Clinical Trial Project Manager - REMAP-CAP Study

Are you an ambitious Clinical Trial Project Manager who likes to work on European projects? If so, we are looking for a keen and talented project manager, who can help coordinate and implement clinical trials.

About Ecraid

At Ecraid, we are committed to advancing clinical research in the field of infectious diseases by establishing a long-term, financially self-sustainable, clinical research network in Europe. Our mission is to join forces and collaborate to efficiently deliver high impact studies. Headquartered in Utrecht, the Netherlands, Ecraid is the first network of its kind in Europe to offer a single point of access to a pan-European clinical research network for infectious diseases that spans over 1,250 clinical sites and 900 laboratories across 42 countries.

The role

As a Clinical Trial Project Manager, you will play a pivotal role in the successful planning, execution, and delivery of clinical trials within Ecraid’s growing European research network. You are the central point of coordination between investigators, clinical sites, vendors, sponsors, and internal teams, ensuring that all study activities are conducted according to the highest scientific and ethical standards.

This position specifically concerns the REMAP-CAP study and is offered through a UMC Utrecht (UMCU) employment contract with direct secondment to Ecraid.

In this role, you will:

• Oversee the full operational lifecycle of clinical trials, from protocol development and site selection to database lock and final reporting.

• Develop and maintain detailed project plans, timelines, and budgets, proactively identifying potential risks and implementing mitigation strategies to ensure milestones are met.

• Serve as the main contact for sponsors and stakeholders, providing regular progress updates, performance metrics, and strategic input to enhance study efficiency and quality.

• Coordinate the work of cross-functional teams (including clinical operations, data management, pharmacovigilance, and quality assurance) to ensure seamless trial delivery.

• Monitor adherence to ICH-GCP guidelines, SOPs, and applicable (inter)national regulations, fostering a culture of continuous quality improvement “audit ready at all times.”

• Contribute to the continuous optimization of Ecraid’s operational framework, bringing forward innovative ideas to streamline processes and strengthen collaboration within our pan-European network.

This position offers the opportunity to work on impactful, high-quality research that addresses some of the most urgent challenges in infectious diseases. You will be part of an international, mission-driven organization where scientific excellence, teamwork, and purpose come together to make a difference in public health.

Requirements

To succeed in this role, the following knowledge, skills and experience are required:

·        You have at least three to five years’ experience as a clinical project manager in which you have completed all phases in the life-cycle of a clinical trial

·        HBO/ Master Degree towards Life sciences and/or biomedical sciences

·        Experience in scientific clinical research

·        Knowledge of (inter)national laws and regulations, ICH and GCP

·        Use of applications (such as EDC tools)

·        Excellent communication skills in English

·        Lives in or near the area of Utrecht, Netherlands

Next to this you are an enthusiastic, results-driven, decisive, and bright. You are quick to understand various research designs, you thrive in a fast-changing environment, and you find it rewarding to work in an international setting.

Join the movement

We offer a challenging and meaningful job in a purpose-driven work environment. Based in Utrecht, you will be surrounded by collaborative and enthusiastic colleagues. This position is offered on a temporary one-year employment contract with potential for extension. We offer a monthly gross salary of between € 4.818, - and € 6.924, - that commensurate with experience and based on a full-time 36-hour workweek.

Interested in joining our mission?

Send us your resume together with your cover letter by pressing the apply button.

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** Please note that solicitations from recruitment agencies will not be entertained.