By using this site, you agree to the Privacy Policy and Terms of Use.
Accept
PHARMA JOBS POSTPHARMA JOBS POSTPHARMA JOBS POST
  • HOME
  • FRESHERS
  • LOCATIONS
  • ABOUT US
  • CONTACT
  • DISCLAIMER
Notification
PHARMA JOBS POSTPHARMA JOBS POST
  • HOME
  • FRESHERS
  • LOCATIONS
  • ABOUT US
  • CONTACT
  • DISCLAIMER
Have an existing account? Sign In
Follow US
PHARMA JOBS POST © 2024 All Rights Reserved.
WhatsApp Group Join Now
Telegram Group Join Now
- Advertisement -
Ad imageAd image
Ad imageAd image
PHARMA JOBS POST > Bangalore > Medical Writing Jobs at Eli Lilly – Bangalore, Karnataka | Eli Lilly and Company
BangaloreBengaluruHiringMedical Writing

Medical Writing Jobs at Eli Lilly – Bangalore, Karnataka | Eli Lilly and Company

ADMIN
Last updated: November 8, 2024 7:10 pm
ADMIN 7 months ago 26 Views
Share
SHARE

Eli Lilly and Company is hiring for a Medical Affairs – Medical Writing position at Bangalore, Karnataka, India.

Contents
Medical Affairs – Medical WritingPrimary Responsibilities:EMS (Executive Medical Summary)Project and Stakeholder managementKnowledge and Skills DevelopmentKnowledge SharingMinimum Qualification Requirements for Medical Affairs – Medical Writing positionOther Information/Additional Preferences:

Medical Affairs – Medical Writing

📍Location: Bangalore, Karnataka, India

Medical Affairs – Medical Writing

Position title/level may vary by site or geographic location

Purpose:

Scientific data and information are core assets of Lilly. Providing balanced, objective, and accurate information to regulators, the scientific community, health care professionals, payers, and patients in a consistent and timely fashion across the entire drug development lifecycle is fundamental to Lilly.

As healthcare providers are deluged with data and are making choices in an increasingly complex and stressed health system, Lilly Medical Affairs is able to provide clear, credible answers that will set Lilly apart from its competitors. Medical Affairs’ mission is to make Lilly the preferred pharmaceutical partner in the healthcare community globally by leveraging its medical expertise to drive patient-centric answers and solutions.  Medical Affairs (MA) brings deep medical expertise to healthcare providers and payers. MA focuses on answering their questions with customized clinical and real-world evidence that can make the difference on if and how they use Lilly products. Additionally, MA brings clinical insights from customers back to the company to inform new product development and lifecycle planning. MA also supports patients with educational tools to help them manage their illness and with assistance to access our medicines for those facing tough financial situations. The MA content development team will be key in   maintaining and creating content to support Medical Affairs activities such as:

Slide Updates
Internal Training Slides
Manuscript Slides
Data Slides
Newsletters/ bulletin
QR Compendium
Affiliate Regional Slides
HCP & patient education material 
Advisory board slides
Competitive landscape slides
Image sourcing, image redraws
Lexicon
MQAD (Medical Questions Analysis Document)

Primary Responsibilities:

This job description is intended to provide a general overview of the job requirements at the time it was prepared.  The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. Consult with your supervision regarding your actual job responsibilities and any related duties that may be required for the position.

EMS (Executive Medical Summary)

Content Strategy and Execution:  Document Preparation, Development and Finalization/Document Management 

Effectively collect and evaluate data, information, and input from multiple sources, functions, and regions to create a cohesive content strategy for writing projects. 

Plan (including organizing/preparing outlines), write (including first-draft authoring), edit, review, coordinate, and complete the regulatory documents supporting clinical development/product registration. 

Conduct effective document initiation meeting to ensure authoring team alignment and understanding. 

Build scientific-based rationale that support the purpose of more complex and/or strategic documents.

Ensure data are presented in a clear, complete, accurate, and concise manner. 

Ensure that key data, statements and conclusions are consistent across related documents, and that statements and conclusions are integrated, accurate, balanced and supported by appropriate data. 

Coordinate expert/scientific reviews, collate reviewer’s comments, adjust content of document as required based on internal/external input, and prepare final version. 

Ensure and coordinate quality checks for accuracy.

Exhibit flexibility in moving across development and preparation of multiple document types.

Influence or negotiate change of timelines and content with other team members.

Work with internal and external experts to develop and prepare presentations.

As needed, may build and manage relationships with vendors/ alliance partners.

Project and Stakeholder management

Lead the writing process and apply effective project management skills to ensure timely completion of high-quality regulatory documents. 

Build/communicate credible writing project timelines.

Anticipate and mitigate risks to delivery

Work with teams and stakeholders to ensure smooth and timely development of documents and escalate issues, as appropriate, to ensure document completion.  

Effectively communicate project status to stakeholders

Knowledge and Skills Development

Maintain and enhance therapeutic area knowledge including disease state and compound(s) for assigned project(s). 

Exhibit flexibility in moving across document types, therapeutic areas, and compounds, depending on project assignment. 

Maintain and enhance knowledge of regulatory guidelines and publication guidelines. 

Possess overarching view of compound, therapeutic area, and external environment (including competitors) with ability to participate effectively in clinical planning, submission strategy planning, customer regulatory responses, and/or current awareness literature updates and reviews.

Maintain and enhance the scientific communications skills to align with the audience needs and with the changes in technology and platforms. 

Knowledge Sharing

Provide coaching to others by sharing technical information, giving guidance, answering questions. 

Recognized for technical expertise in specific document development.

Network with others (including other functions and regions) to identify and share best practices.

Contribute to process improvements, suggesting opportunities where appropriate. 

Provide database and other tool (e.g., document management systems) expertise.

Minimum Qualification Requirements for Medical Affairs – Medical Writing position

Bachelor’s degree in a scientific, health, communications, technology health related field.

Demonstrated experience in technical/ regulatory scientific writing. 

Strong communication and interpersonal skills.

Successful completion of writing exercise (a writing exercise is required as part of the candidate evaluation process)

Other Information/Additional Preferences:

Graduate degree with formal research component or in life sciences. 

Demonstrated mastery of verbal and written English skills in the medical, scientific or technical writing fields.

Clinical pharmacology, therapeutic area, or other medical and scientific specific knowledge and experience specific to hiring area (e.g., neuroscience, oncology, cardiovascular, immunology or endocrine expertise). 

Experience writing regulatory, clinical trial documents and/ or publications 

Experience writing deliverables for Medical Affairs communications (slide decks, patient or HCP materials, etc)

Experience in clinical development, clinical trial process or regulatory activities. 

Demonstrated project management and time management skills. 

Demonstrated high-level end-user computer skills (e.g., word processing, tables and graphics, spreadsheets, presentation and templates).

APPLY HERE
WhatsApp Group Join Now
Telegram Group Join Now
- Advertisement -
DEFINE ACADEMY DRUG REGULATORY AFFAIRSDEFINE ACADEMY DRUG REGULATORY AFFAIRS
TAGGED: Bengaluru Pharma Vacancy, Medical Writing
Share This Article
Facebook Twitter LinkedIn Email Print
Previous Article Acme Generics Recruitment Drive: Exciting Openings in Production, Packing, and QC Departments on 09th November 2024, Saturday
Next Article QA, Engineering, Production & Packing Jobs – Akums Group | Pure & Cure Healthcare

RECENT POSTS

  • Annora Pharma Hiring Freshers,Walk-In on on June 5, 2025 for Male Apprentices in Hyderabad
  • Freshers Opportunity: Sun Pharma Apprentice Recruitment in Dewas – Apply Now
  • Join Ichor Biologics: R&D Head – Plasma-Derived Therapies & Biosimilars | Hyderabad-Based Role
  • Walk-In Interview at Aurobindo Pharma – Hiring for Production, QA, QC & Packing | 1st June 2025, Hyderabad
  • Macleods Pharma Hiring in Haridwar – Apply for Baddi & Sikkim Jobs (June 1, 2025)
  • Numandis Group Recruitment 2025 – FTE Department Hiring Freshers
  • Exciting QA & QC Job Openings at Wings Biotech
  • Career Opportunity: Production Roles at Venus Remedies
  • Walk-In Drive at OneSource (Arcolab) – Hiring for Biotech & Pharma Roles in Hyderabad | June 1, 2025
  • Walk-In Interview at Brooks Steriscience Vadodara – QC & Production Jobs (1st June 2025)
  • Vimta Careers: Walk-In Interview for Food Testing Roles – June 14
  • Walk-In Interview at Corona Remedies for ADL & QA Roles – 1st June 2025
  • R&D Careers at Apex Pharma – Formulation Specialist Wanted
JOIN WHATSAPP CHANNEL

Recent Jobs

  • Mylan Laboratories Limited

    Mylan Laboratories to Conduct Walk-In Interviews for Injectable Manufacturing Roles in Hosur

    • Hosur, Krishnagiri, Tamil Nadu
    • Mylan Laboratories Limited
  • Cadila Pharmaceuticals

    Pharma R&D Jobs: Analyst Vacancy in Analytical Research Laboratory (0–4 Years Exp) at Cadila Pharmaceuticals

    • Dholka, Ahmedabad
    • Cadila Pharmaceuticals
  • Lupin Biotech

    Lupin Biotech to Conduct Walk-in Interviews in Pune for QA, QC, and Biosimilars Roles

    • Pune, Maharashtra
    • Lupin Biotech
  • Ajanta Pharma Ltd.

    Ajanta Pharma Ltd Announces Walk-In Interviews for Multiple Roles at US FDA Approved Facility in Maharashtra

    • Chhatrapati Sambhajinagar
    • Ajanta Pharma Ltd.
  • Evertogen Lifesciences Ltd.

    Evertogen Lifesciences Ltd. Invites Fresh Talent to Join Its Team at Jadcherla Facility

    • Jadcherla
    • Evertogen Lifesciences Ltd.
  • Cadila Pharmaceuticals

    We’re Hiring: Research Associate / Sr. Research Associate – Formulation Development (Injectables)

    • Dholka, Ahmedabad
    • Cadila Pharmaceuticals
  • Sun Pharmaceutical Industries Ltd.

    Sun Pharma – Dewas is Hiring: Wruster Coating Supervisor Wanted

    • Dewas, Madhya Pradesh
    • Sun Pharmaceutical Industries Ltd.
  • Biodeal Pharmaceuticals Ltd

    Biodeal Pharmaceuticals Ltd. is Hiring! Explore Career Opportunities in QC, R&D, and Production

    • Nalagarh
    • Biodeal Pharmaceuticals Ltd
  • Scientific Writing Jobs at Indegene – Open to Freshers and Experienced Candidates (0–2 Years)

    • Anywhere
  • IQVIA

    IQVIA is Hiring Freshers! Kickstart Your Consulting Career in Healthcare

    • Bengaluru, India
    • IQVIA
  • Biological E. Limited

    Biological E. Limited is hiring for Regulatory Affairs Department

    • Genome Valley, Shameerpet, Hyderabad
    • Biological E. Limited
  • Genedrift

    Genedrift is Hiring: Regulatory Affairs Roles Open (Entry & Senior Level)

    • Uttarakhand
    • Genedrift

Tags

Ahmedabad (65) ahmedabad pharma jobs (189) ahmedabad pharma vacancy (165) ahmedabad pharma walk in interview (89) Baddi Pharma Vacancy (59) Bangalore pharma company jobs (41) Bangalore pharma jobs (31) FRESHERS (181) freshers jobs in pharma industry (50) freshers pharmacy jobs (46) goa pharma company job (27) Hiring (119) Hiring jobs (461) Hyderabad (57) hyderabad pharma company jobs (184) hyderabad pharma jobs (94) hyderabad pharma jobs freshers (42) hyderabad pharma vacancies (111) hyd pharma jobs (31) indore pharma company vacancy (27) job alert (382) job Opportunity (246) Job search (460) job Vaccancy (450) Mumbai Pharma company jobs (34) Pharmacovigilance Jobs vacancy (38) Pharma jobs (104) Pharma jobs at Baddi (36) pharma jobs in hyderabad (84) Pharma QA Jobs (35) pharma qa vacancy (28) pharma vacancy in ahmedabad (30) pharma walk in interview (44) Production (58) Production Department (73) QA (53) QC (77) QC Department (45) Quality Control (QC) (32) Regulatory Affairs (55) Regulatory Affairs Jobs Vacancy (63) Vadodara (33) Vadodara Pharma Job Vacancy (53) Walk In Drive (125) Walk In Interview (180)
PHARMA JOBS POSTPHARMA JOBS POST
Follow US
PHARMA JOBS POST © 2024 All Rights Reserved.
JOIN OUR WHATSAPP GROUP
JOIN OUR TELEGRAM GROUP
Welcome Back!

Sign in to your account

Lost your password?