Part Time Contractor (Clinical Data Manager) - EU

Ergomed; Frankfurt; Vor Ort; EUR 45.000 - 75.000; Vollzeit

Zusammenfassung

An established industry player is seeking a Clinical Data Manager for a 3-month contract. This role involves overseeing data management activities, training staff, and ensuring high-quality deliverables. You'll work in a collaborative environment, contributing to meaningful projects that enhance lives. With a strong emphasis on personal and professional growth, this position offers a friendly and supportive workplace culture. Join a diverse team and make a difference while advancing your career in the pharmaceutical industry.

Leistungen

Training and career development opportunities

Emphasis on personal and professional growth

Supportive working environment

Opportunity to work with international colleagues

Qualifikationen

• 3-5 years of experience in data management within the pharmaceutical industry.
• Proficiency in EDC systems and common computer applications.

Aufgaben

• Oversee Data Management activities and provide project updates.
• Train staff and manage data review and query management.

Kenntnisse

Data Management

EDC Systems

Windows

Excel

Word

Outlook

Tools

Merative Zelta

Jobbeschreibung

We are looking for a highly qualified Clinical Data Manager for a 3-month contract at 0.5 FTE.

Responsibilities

1. Provide oversight of all Data Management activities within the ERGOMED Data Management (DM) department in a collaborative team environment.
2. Update and communicate Data Management progress during internal and client team meetings.
3. Generate metric reports for internal and external project teams.
4. Train other DM staff on project-specific processes.
5. Provide feedback to project team members and managers to enhance deliverables.
6. Review data management documentation including Data Management Plan, Data Review Plan, eCRF Completion Guidelines, etc.
7. Communicate project risks or quality issues to the Project Data Manager.
8. Manage Lab ranges across the entire study.
9. Perform data review and query management activities.
10. Oversee the issuance of queries and review query responses to ensure high quality.

Qualifications

1. 3-5 years of relevant experience in the pharmaceutical industry or contract research organization, specifically in data management.
2. Experience working with EDC systems (e.g., Merative Zelta).
3. Proficiency in computer applications such as Windows, Excel, Word, Outlook.

Additional Information

We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders, and ages can contribute and grow.

To succeed, we must work together with a human-first approach because our people are our greatest strength, leading to our continued success in improving lives.

What We Offer

• Training and career development opportunities internally.
• Strong emphasis on personal and professional growth.
• A friendly, supportive working environment.
• Opportunity to work with colleagues worldwide, with English as the company language.