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Regulatory Affairs Consultant (Biologics)

8-9 years
Not Disclosed
10 Nov. 30, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Role: Regulatory Affairs Consultant - Parexel Consulting

As a Regulatory Affairs Consultant with Parexel Consulting, you will leverage your scientific, technical, and regulatory expertise to guide biopharmaceutical and medical device companies through the dynamic regulatory environment. You will collaborate with clients to streamline regulatory processes, ensuring faster product approvals and sustainable compliance. This role offers an opportunity to develop innovative regulatory strategies for diverse product types and therapeutic areas while enjoying remote work flexibility.


Key Responsibilities

Regulatory Lifecycle Management

  • Manage the pre- and post-approval lifecycle for biologic products in regulated markets (EU/US/Canada) and emerging markets.
  • Compile, submit, and obtain approval for country-specific submissions, including Marketing Authorization Applications (MAA), lifecycle management (LCM), and post-approval changes.
  • Author and deliver both simple and complex regulatory maintenance submissions at global and regional levels.
  • Prepare and review variations and marketing authorization applications across regulated, emerging, and EU markets.

Compliance and Regulatory Guidance

  • Stay updated on local and international regulatory guidelines and trends to ensure compliance.
  • Support affiliates by providing updates on local regulatory requirements, ensuring alignment with agency guidance.
  • Collaborate with cross-functional teams to execute submission delivery and content plans while providing proactive updates to stakeholders.

Process Management and Tools

  • Utilize Regulatory Information Management Systems (e.g., Veeva Vault) to manage and maintain submission data.
  • Develop and maintain submission delivery plans, ensuring timely execution.
  • Drive efficiency in submission processes, adapting strategies based on regulatory feedback and industry changes.

Collaboration and Communication

  • Liaise closely with cross-functional teams and stakeholders to align product responsibilities.
  • Ensure clear, consistent communication with internal teams, clients, and regulatory agencies.
  • Foster strong relationships with affiliates, distributors, and global regulatory bodies to facilitate streamlined processes.

Ideal Candidate Profile

Qualifications and Experience

  • 8-9 years of experience managing pre- and post-approval regulatory lifecycles for biologic products in regulated and emerging markets.
  • Proficiency in compiling and authoring regulatory submissions, including MAAs, variations, and LCM documentation.
  • Strong understanding of local and international regulatory frameworks and guidelines.
  • Experience with Regulatory Information Management Systems, particularly Veeva Vault.

Skills and Competencies

  • Technical Expertise: Comprehensive knowledge of regulatory procedures and submission requirements for biologics.
  • Communication: Strong ability to communicate effectively and collaborate with cross-functional teams.
  • Problem Solving: Results-driven approach to addressing regulatory challenges with innovative solutions.
  • Detail-Oriented: High level of precision in managing submissions and compliance activities.
  • Project Management: Capability to execute and maintain submission plans while meeting deadlines.

Why Join Parexel?

  • Impactful Work: Help clients navigate complex regulatory landscapes and bring life-changing products to market.
  • Continuous Growth: Gain exposure to diverse product types and therapeutic areas, with opportunities for mentorship and challenging assignments.
  • Flexible Environment: Enjoy remote work options while being part of a dynamic and supportive global team.
  • Innovative Culture: Work in a collaborative setting that values strategic thinking and results-oriented solutions.

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