Freelancer-Study Coordinator

ProPharma; Remote; EUR 30.000 - 45.000; Teilzeit

Zusammenfassung

A clinical research organization is seeking a detail-oriented Central Study Coordinator for a part-time role in Germany. The position involves coordinating clinical research activities, maintaining documentation, and ensuring compliance with standards. Ideal for candidates with a Bachelor’s degree in Life Sciences and a year of relevant experience. Proficiency in German is a must. This remote opportunity offers flexibility within a dynamic clinical research environment.

Qualifikationen

• Bachelor’s degree in Life Sciences, Nursing, or a related field.
• 1 year of experience as a CRA, CTA, or in study coordination preferred.
• Strong understanding of GCP and clinical research processes.

Aufgaben

• Support day-to-day coordination of clinical study operations.
• Maintain study documentation, trackers, and logs.
• Serve as a communication point between study sites and internal teams.
• Assist with study start-up activities.
• Track enrollment and site performance metrics.
• Perform quality checks on study documents.
• Coordinate study meetings and prepare agendas.
• Support monitoring activities and issue resolution.

Kenntnisse

Excellent communication

Time-management

Organizational skills

Understanding of Good Clinical Practice

Proficiency with study management systems

Fluency in German

Ausbildung

Bachelor’s degree in Life Sciences

Nursing

Public Health

Tools

Microsoft Office Suite

Jobbeschreibung

Position : Central Study Coordinator

Location : Remote,Germany

Employment Type : Part-time – 0.6 (Freelance Contract)

Industry : Clinical Research / Life Sciences

About the Role

We are seeking a detail-oriented and proactive Central Study Coordinator to support the planning, execution, and oversight of clinical research studies. This remote opportunity within Germany serves as a central operational hub—coordinating study activities, maintaining study documentation, assisting site teams, and ensuring all study processes align with regulatory and sponsor requirements.

This position is ideal for candidates looking for a part-time role within a dynamic clinical research environment

Key Responsibilities

• Support day-to-day coordination of clinical study operations.
• Maintain study documentation, trackers, logs, and study management systems.
• Serve as a central point of communication between study sites, vendors, and internal teams.
• Assist with study start-up activities, including document collection and site readiness.
• Track enrollment, site performance metrics, and study timelines.
• Perform quality checks on study documents to ensure compliance with GCP, SOPs, and regulatory standards.
• Coordinate study meetings, prepare agendas, and document meeting minutes.
• Support monitoring activities by assisting with follow-ups, reconciliation tasks, and issue resolution.
• Contribute to the development and review of study materials such as training guides, manuals, and plans.

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, Public Health, or a related field.
• 1 year of experience as a CRA, CTA, or study coordination experience preferred.
• Strong understanding of Good Clinical Practice (GCP) and clinical research processes.
• Excellent communication, time-management, and organizational skills.
• Proficiency with study management systems and Microsoft Office Suite.
• Ability to work effectively in an on-site, team-oriented environment.
• German spoken to professional level