Clinical Research Coordinator / Heidelberg, Germany

R Dpartners; Heidelberg; Vor Ort; EUR 83.000 - 96.000; Teilzeit

Zusammenfassung

R&D Partners seeks a dedicated Research Coordinator to support pulmonology clinical trials onsite in Heidelberg. The role focuses on study documentation, data entry, and coordination with external vendors to ensure smooth trial operations.

Ideal candidates will have study coordination experience, ICH-GCP training, and both German (native) and English language proficiency to communicate with international labs and sites.

Qualifikationen

• Experience in clinical trials as 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 and a professional, patient-friendly approach.
• ICH-GCP training within the last 12 months.
• Native-level German proficiency and fluent English.

Aufgaben

• Help organize and maintain study-related documents.
• Enter and manage data in electronic systems, resolving issues.
• 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 protocol compliance.

Kenntnisse

Study coordination

Clinical trials

Data entry

Vendor coordination

Communication

Tools

Inform

Veeva EDC

Lab reporting apps

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.
• Native-level German proficiency.
• Fluent in English, both written and spoken.

Salary:

• €60 to €70 per hour.