Regulatory Strategist – International, Manager

🔥 12 hours ago

🇨🇱 Chile – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🚔 Compliance

👻 Ghost score 10%

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Logo of Syneos Health

Syneos Health

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Lead and support submissions in Latin American markets for MAAs and life-cycle management procedures • Provide local expertise as a member of the Global Regulatory Affairs team • Drive and coordinate regulatory strategy and local regulatory activities in Latin America • Provide regional regulatory expertise for geographical expansion • Track Health Authorities’ requests and relevant new local regulations • Maintain current knowledge of local requirements and communicate regulatory changes to senior management • Lead cross-functional Vertex teams through submission planning, preparation, submission, and review • Prepare responses to regulatory questions • Prepare timelines and create submission binders in Veeva • Keep submission and correspondence files up to date • Act as local expert for regulatory queries from medical, supply chain, and other functions • Ensure work complies with regulatory requirements and company policies and procedures

🎯 Requirements

• Relevant industry experience in regulatory affairs in Latin America • Understanding of current trends in local and regional requirements • Knowledgeable resource for regulatory advice by other departments • Experience interacting with Regulatory Authorities • Ability to facilitate interactions with International Regulatory Affairs, other departments within the Company, and external parties, mainly submission partners • Bachelor’s degree in Pharmaceutical Sciences • Advanced written and spoken English • Knowledge of Spanish and Portuguese considered an advantage

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Reasonable accommodations when appropriate

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