Job Location: DIEGEM

Project Manager YTP

  • Location: Diegem
  • Remote: Remote
  • Type: Contracting
  • Job #27841

Junior IT Project Manager (Graduate Opportunity)

 

📍 Diegem, Belgium

🎓 Recent Graduates Welcome (Bachelor's or Master's Degree)

💼 Full-time | Permanent Contract

🚀 Training & Mentoring Program Included

 

Kick-Start Your Career in IT Project Management !

Have you recently graduated and are looking for an opportunity to combine technology, business, and project management?

We are looking for a Junior IT Project Manager to join our client's team and contribute to exciting digital transformation, application development, systems integration, AI- implementations and many more projects !

Our client is an international and forward-thinking company at the forefront of digital innovation. Working on transformative projects involving cloud, AI, applications, and digital platforms, they empower young talent to create meaningful impact and build the technologies of tomorrow.

This role is designed for ambitious young professionals eager to learn, grow, and build a successful career in the world of IT project management.

 

What You Will Do

 

As a Junior IT Project Manager, you will:

  • Support the planning and delivery of IT and digital projects
  • Coordinate project activities and ensure deadlines are met
  • Work closely with business stakeholders, technical teams, and vendors
  • Organize project meetings and follow up on action items
  • Track project progress, risks, and issues
  • Assist with project documentation and reporting
  • Learn and apply Agile, Scrum, and Waterfall methodologies
  • Contribute to process improvement and digital transformation initiatives

 

Who We Are Looking For

 

  • You recently obtained (or are about to obtain) a Bachelor's or Master's degree in IT and/or Management field(s).
  • Strong interest in technology and digital innovation
  • Excellent communication and interpersonal skills
  • Organized and detail-oriented mindset
  • Strong analytical and problem-solving abilities
  • Eager to learn and take ownership
  • Team player with a proactive attitude
  • Fluent in English and Dutch ; French is a plus

 

Why Join them ?

 

✅ Structured onboarding and tailor-made mentoring program.

✅ Hands-on experience on real IT projects

✅ Continuous learning and professional development leading to fast career growth opportunities.

✅ Exposure to Agile project management practices

✅ Collaborative and supportive team environment

✅ Competitive salary and benefits package (including company car)

✅ Opportunity to obtain the NATO clearance : highly valued credential that opens doors to exclusive opportunities within international institutions, defence programs, and mission-critical IT projects.

 

Ready to Launch Your Career?

Whether you have previous internship experience or are taking your first step into the professional world, we would love to hear from you.

 

If this sounds interesting, feel free to reach out : [email protected]

Clinical Research Associate (CRA)

  • Location: diegem
  • Type: Contracting
  • Job #26563

CRA

Contracting – Antwerpen
 

Tasks

  • Ensure the safety and well-being of study subjects at assigned clinical sites.
  • Support the operational execution of clinical trials and ensure high-quality data collection.
  • Perform trial activities in compliance with SOPs, GCP, and applicable regulatory requirements.
  • Be accountable for site performance and delivery of high-quality data within project timelines.
  • Assist Clinical Operations staff and site personnel to resolve issues and implement CAPAs when needed.
  • Verify that Investigator Site Files are maintained according to regulations and company procedures.
  • Support patient recruitment and retention activities.
  • Conduct site visits to ensure compliance with protocol and regulations.
  • Contribute to the internal communication of important clinical data and events.
  • Support the organization of Investigator meetings and study trainings.
  • Serve as a reliable resource for up-to-date site status knowledge for stakeholders.
  • Assist in the implementation of new clinical systems and processes.
  • Collaborate with Investigators, IRBs/ECs, vendors, and internal staff.
  • Comply with all applicable laws, regulations, and company compliance policies.

 

Profile

  • Bachelor’s Master’s , PhD in Life Sciences, Physical Sciences, Nursing, or Biological Sciences required.
  • Fluency in English, French and Dutch.
  • Previous clinical research experience required.
  • Experience in medical device monitoring (or equivalent) required.
  • Solid understanding of regulations and standards in clinical research and medical devices/combination products.
  • Relevant industry certifications (e.g., CCRA, RAC, CDE) are an asset.
  • Clinical/medical background is a plus.
  • Proficiency in Microsoft Office (Excel, Word, PowerPoint).

 

Our offer?

Jefferson Wells offers you a permanent contract as consultant with an attractive salary package and will give you access to trainings in technical matters and soft skills. We will be your career partner for each step along the way. You’re interested in this job? We kindly invite you to apply or send me your CV, [email protected]