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Senior Associate - Ra (Northern Cluster)

Clinchoice
ClinChoice
3-5 years
Not Disclosed
10 Nov. 4, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

Position: Senior Associate – Regulatory Affairs (Northern Cluster)

Location: Bengaluru, India


Job Summary:

The Senior Associate – Regulatory Affairs (Northern Cluster) will support regulatory operations for products across the UK, Ireland, Malta, Sweden, Finland, Norway, and Denmark. The role involves preparing and managing regulatory submissions, ensuring compliance with European and national regulatory requirements, and supporting lifecycle management and Pharmacovigilance-related activities. The position requires close collaboration with cross-functional teams and regulatory authorities to maintain the quality and compliance of the product portfolio.


Key Responsibilities:

Regulatory Strategy & Submissions

  • Support the Northern Cluster team in developing and executing local and regional regulatory strategies aligned with the business plan.

  • Prepare, compile, and review regulatory submissions for National and European procedures (Decentralized, Mutual Recognition).

  • Manage renewals, variations, and post-approval updates including maintenance of external regulatory websites (e.g., emc, medicines.ie, In-Demand).

  • Support ad hoc regulatory projects, such as compliance reviews and audit preparations.

  • Review and sign off on packaging materials, leaflets, and SmPCs where applicable.

Compliance & Documentation

  • Ensure adherence to global and regional SOPs, processes, and work instructions.

  • Maintain and update global and local regulatory databases (e.g., Documentum, Aris, Connect) to track product information accurately.

  • Support compilation and submission of Northern Cluster team metrics for EMEA biannual regulatory reports.

  • Ensure compliance with internal quality standards and regulatory obligations in all assigned markets.

Pharmacovigilance & Communication Support

  • Assist in responding to Calls for Information (CFIs) and related Pharmacovigilance activities in coordination with UK and EAME colleagues.

  • Monitor and ensure timely submission of responses to CFIs in accordance with established procedures and metrics.

  • Provide regulatory support to the UK PV group and address queries from the Global Regulatory Medical mailbox.

Cross-functional Collaboration

  • Collaborate effectively with internal teams across Regulatory Affairs, Quality, and Pharmacovigilance functions.

  • Support all regulatory activities related to the Malta market.

  • Contribute to the coordination of compliance initiatives and continuous process improvement within the Northern Cluster team.


Qualifications & Experience:

Education:

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related field.

Experience:

  • 3–5 years of relevant experience in Regulatory Affairs within the pharmaceutical, cosmetic, or food supplement industry.

  • Hands-on experience in CMC, Quality, or Regulatory Operations preferred.

  • Direct accountability for regulatory deliverables and timelines.

Core Competencies:

  • Strong understanding of European regulatory frameworks (Decentralized and Mutual Recognition Procedures).

  • Excellent project management and communication skills.

  • Proficiency in maintaining regulatory databases and documentation systems.

  • Ability to work independently while collaborating across global teams.

  • Attention to detail, organizational discipline, and a compliance-oriented mindset.