EPM Scientific are currently partnered with a global medical device organisation supporting the development of innovative therapies within cardiology and electrophysiology. They are urgently seeking a Senior Clinical Research Specialist, reporting to the Clinical R&D Manager, to support the execution of pre-market and post-market clinical studies across Europe and international markets. This position will play a key role in ensuring clinical studies are delivered on time, within budget, and in compliance with applicable regulations, while collaborating closely with cross-functional stakeholders and external research sites.
Role Overview:
- Start date: ASAP
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Location: Brussels, Belgium (Hybrid)
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Contract Type: Freelance / Consultant - 1 FTE, Contract until 31 December 2026
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Language: Fluent English required; additional European languages advantageous
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Project: Pre-market and post-market clinical studies in cardiology and electrophysiology
Key Responsibilities:
- Support the planning, execution, and delivery of clinical studies in accordance with ICH-GCP, applicable regulations, and company procedures.
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Manage study activities including feasibility assessments, site selection, study start-up, site management, monitoring oversight, and study close-out.
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Act as a key point of contact for investigators, study sites, vendors, ethics committees, and internal stakeholders throughout the study lifecycle.
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Contribute to the development and review of study documentation including protocols, informed consent forms, CRFs, monitoring plans, and study manuals.
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Coordinate clinical trial timelines, budgets, study materials, investigational product accountability, and trial deliverables.
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Review clinical data, support study reporting activities, and collaborate with cross-functional teams to ensure high-quality study execution and regulatory compliance.
Requirements:
- Bachelor's degree or higher in Life Sciences, Nursing, Biological Sciences, Pharmacy, or a related scientific discipline.
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Minimum 4 years of experience in clinical research within the pharmaceutical, biotechnology, CRO, or medical device industry.
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Strong knowledge of ICH-GCP, clinical trial regulations, and clinical study management processes.
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Experience coordinating international clinical studies, including site management and cross-functional stakeholder engagement.
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Medical device experience is highly desirable; experience within cardiology or electrophysiology studies is advantageous.
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Excellent project management, communication, organisational, and prioritisation skills, with flexibility to travel internationally when required.
If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.
