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Our client is a renowned organization in the field of medical technology and clinical research, dedicated to innovation and excellence. They provide a dynamic and international work environment where personal and professional growth is encouraged.
Our client is a renowned organization in the field of medical technology and clinical research, dedicated to innovation and excellence. They provide a dynamic and international work environment where personal and professional growth is encouraged.
Randstad Professional, a leading HR services provider specializing in placing highly qualified professionals, is looking for a Clinical Research Specialist for our valued client in the MedTech sector.
...Randstad Professional, a leading HR services provider specializing in placing highly qualified professionals, is looking for a Clinical Research Specialist for our valued client in the MedTech sector.
As a Clinical Research Specialist, you will support one or more clinical studies within the Clinical R&D department, collaborating with internal and external stakeholders to ensure compliance with guidelines and achievement of study milestones.
Key Responsibilities:
Support the feasibility, initiation, conduct, and closure of clinical trials.
Act as the primary point of contact for clinical trial sites, assisting with documentation (study protocols, informed consents, monitoring plans, etc.).
Coordinate and manage investigational devices, trial materials, and budgets.
Contribute to the development of study reports and data analysis for publications.
Conduct monitoring activities, including site visits, data collection, and protocol compliance, as needed.
Collaborate with investigators, ethics committees, and vendors to ensure smooth study execution.
Provide safety coordination during clinical studies, including the reporting of safety data and adverse events.
Degree: Bachelor’s degree in Life Science, Physical Science, Nursing, or Biological Sciences (required).
Experience:
Minimum 2 years of experience in clinical research (BS-level) or 1 year (MS/PhD-level).
Relevant certifications (e.g., CCRA, CCRC, CCRP, GCP) are a plus.
Medical device experience is a strong advantage.
Skills:
Solid understanding of clinical research and regulatory guidelines.
Excellent organizational and communication skills.
Strong technical writing and presentation abilities.
Fluency in English; additional language skills are an advantage.
A market-competitive salary according to PC200.
Hospitalization insurance.
Group insurance.
32 days of leave (20 legal + 12 extra).
Meal vouchers.
Opportunities for professional development and training.
Hybrid working with travel flexibility (approximately 20%).