Director, Regulatory Pre-Award Strategy

🕒 June 5

🌐 United Kingdom, Canada, +2 more countries – Remote

🇬🇧 United Kingdom – Remote 🇨🇦 Canada – Remote 🇪🇸 Spain – Remote 🇭🇷 Croatia – Remote

⏰ Full Time

🔴 Lead

🚔 Compliance

🇬🇧 UK Skilled Worker Visa Sponsor

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

👻 Ghost score 36%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Accountable for senior-level leadership in establishing operational strategy for global regulatory affairs. • Oversees delivery and performance of regulatory affairs activities. • Provides expert regulatory advice and contributes to project work for internal and external customers. • Responsible for planning and oversight of regulatory affairs activities, ensuring high quality and timely delivery. • Engages in business development activities by contributing to proposals and bid defense meetings. • Stays informed about changing regulatory affairs requirements and ensures team training. • Responsible for submission/approval of regulatory dossiers and maintaining compliance with regulations.

🎯 Requirements

• A minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy or other related science, OR… • Two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and eight years’ experience within clinical research (e.g. CRA, Reg Affairs.) • Minimum 10 years within pharmaceutical/CRO industry, with demonstrated senior level regulatory or clinical start-up experience • Proficient in cross-cultural communication and proficient in both spoken and written English.

🏖️ Benefits

• Competitive salary • Flexible working hours • Professional development opportunities • Inclusive workplace culture