Offer summary

Qualifications:

At least 5 years of experience in RBQM-focused clinical research., Strong analytical skills with attention to detail in data interpretation., In-depth understanding of clinical trial processes and RBQM requirements., Excellent verbal and written communication skills for client interactions..

Key responsibilities:

Lead consultations with clients to conduct risk assessments and provide recommendations.

Review client protocols and implement RBQM best practices.

Collaborate with internal teams to shape product development aligned with RBQM standards.

Create educational materials to support clients in their RBQM journey.

Job description

Job Description

We are a rapidly expanding, innovation-driven company in the e-clinical space, setting new standards in data quality and patient safety for clinical trials. Our cutting-edge, AI-powered solutions empower our clients—leading pharmaceutical companies and CROs worldwide—to integrate Risk-Based Quality Management (RBQM) practices seamlessly, optimizing trial outcomes while maintaining compliance with industry standards.

The Opportunity:

Are you a seasoned RBQM specialist with hands-on experience in clinical risk management?

We’re looking for an RBQM Expert to deliver high-impact guidance and expertise, helping our clients implement and enhance RBQM processes tailored to their specific needs. This role is an opportunity to influence the future of clinical research by applying your RBQM skills in consultations, protocol reviews, and practical, client-centered training.

If you’re passionate about advancing RBQM and driving real change in the clinical field, this is the role for you!

*This position can be remote from the US, Belgium, United Kingdom or Poland*Job Requirements

RBQM Expertise: At least 5 years of experience in RBQM-focused clinical research, with proven skills in risk assessments, critical-to-quality identification, and data-driven risk management.
Analytical Precision: A sharp eye for detail with a strong analytical approach to interpreting data and managing risks.
Industry Knowledge: In-depth understanding of clinical trial processes, study phases, and RBQM requirements across therapeutic areas.
Collaborative Communication: Excellent verbal and written communication skills for both internal and client interactions.
Driven by Impact: Comfortable in a high-growth, innovative environment where your expertise will have a tangible impact on the future of clinical research.

Job Responsibilities

Deliver Expert RBQM Consultation: Lead detailed consultations with clients, conducting risk assessments and offering data-driven recommendations that enhance trial quality.
Guide Protocol and Process Improvement: Provide technical insight in reviewing client protocols and implementing RBQM best practices across studies.
Collaborate on Product Development: Work closely with internal teams to provide feedback that shapes our products and ensures alignment with RBQM standards.
Develop Educational Resources: Create materials and tools that support clients in their RBQM journey, reinforcing industry-leading practices.

Job Benefits

Innovative Culture: Work at the forefront of e-clinical solutions, helping shape the industry’s approach to data quality and patient safety.
Expert Community: Join a team of highly skilled professionals who value collaboration, growth, and expertise.
Meaningful Work: Drive real improvements in clinical trial outcomes, supporting clients in adopting industry-leading RBQM practices.

Ready to Make an Impact?

If you’re a dedicated RBQM specialist ready to elevate the future of clinical research, we’d love to hear from you! Apply today to be part of a team that’s transforming RBQM in the pharmaceutical industry.

Required profile