Clinical Research Coordinator // Heidelberg, Germany

R&D Partners; Heidelberg; Vor Ort; EUR 83.000 - 96.000; Teilzeit

Zusammenfassung

R&D Partners in Heidelberg is seeking a dedicated Research Coordinator to support pulmonology clinical trials. This part-time role involves documenting study activities, coordinating patient visits, data entry, and liaising with external vendors to ensure smooth trial operations.

You will manage lab samples, submit reports and imaging, and maintain trial files while upholding ICH-GCP standards. Fluency in English and valid IATA certification are required.

Qualifikationen

• Experience in clinical trials as a Study Nurse or Study Coordinator.
• Familiarity with pulmonology studies and terminology.
• Knowledge of electronic data capture systems like Inform and Veeva EDC.
• Ability to use laboratory reporting applications.
• Strong communication skills and a professional, patient-friendly approach.
• Completed ICH-GCP training within the last 12 months.
• Valid IATA certification with at least six months before expiration.
• Fluent in English, both written and spoken.

Aufgaben

• Organize and maintain study-related documents.
• Enter and manage data in electronic systems, resolving any issues that arise.
• Handle, process, and ship lab samples to international labs.
• Submit lab reports and imaging files to external service providers.
• Communicate with vendors and service providers.
• Prepare for patient visits and schedule appointments.
• Keep patient and investigator site files up to date.
• Attend monitoring visits to ensure compliance with study protocols.

Kenntnisse

Clinical trials experience

Pulmonology knowledge

EDC systems: Inform/Veeva

Lab data handling

Communication & teamwork

ICH-GCP training (recent)

IATA certification

English fluency

Tools

Inform EDC

Veeva EDC

Jobbeschreibung

Looking to be the heartbeat of clinical research? Our client is searching for a Research Coordinator to assist in turning innovative science into life-changing care!

R&D Partners is seeking a dedicated and detail-oriented Study Coordinator to support clinical trial activities in the field of pulmonology. This role involves assisting with study documentation, managing patient visits, coordinating with external vendors, and ensuring smooth trial operations. The position is part-time, offering flexibility from Monday to Friday, and is based onsite in Heidelberg.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Help organize and maintain study-related documents.
• Enter and manage data in electronic systems, resolving any issues that arise.
• Handle, process, and ship lab samples to international labs.
• Submit lab reports and imaging files to external service providers.
• Communicate with vendors and service providers.
• Prepare for patient visits and schedule appointments.
• Keep patient and investigator site files up to date.
• Attend monitoring visits to ensure compliance with study protocols.

Key Skills and Requirements:

• Experience working in clinical trials as a Study Nurse or Study Coordinator.
• Familiarity with pulmonology studies and related terminology.
• Knowledge of electronic data capture systems like Inform and Veeva EDC.
• Ability to use laboratory reporting applications.
• Strong communication skills and a professional, patient-friendly approach.
• Team-oriented mindset with excellent collaboration skills.
• Completed ICH-GCP training within the last 12 months.
• Valid IATA certification with at least six months before expiration.
• Fluent in English, both written and spoken.
• €60 to €70 per hour.

For more information, please contact Terrah-Leigh Pietersen.

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