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Senior clinical research specialist

Machelen (Flandre Orientale)
Pauwels Consulting
Publiée le 18 février
Description de l'offre

Join a pioneering MedTech environment where your expertise will contribute to the advancement of transformative clinical studies. Our client is searching for a dedicated professional eager to advance their career as a Senior Clinical Research Specialist.
As a successful candidate, you are an experienced Senior Clinical Research Specialist who is passionate about clinical trials and thrives in a collaborative environment. If you are proactive, detail-oriented, and ready to take on significant responsibilities, we invite you to be part of our dynamic team.
You support the execution of company-sponsored clinical trials ensuring compliance with timelines and study milestones.
You oversee and execute feasibility, selection, set up, conduct, and closure of clinical trials according to ICH-GCP standards.
You may serve as the primary contact for clinical trial sites, facilitating site management.
You contribute to the development of critical clinical trial documents, including protocols and consent forms.
You manage ordering, tracking, and accountability of investigational devices and trial materials.
You mentor team members and act as a reliable resource for project knowledge.
You support project budget activities and ensure adherence to safety and compliance regulations.
What are we looking for?
You hold a Bachelor's degree preferably in Life Science, Physical Science, Nursing, or Biological Science.
You have a minimum of 4 years of experience in clinical research (a master's degree may reduce this requirement).
You possess relevant industry certifications (e.g., CCRA, CCRC, CRP) and concepts related to clinical research.
You bring strong analytical and problem-solving capabilities.
You are an excellent communicator, with a strong ability to collaborate in a team environment.
You demonstrate flexibility, proactiveness, and assertiveness in managing workload.
You are willing to travel approximately 20% of the time as required.
You are fluent in English, with proficiency in any other European language being an advantage.
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