Regulatory Associate – AdPromo

🕒 June 30

🌐 Argentina, Brazil, +1 more countries – Remote

🇦🇷 Argentina – Remote 🇧🇷 Brazil – Remote 🇲🇽 Mexico – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🚔 Compliance

👻 Ghost score 65%

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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Syneos Health

WebsiteLinkedInAll Job Openings

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

• Build and institutionalize regulatory project management frameworks, tools, and best practices to enhance GRA-AP capability and effectiveness • Provide strategic oversight of GRA-AP projects and portfolios, ensuring alignment with objectives and timelines • Coordinate and facilitate communication among regulatory affairs, project teams, stakeholders, knowledge management, and external partners • Track project progress, materials, and deliverables • Proactively identify and resolve issues to maintain project momentum • Lead and participate in regulatory project meetings • Document meeting minutes, update project portals, and communicate outcomes to stakeholders • Perform administrative functions supporting project teams and department operations

🎯 Requirements

• Bachelor’s degree in a scientific discipline, clinical, regulatory affairs, project management, or a related field • Minimum of 3 years’ experience in regulatory project management within the pharmaceutical or biotechnology industry, or an equivalent combination of education and experience • Demonstrated ability to build project management frameworks, explain procedures, and implement identified team initiatives • Excellent written and verbal communication skills • Proven stakeholder engagement, strong briefing, and influencing skills • Strong organizational, analytical, and problem-solving skills • Focus on continuous improvement • Proficient in project and knowledge management software and techniques • Advanced computer skills supporting and maintaining department software, including Microsoft platform, OneDrive, and SharePoint • Ability to work independently and under moderate supervision • Ability to manage competing priorities across several projects • Regulatory platforms such as Veeva preferred but not required

🏖️ 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, under the Americans with Disabilities Act