Patient & Site Engagement Operations Manager – Sponsor Dedicated

🕒 June 30

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

⚙️ Operations

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Collaborate with pre and post award stakeholders to manage the coordination, planning, quality and implementation of Patient Recruitment and Retention operational plans on small/mid size studies. • Communicate with sponsors and project teams to implement and monitor impact of the recruitment/retention tactical plan. • Collaborate with internal teams and external providers to deliver all appropriate tactics associated with the recruitment/retention strategy. • Represent IQVIA Patient Recruitment at site/sponsor-facing meetings to present strategy/rationale, train CRAs and site staff, and conduct recruitment support workshops as required. • Ownership for study KPI and financial performance. • Manage the scope of work, objectives, quality of deliverables, and other activities of assigned projects. • Serve as primary operational project contact for patient recruitment and retention programs with sponsor. • Management of assigned project budget(s) to meet financial and company goals. • Develop and implement risk management plans.

🎯 Requirements

• Bachelor's Degree in Health care or other scientific discipline or educational equivalent • 6 yrs. of relevant industry experience • In depth knowledge of the drug development processes across all functional areas • Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines • Excellent organizational and problem solving skills • Effective time management skills and ability to manage competing priorities • Strong interpersonal skills and effective presentation skills • Ability to establish and maintain effective working relationships with coworkers, managers and clients • Computer skills including proficiency in aspects of data analysis and presentation software, Microsoft Word, and Excel • Good written and verbal communication skills including good command of English • Ability to influence effectively within SPN/PRP team and project teams including TSL, PL, CL, CRA and the customer.

🏖️ Benefits

• Professional development • Possibility to work from any EMEA country as long as the time zone is no more than six hours ahead of US Eastern Time. • Opportunities to participate in congress/conference planning for R&D activities. • Ability to work collaboratively with global teams.