Clinical Operations Lead

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Biomapas

WebsiteLinkedInAll Job Openings

201 - 500 employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Biomapas is a comprehensive outsourcing solution provider catering to the global life science sector. The company acts as a strategic partner for biopharmaceutical and medical device companies, offering extensive clinical research services worldwide. Biomapas covers the entire product lifecycle from regulatory compliance to pharmacovigilance and medical information. The company operates across various regions including Europe, CIS, EAEU, MENA, LATAM, and the US, ensuring high-quality, efficient, and cost-effective methodologies to deliver superior service and strategic advantages. With a focus on clinical trials, pharmacovigilance, and regulatory affairs, Biomapas is equipped to navigate complex regulatory environments and manage clinical trial data effectively, contributing to clients' commercial success.

📋 Description

• Oversight of (a group of) study CRAs to ensure (site) compliance with study protocol, study plans, ICH-GCP, local regulations and study timelines • Monitoring support visits (Accompanied site visits), per project requirements, to aid the site/CRA in the satisfactory performance and compliance with standards • Develop training materials and study tools for sites and CRAs, including monitoring plans • Develop and implement enrolment and recruitment strategies together with clinical project team • Support clinical project team by providing oversight of study deliverables related to other functions (e.g. Data Management, TMF Operations, etc.) • Proactive management of site and country performance (recruitment, data collection, document collection, TMF review, timely update of Biomapas/sponsor CTMS by the study CRAs etc.) and inform clinical project team on progress • Oversee regional startup and feasibility activities • Provide project training/mentoring to regional CRAs on study procedures, clinical plans and guidelines, and timelines for the study • Assist in vendor management activities as required per project • Perform review of visit reports for quality, compliance and appropriate site management • Assure compliance with high quality and timely project deliverables according to the project requirements and the monitoring plan

🎯 Requirements

• Bachelor’s or Master’s Degree in Medicine, Pharmacy or Life science • 3 years experience in Clinical Lead role • Fluent written and spoken English language • Good coordination skills • Attention to detail, time-management and problem-solving skills • Strong organization and analytical skills

🏖️ Benefits

• Professional growth and career opportunities • International team and environment • Bonus based on annual performance • Personal accident and business trip insurance • Additional health insurance • Remote/home based • Complimentary health and wellness benefits, such as influenza vaccines • Rewarding referral policy • Workplace establishment allowance (fully remote) • Team building, global meetings, B active events