Clinical Research Physician

Green Life Science; Düsseldorf; Remote; EUR 60.000 - 80.000; Teilzeit

Zusammenfassung

A leading clinical research organization is seeking a Sub-Investigator for musculoskeletal trials in Germany. This freelance/contract position offers the flexibility of full-time or part-time commitments, requiring a medical degree and experience in clinical trials. Ideal candidates will have orthopaedic expertise and proficiency in both English and German. The role involves assisting with clinical trial procedures, ensuring patient safety, and documentation support.

Leistungen

Flexibility in working hours

Opportunity to extend contract after 11 weeks

Qualifikationen

• License to practice medicine in Germany is required.
• Prior experience as a Sub-Investigator or in clinical trial support is preferred.
• Strong knowledge of GCP and clinical research practices.

Aufgaben

• Assist the Principal Investigator in conducting clinical trials according to protocol.
• Perform study-related procedures and ensure patient safety.
• Support documentation, data collection, and adverse event reporting.

Kenntnisse

Orthopaedic expertise

Clinical research knowledge

Fluent in English

Fluent in 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