Join our amazing team and share with our journey

Founded in 1997, our commitment and obligation to Clinical Trials have been set in

stone: Make each study a success.


For more than 24 years S-Clinica has been driven by a dynamic adoption of

scientifically proved practices. As a result, S-Clinica excels in providing fully

integrated & customizable solutions.


We provide immediate support and meticulous attention to every project from beginning to end, and we build long-term partnerships with each client and each client’s team.

We are proud to say that we are the preferred provider of our very first client, a Top-5 Pharma-Biotech Company. This partnership has resulted in 24 years of successful collaboration!

A key element of our success is our team. 

See our openings below


Clinical Trial RTSM Project Manager

Posted 12th August 2021

Location: Brussels/Belgium

S-Clinica is one of the world’s leading clinical technology companies offering services to pharmaceutical and biotechnology firms conducting clinical trials. Our integrated RTSM solution (Supply Forecasting, IWRS, Drug Supply Management, ePRO) supports the services we provide. We pride ourselves on the quality of our products, our dedication to teamwork, and our commitment to success. We are pleased to expand S-Clinica’s team and offer intelligent, motivated, and dedicated professionals to join our global operational team.

As RTSM Project Manager, you will be responsible for all RTSM project aspects. You will act as a key contact person for the client, helping to manage study timelines and scope. You will analyze project requirements, prepare system specifications and participate in system setup. You will manage the project once the system is live. By using S-Clinica’s tool, you help the client to analyze the drug supply needs of the project.

Job Description


  • Manage RTSM and Drug Supply Management projects

  • Commit to quality services: be pro-active and ensure the successful development of the project, be attentive to detail, anticipate issues, and drive prompt resolutions

  • Act as primary contact for the client and for the internal team; ensure fluid communication between project participants and lead project meetings

  • Participate in system setup including but not limited to analyses of project requirements, system design, and setup, management of timelines, the scope of work, development of documentation

  • Work in compliance with internal procedures and requirements

  • Prepare and assist at client’s User Acceptance Test

  • Act as a Level 2 Helpdesk support

  • Coordinate management and documentation of incidents and problems

  • Control drug supply (monitor risks, anticipate shortage)

  • Be professional in the accomplishment of individual and team objectives and contribute to the positive teamwork environment

Job Requirements

  • Bachelor's degree; experience in project management in clinical trials is a plus

  • Strong analytical, organizational, communication, and presentation skills

  • Knowledge of clinical trial systems and experience is a plus

  • Responsible, pro-active, positive, and dedicated to success

  • Able to manage multiple timelines and to work in a fast-paced environment

  • Team-oriented but autonomous

  • Ability to learn quickly, attentive to details, proactive and positive

  • Be willing to provide at any time on-call technical support for own or backup projects

We Offer

  • Competitive salary

  • Dynamic and enthusiastic company

  • Career growth opportunities

For more information or to send your CV, please write to