A global headhunting team supporting the Life Science industry across the UK, EU, USA.
trials • consulting • health economics • market access • clinicalresearch
11 - 50
March 19
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A global headhunting team supporting the Life Science industry across the UK, EU, USA.
trials • consulting • health economics • market access • clinicalresearch
11 - 50
• Assist in the development and tracking of project timelines and deliverables • Coordinate and manage study documentation, including protocols, informed consent forms, and study manuals • Collaborate with cross-functional teams to ensure study milestones are met • Conduct data review and resolve data queries • Assist in the preparation of regulatory submissions • Contribute to the development of study budgets and monitor expenses
• Bachelor's degree in a scientific or healthcare-related field • +5 years of Clinical Research experience is required. • Knowledge of ICH-GCP guidelines and regulatory requirements • Strong organizational and time management skills • Excellent attention to detail • Effective communication and interpersonal skills • Proficient in Microsoft Office suite
• Fantastic work-life balance. • Competitive salary package.
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