Job Title: Sub-Investigator / Co-Investigator (Contractor)
Location: Germany (Remote/On-site as required)
Employment Type: Freelance / Contractor
Commitment: 13 hours per week
Duration: 3 months (with potential extension)
Support Clinical Trials as a Sub-Investigator in Germany
We are recruiting a Sub-Investigator / Co-Investigator in Germany to support a leading clinical research organization (CRO) on key ongoing studies. This flexible freelance opportunity is ideal for licensed physicians with clinical research experience who want to work 13 hours per week across various therapeutic areas.
This is a remote-first position, with occasional on-site involvement based on study needs.
Key Responsibilities
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Assist the Principal Investigator in delivering clinical trials according to study protocols and ICH-GCP guidelines
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Support patient recruitment, informed consent, and protocol-driven clinical assessments
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Accurately document patient data in source notes and electronic data capture systems
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Collaborate with site staff and sponsor teams to ensure data quality and protocol compliance
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Participate in site monitoring visits, audits, and regulatory inspections as required
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Help with safety reporting, managing deviations, and resolving data queries
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Maintain compliance with EU Clinical Trial Regulation and German health authorities
Candidate Requirements
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MD or equivalent medical qualification; must be a licensed physician in Germany
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1–2 years of prior experience in clinical research or a previous role as a Sub-Investigator / Co-Investigator
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Proficient knowledge of ICH-GCP and local regulatory standards
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Fluent in German (spoken and written); English proficiency required for documentation
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Strong organizational, interpersonal, and communication skills
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Ability to commit 13 hours per week over the 3-month period
Contract Details
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Contract Type: Freelance
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Hours: 13 hours per week
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Duration: 3 months, with potential for renewal
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Location: Based in Germany; remote with occasional site visits depending on study needs
Why Join This Clinical Research Opportunity?
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Play a vital role in advancing clinical development across key therapeutic areas
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Collaborate with a reputable CRO recognized for high standards in patient care and data integrity
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Maintain flexibility with a part-time contractor model
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Build valuable experience in a dynamic, regulated research environment
How to Apply
📧 Send your CV to Alex Smith at: Alex@greenlsr.com
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