ensure patient safety
  • Support documentation, data collection, and adverse event reporting
  • Collaborate with site staff and sponsor teams to ensure trial quality and integrity
Requirements
  • Medical degree (MD or equivalent) with license to practice in Germany
  • Prior experience as a Sub-Investigator or in clinical trial support
  • Orthopaedic or musculoskeletal experience strongly preferred
  • Strong knowledge of GCP and clinical research practices
  • Fluent in English and German
Company
  • Delivering trials 4x faster than traditional CROs
  • 80+ trials completed across EU & US
  • Patient-centric, tech-enabled model accelerating access to new treatments
Hol dir deinen kostenlosen, vertraulichen Lebenslauf-Check.
eine PDF-, DOC-, DOCX-, ODT- oder PAGES-Datei bis zu 5 MB per Drag & Drop ablegen.