7 Scientific Writing jobs in India

Scientific Writing Intern

Bengaluru, Karnataka BioTecNika

Posted 5 days ago

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Job Description

Key Responsibilities:

● Content Research & Curation: Identify, verify, and prepare relevant biotech/life science opportunities, updates, and resources for our audience.

● Article Writing: Create engaging career guidance articles tailored to students and professionals.

● News & Research Summaries: Curate and simplify the latest developments in biotechnology, life sciences, and allied fields.

● Creative & Media Support: Assist in designing presentations, brochures, posters, infographics, and social media creatives.

● Engagement & Outreach: Ensure all content is clear, accurate, and engaging to connect effectively with readers.


Digital Skills and Tools Utilization:

● Social Media Engagement: Utilize LinkedIn, Instagram, Facebook, and YouTube to increase visibility and engage relevant audiences.

● Email Marketing and Web Presence: Implement email marketing strategies and maintain an active website.

● Data Mining and Analysis: Employ analytical tools to gather information on target audiences, including email addresses and LinkedIn profiles, and trade show participation.


Educational Requirements:

● Bachelor’s or Master’s degree in life sciences, biotechnology, Chemistry, pharma or a related field.

● Proven passion and ability for writing and must be a voracious reader.

● Strong research skills and attention to detail.

● Knowledge of scientific writing and digital content creation.

● Familiarity with social media platforms and digital marketing concepts.

● Ability to work independently and in a team.

● Enthusiasm for learning about industry trends.


Benefits:

● Work with an international life sciences company and leading life sciences and

biotechnology news portal Biotecnika.

● Gain experience in scientific writing, journalism, and digital marketing.

● Exposure to the latest trends and developments in life sciences and

biotechnology.

● Networking opportunities with professionals and researchers.

● Certificate of completion at the end of the internship.


Duration: The internship will be for a period of six months, with the possibility of an

extension based on performance.

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Experienced Scientific Writing Author

Fengkai Group Co., Limited

Posted 5 days ago

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Job Description

Responsibilities


  • Taking ownership and responsibility for development (write, review, proofread, and data-check) of high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client and audience needs with excellent attention to detail.
  • Actively involved in reviewing materials developed by scientific writers to ensure strategic alignment and scientific accuracy as needed and providing clear constructive feedback, support, and supervision to writers. Mentor and train scientific writers by sharing best practices and client preferences, thereby contributing to skill development within the team.
  • Having excellent knowledge of product/account to enable meaningful interactions with clients and authors, including consultancy where necessary. Liaising and building and maintaining strong and long-standing professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs. This includes educating and advising clients on how to best implement their strategic and tactical plans and proactively provide recommendations to clients on how to improve scientific content and propose new document types/ways to disseminate client date more effectively.
  • Effectively and proactively communicate with team members, authors/faculty, clients and vendors.
  • Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives.
  • Attending client and other external meetings and supporting senior team members as needed
  • Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans. Also, Supporting with the development of visual content and materials using effective data visualization techniques and approaches. Contributing to innovative “out of the box” solutions for medical writing projects.
  • You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and FengKai internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
  • Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines.
  • Supporting with pitches, both during the preparation phase and the actual pitch.


Qualifications and Prerequisites

  • Minimum of 3 years of experience in relevant fields of scientific writing.
  • Possess a Ph.D. in Pharmacology, M.D., Ph.D. in Life Sciences, Pharm.D., or Ed.D.
  • Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills.
  • Ability to adapt writing style to different materials and target audiences.
  • Basic knowledge of biostatistics.
  • Literature reviewing and evaluation capabilities.
  • Very good working knowledge of MS Office.
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Experienced Scientific Writing Author

Fengkai Group Co., Limited

Posted 5 days ago

Job Viewed

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Job Description

Responsibilities


  • Taking ownership and responsibility for development (write, review, proofread, and data-check) of high-quality, client-ready scientific, medical, and educational materials like slides, abstracts, posters, manuscripts, MSL/training slide decks, infographics, congress and meetings materials, literature searches and reviews, standard response letters/medical information letters, and HCP engagement content according to client and audience needs with excellent attention to detail.
  • Actively involved in reviewing materials developed by scientific writers to ensure strategic alignment and scientific accuracy as needed and providing clear constructive feedback, support, and supervision to writers. Mentor and train scientific writers by sharing best practices and client preferences, thereby contributing to skill development within the team.
  • Having excellent knowledge of product/account to enable meaningful interactions with clients and authors, including consultancy where necessary. Liaising and building and maintaining strong and long-standing professional relationships with international pharmaceutical clients, healthcare professionals, internal and external stakeholders including authors, reviewers and key opinion leaders across therapeutic areas -- learning to anticipate their needs. This includes educating and advising clients on how to best implement their strategic and tactical plans and proactively provide recommendations to clients on how to improve scientific content and propose new document types/ways to disseminate client date more effectively.
  • Effectively and proactively communicate with team members, authors/faculty, clients and vendors.
  • Attend workshops/seminars/trainings to hone your skills and contribute to organizational objectives.
  • Attending client and other external meetings and supporting senior team members as needed
  • Apply your scientific and creative knowledge and work closely with client directors in developing ideas and executing effective medical communications initiatives in the digital space, including publication extenders, creation of infographics, interactive assets, website content, patient narratives, and medical information engagement plans. Also, Supporting with the development of visual content and materials using effective data visualization techniques and approaches. Contributing to innovative “out of the box” solutions for medical writing projects.
  • You will be responsible for ensuring all materials follow/comply with client requirements/SOPs, style guides, client templates, client preferences (as applicable), and FengKai internal SOPs. Any updates to either of these items should be made consistently and documents should remain up to date.
  • Perform as a document specialist, provide intellectual input across document types, and contribute to making cutting-edge research accessible to specific audiences as appropriate, by maintaining current awareness of developments across therapeutic areas or disciplines.
  • Supporting with pitches, both during the preparation phase and the actual pitch.


Qualifications and Prerequisites

  • Minimum of 3 years of experience in relevant fields of scientific writing.
  • Possess a Ph.D. in Pharmacology, M.D., Ph.D. in Life Sciences, Pharm.D., or Ed.D.
  • Clear, concise, scientific style of writing, with a high level of attention to detail and excellent language skills.
  • Ability to adapt writing style to different materials and target audiences.
  • Basic knowledge of biostatistics.
  • Literature reviewing and evaluation capabilities.
  • Very good working knowledge of MS Office.
This advertiser has chosen not to accept applicants from your region.

Technical Writing Services Analyst I

Noida, Uttar Pradesh Conduent

Posted 2 days ago

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Job Description

Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments - creating exceptional outcomes for our clients and the millions of people who count on them. You have an opportunity to personally thrive, make a difference and be part of a culture where individuality is noticed and valued every day.
**Communication Skills**
**Excellent English Communication:** The candidate must possess very good English communication skills to effectively interact with clients, facilitators, and attendees before and during live sessions.
**Session Management**
**Deployment Responsibility:** The individual should demonstrate strong organizational skills to ensure the successful deployment of each session moderated.
**Live Session Hosting:** Experience in hosting live sessions on platforms such as MS Teams (or other related virtual platforms like Zoom, or WebEx) is crucial. This includes managing dry runs and rehearsals, and ensuring all technical aspects are functioning correctly.
**Client Interaction**
**High-Level Client Engagement:** The candidate must be comfortable working with high-level clients, scheduling and setting up sessions, sending invites, and managing announcements.
**Technical Proficiency**
**Platform Familiarity:** Familiarity with MS Teams Meetings & Townhall (or similar platforms) is advantageous. The moderator should be able to navigate these tools confidently to facilitate sessions.
**Technology Support:** Providing technical support to both facilitators and learners is essential. This includes addressing technology-related concerns and questions related to the MS Teams platform.
**Administrative Skills**
**Session Preparation:** The candidate should excel in gathering necessary materials for sessions (slides, videos, agendas) and managing administrative tasks such as uploading course materials and launching polling questions.
**Post-Session Reporting:** Ability to provide detailed post-session reports, marking attendance, and send materials to clients is required.
**Interactive Management**
**Breakout Room Management** : Experience in managing breakout room activities, both manually and automatically, is important for facilitating small group discussions.
**Poll Management:** Skills in creating and managing polls during sessions to engage attendees effectively.
**Problem-Solving Abilities**
**Troubleshooting Skills:** The moderator should have strong problem-solving and multi-tasking skills to address any technical issues that arise during live sessions swiftly via chat, q&a, and/or email.
Conduent is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, creed, religion, ancestry, national origin, age, gender identity, gender expression, sex/gender, marital status, sexual orientation, physical or mental disability, medical condition, use of a guide dog or service animal, military/veteran status, citizenship status, basis of genetic information, or any other group protected by law.
For US applicants: People with disabilities who need a reasonable accommodation to apply for or compete for employment with Conduent may request such accommodation(s) by submitting their request through this form that must be downloaded: click here to access or download the form ( . Complete the form and then email it as an attachment to . You may also click here to access Conduent's ADAAA Accommodation Policy ( .
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Associate Analyst - PSA Records Maintenance / Technical Writing [T500-20760]

Hyderabad, Andhra Pradesh ANSR

Posted 5 days ago

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Job Description

ANSR is hiring for one of its clients.

About American Airlines:

To Care for People on Life's Journey®. We have a relentless drive for innovation and excellence. Whether you're engaging with customers at the airport or advancing our IT infrastructure, every team member plays a vital role in shaping the future of travel. At American’s Tech Hubs, we tackle complex challenges and pioneer cutting-edge technologies that redefine the travel experience. Our vast network and diverse customer base offer unique opportunities for engineers to solve real-world problems on a grand scale. Join us and immerse yourself in a dynamic, tech-driven environment where your creativity and unique strengths are celebrated. Experience the excitement of being at the forefront of technological innovation, where every day brings new opportunities to make a meaningful impact.


About Tech Hub in India:

American’s Tech Hub in Hyderabad, India, is our newest location and home to team members who drive technical innovation and engineer unrivalled digital products to best serve American’s customers and team members. With U.S. tech hubs in Dallas-Fort Worth, Texas and Phoenix, Arizona, our new location in Hyderabad, India, positions American to deliver industry-leading technology solutions that create a world-class customer experience.


ANALYST, RECORDS MAINTENANCE

INTRO:

Are you ready to explore a world of possibilities, both at work and during your time off? Join our PSA family, grow your expertise, and become the best version of you. As you embark on a new journey, you’ll tackle challenges with flexibility and grace, learning new skills and advancing your career while having the time of your life. Feel free to enrich both your personal and work life and hop onboard!


WHY YOU’LL LOVE THIS JOB:

The Analyst, Records Maintenance is part of PSA’s Tech Ops Division in the PSA Tech Services Center. This role will utilize technical writing and records management skills to ensure safe, reliable operations and compliance with regulatory requirements.


WHAT YOU’LL DO:

This list is intended to reflect the current job but there may be additional essential functions (and certainly non-essential job functions) that are not referenced. Management will modify the job or require other tasks be performed whenever it is deemed appropriate to do so, observing, of course, any legal obligations including any collective bargaining obligations.

  • Provide technical writing, revision, and electronic management services for all PSA manuals, forms, and work instructions
  • Author and revise Job Instruction Cards as required
  • Distribute internal communications, OEM manuals, and PSA controlled manuals to the frontline team per GMM requirements
  • Collect and resolve RFTSs for publication changes submitted by the frontline
  • Ensure all Tech Ops records are audited, stored, and indexed properly to ensure GMM compliance
  • Perform ad-hoc records reviews as assigned
  • Serve as a transaction redundancy in case the MRO system is unavailable within PSA's GMM guidelines
  • Other duties as assigned by Tech Services leadership


ALL YOU’LL NEED FOR SUCCESS

Minimum Qualifications – Education & Prior Job Experience:

  • Bachelor's degree in an operations management, industrial engineering, mechanical engineering, or related field
  • 3 years of experience in Tech Ops or a related field
  • FAA 121 Airline Operator and associate FARs or equivalent experience


Preferred Qualifications – Education & Prior Job Experience:

  • Experience in technical writing and editing
  • Familiarity with aviation industry regulations and compliance
  • Experience with electronic document management systems


Skills, Licenses, and Certifications:

  • Strong technical writing and editing skills
  • Excellent communication and collaboration skills
  • Familiarity with regulatory requirements and compliance
  • Proficiency in Microsoft Office and electronic document management systems
  • Ability to work in a fast-paced environment and prioritize multiple tasks


LANGUAGE / COMMUNICATION SKILLS:

  • Ability to effectively communicate both verbally and written with all levels within the organization
  • Physical ability necessary to safely and successfully perform the essential functions of the position, with or without any legally required reasonable accommodations that do not pose an undue hardship.

Note: If the Company has reason to question an employee’s physical ability to safely and/or successfully perform the position’s essential job functions, the HR team generally will engage in an interactive process to determine whether a reasonable accommodation is appropriate. HR (working with the operation) ordinarily first speaks with the team member directly and they mutually identify the physical demands of the job that are or may be impacted by the employee’s obvious or known condition. Then, if necessary, HR would request medical documentation from the team member’s treating physician or others to confirm the employee’s ability to perform those essential job functions safely and successfully.


COMPETENCIES:

  • Caring
  • Collaboration
  • Development
  • Future
  • Results
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Manager Medical Writing

Bengaluru, Karnataka Omnicom

Posted 5 days ago

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Job Description

We have an exciting role of Medical Writer - Manager to drive and translate creative and contemporary ideas to solid design and impact. You will have a key role in design and deployment of creative campaigns with our global clients, including many Fortune 50 companies.


About US

We are an integral part of Annalect Global and Omnicom Group, one of the largest media and advertising agency holding companies in the world. Omnicom’s branded networks and numerous specialty firms provide advertising, strategic media planning and buying, digital and interactive marketing, direct and promotional marketing, public relations, and other specialty communications services. Our agency brands are consistently recognized as being among the world’s creative best.

Annalect India plays a key role for our group companies by providing stellar products and services in areas of Creative Services, Technology, Marketing Science (data & analytics), Market Research, Business Support Services, Media Services, Consulting & Advisory Services. We are growing rapidly and looking for talented professionals like you to be part of this journey. Let us build this, together!



This is an exciting role and would entail you to

  • Write clear, engaging, and medically accurate content for a range of audiences — including press materials, consumer
  • campaigns, digital assets, and educational tools.
  • Translate complex clinical and scientific information into language that resonates with non-specialist audiences, including patients, caregivers, and media outlets.
  • Develop messaging that aligns with brand strategy, while simplifying technical data for broader understanding without compromising accuracy.
  • Partner with internal teams (account, strategy, and creative) to ideate and execute content that is impactful, on-brand, and compliant.
  • Revise and refine copy based on internal and client feedback and MLR reviewer input.

You will be working closely with

Our global creative agency teams. You will also be closely collaborating with our team of talented and designers to deliver high-quality services.

This may be the right role for you if you have

  • 11+ years of experience in healthcare communications agencies (AMA experience is preferred)
  • Bachelor's degree or equivalent experience with a focus on pharma/science/medicine
  • Portfolio containing work samples that demonstrate medical writing for a variety of communication forms (e.g., sales aids, direct mail, websites, social media) for a variety of audiences (e.g., healthcare professionals, patients, consumers)
  • AMA Style Guide knowledge (certification not mandatory)
  • Experience with referencing and annotating, and client MLR submissions requirements
  • An ability to understand and process healthcare information
  • Able to multi-task in a faced paced environment as a member of a highly collaborative team
  • The desire to work with a diverse group of teams, projects, and clients
  • Strong conceptual ability, standout creative thinking, and top-notch writing skills
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Pharma SME (Medical Writing)

Pune, Maharashtra UsefulBI Corporation

Posted 5 days ago

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Job Description

We are hiring Pharma SME – Medical Writing

Experience: 5–8 years

Industry: Pharmaceutical

Shift Timing: 2 pm to 11 pm

Locations: Pune/Bangalore/Lucknow


Key Responsibilities:

  • Develop, review, and finalize scientific and regulatory documents including clinical study reports (CSRs), protocols, investigator brochures (IBs), and safety narratives.
  • Ensure all documents adhere to ICH-GCP, regulatory, and company standards.
  • Translate complex clinical data into clear, concise, and scientifically accurate documents.
  • Collaborate with cross-functional teams including clinical research, medical affairs, and regulatory affairs for content accuracy.
  • Provide guidance and mentorship to junior medical writers and ensure quality control of deliverables.


Skills & Competencies:

  • Proficiency in scientific writing and regulatory documentation.
  • Sound understanding of clinical trial phases, statistical concepts, and medical terminology.
  • Strong editorial, grammar, and formatting skills with attention to detail.
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