Manager, Regulatory Affairs – EMEA

🕒 September 21

🌐 Romania, France, +5 more countries – Remote

🇷🇴 Romania – Remote 🇫🇷 France – Remote 🇭🇷 Croatia – Remote 🇪🇸 Spain – Remote 🇬🇧 United Kingdom – Remote 🇷🇸 Serbia – Remote 🇵🇱 Poland – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🚔 Compliance

👻 Ghost score 10%

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

• Review study budgets and costing related to contract negotiation • Participate in business development activities • Prepare regulatory sections of proposals and feasibility reports • Attend bid defense meetings • Coordinate and manage regulatory and ethics committee submissions across EMEA, Asia Pacific, and Latin America • Maintain approvals and ensure accurate compilation, management, and tracking of submissions • Provide expert regulatory advice and contribute to regulatory project work • Communicate submission status with Sponsors, Project Managers, CRAs, and Medical & Scientific Affairs staff • Contribute to technical documentation such as IMPDs and IBs • Review documentation and make recommendations to ensure compliance with ICH GCP and country-specific requirements • Provide training, coaching, and mentoring to junior staff • May line manage junior staff

🎯 Requirements

• Clearly proven leadership and organizational management skills • Strong planning, strategizing, managing, monitoring, scheduling, and critiquing skills • Excellent written and verbal communication skills • Relationship-building competency and comfort supporting Business Development at face-to-face meetings • Strong interpersonal skills in a fast-paced, deadline-oriented, changing environment • Ability to handle multiple tasks in a fast-paced and constantly changing environment • Minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy, or another related science; OR two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree) and eight years of experience within clinical research • Minimum 5–7 years within the pharmaceutical/CRO industry, with demonstrated senior-level regulatory or clinical start-up experience • Proficiency in cross-cultural communication • Proficiency in spoken and written English

🏖️ Benefits

• Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law • Supportive and cohesive teams • Diverse and inclusive workplace • Opportunities for training, coaching, mentoring, and professional development