here are the perks: Hybrid (2 days in office), providing flexibility when able Free parking onsite 25 days holiday per annum + recognised bank holidays You will be the kind of person who wants to make a difference within your day-to-day work, but of course there are
a few other requirements: Customer-Centricity:
Prioritise patient and site needs, fostering a customer-focused culture that drives growth and innovation. Growth Mindset:
Embrace learning, encourage others to do the same, and take on new experiences and risks. Enterprise View:
Advocate for the broader organizational goals, understanding trade-offs and resource impacts. Diversity, Equity & Inclusion:
Promote a diverse and inclusive environment, ensuring all voices are heard and valued. Organisational & Problem-Solving Skills:
Efficiently plan and manage clinical operations programs. Communication:
Transparent, strategic, and effective in both speaking and listening. Leadership:
Inspire and collaborate with diverse teams. You will also be
responsible for: Ensuring the seamless execution of all operational aspects of one or more studies across all phases (start-up, conduct, and closeout), in compliance with ICH / GCP and relevant regulatory standards. Developing and monitoring study timelines, budgets, risks, and operational plans, ensuring quality and compliance, while incorporating diversity and inclusion strategies as applicable. Managing the selection, oversight, and closure of study-related vendors, ensuring smooth operations, tracking budgets, and approving related invoices. Overseeing country-specific study operations, collaborating with country COLs and third-party CROs (when applicable) to ensure effective and efficient study implementation. Serving as the primary point of contact for country COLs, providing oversight of study performance, addressing issues, and coordinating corrective actions as needed. Collaborating with global and local teams to respond to regulatory inquiries and audits from IRBs, Health Authorities, and Ethics Committees, ensuring adherence to best practices and consistent study execution. Facilitating communication with stakeholders through various channels (calls, newsletters, etc.), keeping them informed of study progress, timelines, risks, and operational plans, ensuring alignment across regions. May work with the Global Patient Partner to incorporate the patient's voice and perspective into the study strategy. Ensuring the timely distribution of key study documents (protocols, ICFs, manuals) to country COLs. Potentially developing and implementing a study-specific diversity plan. If you are interested in this excellent Global Clinical Operations Lead role, please apply here or get in touch with Chloe Mccausland at Clearline Recruitment. Job Title:
Global Clinical Operations Lead Location:
Welwyn (Hybrid - 2 days minimum in office) Salary:
.97 per day (PAYE) OR .00 per day (UMB) Full Time:
37.5 hours per week 6 Month Contract (Inside IR35)
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