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Regulatory Consultant (Eu Market Experience)

3+ years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: BS/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

πŸ“Œ Regulatory Consultant (EU Market Experience) | Syneos Health
πŸ“ Location: Home-Based (India-Asia Pacific)
πŸš€ Leading Biopharmaceutical Solutions Organization

🌟 About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization, designed to accelerate customer success by providing unique insights across clinical, medical affairs, and commercial sectors. We are committed to simplifying and streamlining processes, ensuring that we are the partner you can count on.

πŸ“ About the Role

As a Regulatory Consultant, your primary focus will be managing and contributing to regulatory submissions for the EU market, ensuring compliance, and offering expertise across all stages of product development. Your contributions will directly impact the successful delivery of innovative therapies.

πŸ” Key Responsibilities

βœ” Regulatory Submissions: Manage and contribute to IND, PMA, NDA, MAA, and CTD submissions.
βœ” Product Development & Compliance: Conduct gap analyses, prepare development plans, and contribute to regulatory activities in the EU market.
βœ” Team Support: Collaborate with multidisciplinary teams to support product lifecycle activities and troubleshoot project-related issues.
βœ” Client & Proposal Support: Assist in preparing proposals, conducting client meetings, and discussing ongoing project statuses.
βœ” Regulatory & Quality Assurance: Ensure compliance with global regulatory standards, and participate in audits and process documentation development.
βœ” Training & Best Practices: Create training materials and share best practices across regulatory processes internally and externally.

πŸ“‹ Qualifications

πŸŽ“ BS or PhD in a science-related field or equivalent regulatory/medical writing experience.
πŸ“Œ Minimum 3 years of experience in CMC module 3 for the EU market.
πŸ“Œ Proven experience in preparing and contributing to regulatory submissions (IND, PMA, NDA, MAA, CTD).
πŸ“Œ Excellent communication and customer service skills, both written and verbal.
πŸ“Œ Proficiency in Microsoft Office and regulatory management tools.
πŸ“Œ Strong analytical, organizational, and problem-solving skills.
πŸ“Œ Fluency in English (both written and spoken).

🌍 Why Syneos Health?

🌟 Career Growth: Advance your career through training, recognition, and progression opportunities.
🌍 Diversity & Inclusion: Be part of a team that celebrates diverse thoughts, cultures, and perspectives.
πŸ’Ό Impact: Work on groundbreaking projects and contribute to 94% of FDA-approved drugs over the past 5 years.

πŸ“© Apply Now