Clinical Testing – Open Application
What is offered?
Are you passionate about Clinical Testing in the life sciences sector? At MindCapture we are always looking for talented individuals, from recent graduates eager to start their career to experienced professionals, who can contribute to high quality, compliant and timely clinical studies. Whether your expertise lies in study design, patient recruitment, clinical operations, medical writing, data management or drug safety, we would like to hear from you.
By joining our network you will have the opportunity to work on projects that:
- Design and execute clinical trials across all phases
- Deliver high-quality documentation that meets regulatory standards
- Manage study sites, timelines and operational workflows
- Ensure patient safety and data integrity throughout the study
- Support global regulatory submissions and inspection readiness
Job description
As a Clinical Testing professional in our network, you may contribute to projects such as:
Clinical trial design and operations
Plan and manage studies from protocol development to site selection, patient enrolment, monitoring and trial close out.
Medical writing
Produce clear and compliant protocols, investigator brochures, clinical study reports and submission dossiers that meet both scientific and regulatory requirements.
Data management
Design, implement and maintain clinical databases, ensuring clean and validated datasets that are ready for analysis and submission.
Clinical quality management
Support quality assurance activities, including SOP development, audit preparation, CAPA tracking and vendor oversight, in alignment with GCP and ICH standards.
Pharmacology and drug safety
Perform pharmacovigilance activities such as case processing, signal detection, literature review and safety reporting to protect patient wellbeing and maintain compliance.
Required competences & skills
- Degree in Life Sciences, Pharmacy, Nursing or related field (recent graduates welcome)
- Experience in clinical research within pharmaceutical, biotech or medical device environments is an advantage
- Knowledge of GCP, ICH and relevant regulatory frameworks is a plus
- Strong organisational and project management skills
- Ability to work collaboratively with sponsors, CROs and site teams
- Excellent written and verbal communication skills
- Proficiency in English, Dutch and French are an advantage
- Strong attention to detail and commitment to data quality
- Problem-solving mindset with adaptability to different study phases
- Experience with clinical trial management systems or EDC platforms is a plus
About this open application
This is not a vacancy for one specific role. It is an open invitation for Clinical Testing professionals, whether you are an experienced specialist or a motivated young graduate, to be considered for future projects and opportunities. By submitting your CV, we can match you with clients who value your skills in running reliable, compliant and patient-focused clinical studies.
Job Contact
Silke – Talent & Business Manager
Silke combines a deep understanding of our clients’ needs with a sharp eye for talent. She’s here to answer your questions, provide context about the role and support you in taking the next step in your career.
How our application process works
- Apply Online – Submit your application in just a few clicks.
- Personal interview – Our team connects with you to discuss your skills, ambitions and what you’re looking for in your next challenge.
- Client Introduction – We match you with potential projects and introduce you to clients where your expertise fits best.
- Client interview & feedback – You meet with the client to explore the project details and expectations.
- Final interview & welcome – A final chat with our management team wraps up the process, and if it’s a match, we’re excited to welcome you to MindCapture!
Explore other jobs in Clinical Testing
Jobs
Clinical Testing – Open Application
- Clinical Testing
- Flanders
- Medior
- Consultant at MindCapture
- Plan, monitor and close out clinical studies across all phases
- Safeguard patient safety and ensure data integrity
- Collaborate with teams to meet GCP and regulatory standards
Didn’t find the right match yet?
We know timing is everything. If you don’t see a role that fits you right now, we still want to hear from you. Our consultants are always looking for talent, sometimes before the job even goes live.
Drop us your CV and we’ll keep you in mind for future opportunities.
