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Associate Manager - Regulatory Solutions

10-12 years
Not Disclosed
10 March 25, 2025
Job Description
Job Type: Full Time Education: MBBS/PhD/MDS/BDS/MPharm/PharmD 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

Associate Manager - Regulatory Solutions
Date: 19 Mar 2025
Location: Mumbai, MH, IN

We are a technology-led healthcare solutions provider. We enable healthcare organizations to be future-ready by offering accelerated global growth opportunities for bold, industrious, and nimble talent. At Indegene, you will gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy.

If you are looking for growth and variety in your career, join us in our journey and grow with us. We hire the best and trust them from day one to deliver global impact, handle teams, and be responsible for outcomes while our leaders support and mentor you.

We are a profitable and rapidly growing global organization operating at the intersection of healthcare and technology, offering global opportunities and fast-track careers with a team driven by purpose.

EDUCATION:
MBBS/PhD/MDS/BDS/MPharm/PharmD

EXPERIENCE:
10 to 12 years of experience in writing Clinical & Regulatory documents supporting global filings (CTD Module 2 and Module 5).

ROLE PURPOSE:
This role is responsible for handling complex Medical Writing projects, providing review support for medical writing deliverables that support the clinical regulatory writing portfolio, and training junior writers.

SKILLS:

  • Experience authoring a broad set of clinical document types supporting regulatory filings, with a preference for experience with Module 2.4, 2.5, 2.6, 2.7, 5.2, clinical study reports (CSRs), protocols, amendments, ICFs & amendments, and Investigator Brochures (IBs).

  • Demonstrated excellence in focused/lean writing and editing following defined processes and templates.

  • Ability to lead cross-functional teams to draft agreed-upon scientific/medical content addressing data interpretation, product claims, and internal/external queries.

  • Understanding of the clinical development process from program planning to submission, including clinical trial design.

  • Strong communication skills suited to a professional working environment.

  • Effective time management, organizational, and interpersonal skills.

  • People management experience of more than 2 years.

  • Customer focus and ability to follow directions, templates, and structured processes for document delivery.

  • Ability to work independently while maintaining communication with the Sponsor’s MW project manager.

  • Flexibility to move across Therapeutic Areas to support business continuity and resource needs.

  • Ability to develop, coordinate, and oversee work plans for document delivery, ensuring all tasks, timelines, and roles are efficiently managed.

  • Ability to facilitate review meetings, address feedback, and negotiate solutions/agreements.

KNOWLEDGE REQUIREMENT:

Scientific Knowledge

  • Strong knowledge of regulatory guidelines/requirements and other regional guidelines (EU and US).

  • Ability to interpret data and apply scientific knowledge to support regulatory document writing (IB, protocols, amendments, CSR, clinical summaries).

  • Ability to build clinical or regulatory arguments in the absence of direct data using logic, analogy, and therapeutic area science.

  • Understanding of medical practices regarding procedures, medications, and treatment for different disease states.

  • Ability to manage messaging for consistency with historical information and alignment with strategy.

  • Ability to provide insights, alternatives, and suggestions based on previous experience.

  • Experience writing protocols, amendments, CSR, and CTD summary documents.

Technology Skills

  • Expertise in MS Word with a strong understanding of its functionality.

  • Experience working in document management systems and managing workflows.

  • Familiarity with Word add-ins to manage fonts, styles, and references.

  • Flexibility in adapting to new tools and technology.

  • Ability to train writers/authors on the use of templates, guidelines, and tools.

RESPONSIBILITIES:

  • Prepare/review clinical study reports, protocols, investigator brochures, submission documents (Module 2 summaries), and other regulatory documents independently.

  • Apply lean authoring principles as part of document development and utilize structured content management text libraries when applicable.

  • Coordinate and initiate activities for document review, consensus meetings, quality control, and document finalization within aggressive timelines.

  • Develop and maintain project plans and work plans for team members.

  • Manage people and ensure efficient task execution.

  • Represent Medical Writing as an active member of cross-functional teams.

  • Coordinate and deliver document kick-off meetings with writers and cross-functional representatives.

  • Ensure adherence to standard content, lean authoring, and messaging across team members.

  • Ensure effective communication and dissemination of information among team members.

  • Participate in the orientation and coaching of junior team members.

  • Conduct appropriate literature searches and screening as needed.

  • Engage in Medical Writing department initiatives as appropriate.

  • Stay updated on regulatory requirements to remain current in the regulatory landscape.

  • Share lessons learned and best practices with the team.

  • Ensure compliance with company training and time reporting standards.