Global Clinical Trial Coordinator (mwd), German Speaking, Home-Office in DACH

Frankfurt - Germany

Monthly Salary: Not Disclosed

Posted on: 17 hours ago

Vacancies: 1 Vacancy

Job Summary

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our clients project team in the execution of early clinical trials. Joining our team offers the opportunity to work on innovative projects in a dynamic environment. You will support trial preparation documentation and coordination ensuring compliance with regulatory standards and internal processes. This role combines operational and administrative responsibilities and requires close collaboration with internal and external stakeholders.

We currently offer an exciting opportunity to join the FSP team as global Clinical Trial Coordinator ECT (m/w/d) in full-time and work home-based throughout Germany Austria and Switzerland.

RESPONSIBILITIES

Coordinate clinical trials in early clinical development for both Sponsor and Study site.
Support Clinical Trial Leaders Clinical Trial Managers Clinical Research Associates and Principal Investigators in all study-related activities throughout all study phases (preparation conduct close-out).
Prepare and manage clinical trial documentation
Compilation and collection of submission documents.
Maintain trial-specific data and timelines in electronic systems.
Communicate effectively with internal and external partners (e.g. statisticians data managers regulatory affairs investigators).
Organize and monitor study-related activities meetings and documentation.
Ensure timely preparation of submission documents for authorities and ethics committees.
Manage essential documents for Investigator Site File (ISF) and ensure Trial Master File (TMF) completeness and compliance.
Act as TMF Records Specialist: oversee TMF strategy perform quality checks maintain List of Expected Records and ensure audit/inspection readiness.
Participate in process harmonization initiatives and support implementation of new systems.
Assist in finalizing Clinical Trial Reports (CTR) and appendices.

REQUIRED KNOWLEDGE SKILLS AND EXPERIENCE

Bachelors or higher-level degree in Business Administration Life Science or equivalent with experience in clinical trials.
Alternatively vocational training with extensive experience in clinical and regulatory environments.
At least 5 years experience as Clinical Trial Coordinator or within a similar role in clinical research.
Strong knowledge of applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Excellent administrative and organizational skills.
Strong communication and interpersonal skills.
Proficiency in MS Office and eTMF systems (e.g. Veeva BIRDS).
Fluent languages skills in German on at least C1 level and good command of English.
Ability to work independently prioritize tasks and manage multiple projects in a complex international environment.

WHAT YOU CAN EXPECT

Permanent employment contract.
In-depth training and mentoring.
Home-Office throughout Germany Austria or Switzerland.
Competitive salary and benefits package.
If you are located in Austria: Monthly gross salary is starting at 3.600 EUR basic - an overpay according to skills and working experience is possible. The monthly gross salary in all other countries will be different to this.

We invite you to join IQVIA!

Please apply with your English CV motivation letter and education certificates and job reference letter.

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at

Required Experience:

RESPONSIBILITIES

Coordinate clinical trials in early clinical development for both Sponsor and Study site.
Support Clinical Trial Leaders Clinical Trial Managers Clinical Research Associates and Principal Investigators in all study-related activities throughout all study phases (preparation conduct close-out).
Prepare and manage clinical trial documentation
Compilation and collection of submission documents.
Maintain trial-specific data and timelines in electronic systems.
Communicate effectively with internal and external partners (e.g. statisticians data managers regulatory affairs investigators).
Organize and monitor study-related activities meetings and documentation.
Ensure timely preparation of submission documents for authorities and ethics committees.
Manage essential documents for Investigator Site File (ISF) and ensure Trial Master File (TMF) completeness and compliance.
Act as TMF Records Specialist: oversee TMF strategy perform quality checks maintain List of Expected Records and ensure audit/inspection readiness.
Participate in process harmonization initiatives and support implementation of new systems.
Assist in finalizing Clinical Trial Reports (CTR) and appendices.

REQUIRED KNOWLEDGE SKILLS AND EXPERIENCE

Bachelors or higher-level degree in Business Administration Life Science or equivalent with experience in clinical trials.
Alternatively vocational training with extensive experience in clinical and regulatory environments.
At least 5 years experience as Clinical Trial Coordinator or within a similar role in clinical research.
Strong knowledge of applicable clinical research regulatory requirements i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Excellent administrative and organizational skills.
Strong communication and interpersonal skills.
Proficiency in MS Office and eTMF systems (e.g. Veeva BIRDS).
Fluent languages skills in German on at least C1 level and good command of English.
Ability to work independently prioritize tasks and manage multiple projects in a complex international environment.

WHAT YOU CAN EXPECT

Permanent employment contract.
In-depth training and mentoring.
Home-Office throughout Germany Austria or Switzerland.
Competitive salary and benefits package.
If you are located in Austria: Monthly gross salary is starting at 3.600 EUR basic - an overpay according to skills and working experience is possible. The monthly gross salary in all other countries will be different to this.

We invite you to join IQVIA!

Please apply with your English CV motivation letter and education certificates and job reference letter.

Required Experience:

Key Skills

Office Manager Experience
Microsoft Office
Customer Service
Computer Skills
Microsoft Outlook
Microsoft Word
QuickBooks
Medical office experience
Office Experience
Front Desk
Microsoft Excel
Administrative Experience

Apply Now

About Company

IQVIA

IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more

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