Instagram
youtube
Facebook

Regulatory Consultant (Eu Market Experience)

3+ years
Not Disclosed
10 Feb. 4, 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

Regulatory Consultant (EU Market Experience)

Location: Gurugram, India
Job ID: 25001352
Posted: January 28, 2025

Job Description:

Syneos Health is seeking a Regulatory Consultant with experience in the EU market. This role involves managing regulatory activities for product submissions, including IND, PMA, NDA, MAA, CTD, and other regulatory agency submissions. The consultant will also contribute to the preparation of product development plans, participate in multidisciplinary teams, and ensure compliance with global regulatory requirements.

Key Responsibilities:

  • Conduct research on global/regional regulatory requirements for gap analyses and product development.
  • Prepare administrative and technical components for regulatory submissions, including IND and product registration applications.
  • Support regulatory agency interactions and contribute to briefing packages.
  • Manage day-to-day regulatory activities, ensuring timelines and scope are met.
  • Provide subject matter expertise and troubleshooting support to project teams.
  • Prepare estimates for regulatory services and support client meetings.
  • Ensure compliance with global regulatory requirements and internal processes.
  • Prepare training materials and participate in internal/external project audits.
  • Contribute to the creation and maintenance of SOPs and other process documentation.
  • Provide oversight and guidance to team members as needed.

Qualifications:

  • Minimum of 3 years of CMC module 3 experience for the EU market.
  • BS or PhD in a science-related field or equivalent experience in science, regulatory, or medical writing.
  • Experience with regulatory submissions such as IND, PMA, NDA, MAA, CTD, including electronic submissions.
  • Excellent interpersonal, communication, and customer service skills.
  • Strong analytical skills and attention to detail.
  • Proficiency in Microsoft Office applications.
  • Fluent in speaking, writing, and reading English.

About Syneos Health:

Syneos Health is a leading biopharmaceutical solutions organization, accelerating customer success by addressing modern market realities in clinical, medical affairs, and commercial insights.