128 Scientific Writing jobs in India

Scientific Writing Lead

Bengaluru, Karnataka Indegene

Posted 4 days ago

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Job Description

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast-track career where you can grow along with Indegene’s high-speed growth. We are purpose-driven. We enable healthcare organizations to be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work.


Scientific Writing Lead

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


Key Responsibilities:

  • Serve as a subject matter expert for medical communications, including reactive and proactive decks, medical information letters, infographics, quick response guides, verbal response documents, FAQs, and product monographs.
  • Demonstrate expertise and knowledge of assigned therapeutic areas and a good understanding of pertinent disease states and clinical trials.
  • Conduct medical reviews and data fact-checks on MedComm deliverables.
  • Deliver high-quality literature searches, including identifying key literature to support the creation of medical content and obtaining copyright permissions prior to internal or external use.
  • Recognize client business needs and align team capabilities accordingly.
  • Lead and upskill a team of scientific writers as part of the training process.
  • Prepare and update specific training documents as needed.
  • Participate in routine client meetings and lead these meetings when necessary. Plan and scope projects from the kick-off call to submission.
  • Deliver exceptional documents and maintain client satisfaction metrics.
  • Collaborate cross-functionally with quality assurance, creative, copy-editing, business excellence, and project management teams.
  • Utilize reference manager tools and CRM platforms.

Requirements:

  • MBBS, MD, BDS, MDS, Doctorate in research, or pharmacy qualification (Postgraduate in Pharmacy, PharmD., Ph.D.).
  • 4-12 years of experience in medical communication, with additional experience in scientific writing, content writing, medical review, or publication experience in the life sciences domain.

Skills:

  • Strong medical writing and literature surveillance skills.
  • Excellent oral and written communication skills in English.
  • Preferably have knowledge about the Veeva platform.


Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, the candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

This advertiser has chosen not to accept applicants from your region.

Scientific Writing Lead

Bengaluru, Karnataka Indegene

Posted today

Job Viewed

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Job Description

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast-track career where you can grow along with Indegene’s high-speed growth. We are purpose-driven. We enable healthcare organizations to be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work.

Scientific Writing Lead

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

Key Responsibilities:

  • Serve as a subject matter expert for medical communications, including reactive and proactive decks, medical information letters, infographics, quick response guides, verbal response documents, FAQs, and product monographs.
  • Demonstrate expertise and knowledge of assigned therapeutic areas and a good understanding of pertinent disease states and clinical trials.
  • Conduct medical reviews and data fact-checks on MedComm deliverables.
  • Deliver high-quality literature searches, including identifying key literature to support the creation of medical content and obtaining copyright permissions prior to internal or external use.
  • Recognize client business needs and align team capabilities accordingly.
  • Lead and upskill a team of scientific writers as part of the training process.
  • Prepare and update specific training documents as needed.
  • Participate in routine client meetings and lead these meetings when necessary. Plan and scope projects from the kick-off call to submission.
  • Deliver exceptional documents and maintain client satisfaction metrics.
  • Collaborate cross-functionally with quality assurance, creative, copy-editing, business excellence, and project management teams.
  • Utilize reference manager tools and CRM platforms.

Requirements:

  • MBBS, MD, BDS, MDS, Doctorate in research, or pharmacy qualification (Postgraduate in Pharmacy, PharmD., Ph.D.).
  • 4-12 years of experience in medical communication, with additional experience in scientific writing, content writing, medical review, or publication experience in the life sciences domain.

Skills:

  • Strong medical writing and literature surveillance skills.
  • Excellent oral and written communication skills in English.
  • Preferably have knowledge about the Veeva platform.

Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, the candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

This advertiser has chosen not to accept applicants from your region.

Scientific writing lead

Bengaluru, Karnataka Indegene

Posted today

Job Viewed

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Job Description

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast-track career where you can grow along with Indegene’s high-speed growth. We are purpose-driven. We enable healthcare organizations to be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work.Scientific Writing LeadWe are a technology-led healthcare solutions provider driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy.Key Responsibilities:Serve as a subject matter expert for medical communications, including reactive and proactive decks, medical information letters, infographics, quick response guides, verbal response documents, FAQs, and product monographs.Demonstrate expertise and knowledge of assigned therapeutic areas and a good understanding of pertinent disease states and clinical trials.Conduct medical reviews and data fact-checks on Med Comm deliverables.Deliver high-quality literature searches, including identifying key literature to support the creation of medical content and obtaining copyright permissions prior to internal or external use.Recognize client business needs and align team capabilities accordingly.Lead and upskill a team of scientific writers as part of the training process.Prepare and update specific training documents as needed.Participate in routine client meetings and lead these meetings when necessary. Plan and scope projects from the kick-off call to submission.Deliver exceptional documents and maintain client satisfaction metrics.Collaborate cross-functionally with quality assurance, creative, copy-editing, business excellence, and project management teams.Utilize reference manager tools and CRM platforms.Requirements:MBBS, MD, BDS, MDS, Doctorate in research, or pharmacy qualification (Postgraduate in Pharmacy, Pharm D., Ph. D.).4-12 years of experience in medical communication, with additional experience in scientific writing, content writing, medical review, or publication experience in the life sciences domain.Skills:Strong medical writing and literature surveillance skills.Excellent oral and written communication skills in English.Preferably have knowledge about the Veeva platform.Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, the candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.

This advertiser has chosen not to accept applicants from your region.

Scientific Writing Lead

Bengaluru, Karnataka Indegene

Posted 4 days ago

Job Viewed

Tap Again To Close

Job Description

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast-track career where you can grow along with Indegene’s high-speed growth. We are purpose-driven. We enable healthcare organizations to be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work.

Scientific Writing Lead
We are a technology-led healthcare solutions provider driven by our purpose to enable healthcare organizations to be future-ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious, and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy.

Key Responsibilities:
Serve as a subject matter expert for medical communications, including reactive and proactive decks, medical information letters, infographics, quick response guides, verbal response documents, FAQs, and product monographs.
Demonstrate expertise and knowledge of assigned therapeutic areas and a good understanding of pertinent disease states and clinical trials.
Conduct medical reviews and data fact-checks on MedComm deliverables.
Deliver high-quality literature searches, including identifying key literature to support the creation of medical content and obtaining copyright permissions prior to internal or external use.
Recognize client business needs and align team capabilities accordingly.
Lead and upskill a team of scientific writers as part of the training process.
Prepare and update specific training documents as needed.
Participate in routine client meetings and lead these meetings when necessary. Plan and scope projects from the kick-off call to submission.
Deliver exceptional documents and maintain client satisfaction metrics.
Collaborate cross-functionally with quality assurance, creative, copy-editing, business excellence, and project management teams.
Utilize reference manager tools and CRM platforms.
Requirements:
MBBS, MD, BDS, MDS, Doctorate in research, or pharmacy qualification (Postgraduate in Pharmacy, PharmD., Ph.D.).
4-12 years of experience in medical communication, with additional experience in scientific writing, content writing, medical review, or publication experience in the life sciences domain.
Skills:
Strong medical writing and literature surveillance skills.
Excellent oral and written communication skills in English.
Preferably have knowledge about the Veeva platform.

Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, the candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.
This advertiser has chosen not to accept applicants from your region.

Associate - Scientific Writing

Bengaluru, Karnataka Indegene

Posted today

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Job Description

Looking to jump-start your career?

We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast track career where you can grow along with Indegene’s high-speed growth.

We are purpose-driven.
** **We enable healthcare organizations be future ready and our customer obsession is our driving force
**.** We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work.

**Associate - Scientific Writing**

**You will be responsible for**:
"- Create/review Drug Files (Generic Formulation, Manufacturing Entity, Healthcare Product, Package), Drug Interactions, Pharmacokinetics, Physicochemical Properties, Reproductive Effects (Pregnancy and Lactation), Product Citations and Company Authoring Units in Content Management System from labelling documents for all international locales and USA as needed.
- Create/update/maintain content in Medication Advisory Screening tool for Therapeutic Classes, Disease Concepts, Warnings, General Precautions and Allergens from labelling documents for all international locales and USA as needed.
- Update/maintain data created for all international locales and USA as needed."

**Your impact**:
**About you**:(Desired profile)

**Must have**:Understand the principles and concepts associated with case-handling process and overall Drug Research Process. - Cognitive abilities including verbal reasoning, attention to detail, and critical and analytical thinking. - Good knowledge on therapy area/medical terminology. - Good comprehension skills. - Good communication (verbal and written), with fluency in English and interpersonal skills.

**EQUAL OPPORTUNITY**

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.
This advertiser has chosen not to accept applicants from your region.

Associate - Scientific Writing

Bengaluru, Karnataka Indegene

Posted today

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Job Description

What if we told you that you can move to an exciting role in an entrepreneurial organization without the usual risks associated with it?

We understand that you are looking for growth in your career at this point and we would love for you to join us in our journey and grow with us. At Indegene, our roles come with the excitement you require at this stage of your career with the reliability you seek. We believe in creating leaders of tomorrow and mentor our leads to help them grow and nurture them as people managers and account managers.

We are a rapidly growing global organization and are scouting for the best talent for this phase of growth. With us, you are at the intersection of two of the most exciting industries of healthcare and technology. We offer global opportunities with fast-track careers while you work with a team that is fueled by purpose. The combination of this will lead to a truly differentiated experience for you.

**You will be responsible for**:

- Review of promotional and medical communication materials (for various client products) and ensure the content in these materials is medically accurate, scientifically rigorous, truthful and balanced, relevant to product and therapy area, compliant to various pharma regulations and guidelines and is supported by authentic and up to date references.
- Develop and update content for various medical materials, perform literature search to identify appropriate references to support creation/update of scientific content, track and audit assets for various purposes.
- Develop and review content for various deliverables meeting quality requirements as per client satisfaction metrics, within assigned timelines and with guidance from the manager. The tasks will be carried out as per assigned processes, guidelines, and SOPs with help of tools and platforms specified by the client and the manager.
- Responsible to follow the best practices in the department regarding - processes, communication (internal & external), project management, documentation, and technical requirements like - language, grammar, stylization, content search, summarizing, data conflicts and referencing.
- Participate in assigned training programs and work on assignments as per requirement.
- Participate in client calls as per project requirements.
- Compliance to quality, confidentiality and security; Adhere and follow quality systems, processes and policies; Comply to training and specifications

**Your impact**:
**About you**:
Prior work experience in medical information domain (2-5 years) is required for this position.

**Must have**:

- Education— MD/MDS/PhD with Post Doc (or experience)/MBBS with experience
- Minimum 2 to 4 years of experience in pharmaceutical companies
- Understanding of any specialty area of medicine (preferred) or an overall understanding of the medical field
- Strong flair and passion for writing
- Strong written and verbal communication/presentation skills
- Passion for networking
- Being up to date with the latest technical/scientific developments and relating them to various projects
- Client-oriented attitude with focus on creating strong long-term relationships with clients and encouraging others to work toward this goal
- Ability to assure timely completion of assignments
- Skilled in problem identification and problem solving

**EQUAL OPPORTUNITY**

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.
This advertiser has chosen not to accept applicants from your region.

Research Analyst – Scientific Writing

Andhra Pradesh, Andhra Pradesh Katalyst HealthCares & Life Sciences

Posted today

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Job Description


Job Description:
  • We are seeking a Research Analyst (Scientific Writing) to join our team and support the development of high-quality scientific documents, publications, and research-based content.
  • The ideal candidate will have a strong background in life sciences, biotechnology, or pharmaceuticals, combined with excellent skills in scientific writing, data interpretation, and literature analysis.
  • This role involves transforming complex scientific data into clear, accurate, and impactful content for research reports, white papers, regulatory documents, manuscripts, and client deliverables.
  • Responsibilities:
  • Conduct in-depth literature reviews and gather relevant scientific data from peer-reviewed journals, databases, and clinical reports.
  • Analyze and synthesize scientific information to prepare well-structured documents, including research summaries, manuscripts, white papers, and regulatory content.
  • Collaborate with scientists, subject matter experts, and cross-functional teams to ensure accuracy, clarity, and consistency of written materials.
  • Prepare data-driven reports and presentations for internal and external stakeholders.
  • Ensure compliance with scientific, ethical, and regulatory writing standards (, ICH, GCP, CONSORT, or similar).
  • Stay updated with current developments in life sciences, healthcare, and biotechnology sectors.
  • Requirements:
  • Master's or PhD in Life Sciences, Biotechnology, Pharmacy, Medicine, or related field.
  • Proven experience in scientific/medical writing or research analysis.
  • Strong ability to critically analyze data and translate complex concepts into clear, concise narratives.
  • Proficiency with scientific databases (PubMed, Embase, Scopus, etc.) and reference management tools (EndNote, Mendeley, Zotero).
  • Excellent written and verbal communication skills with attention to detail.
  • Familiarity with statistical analysis and clinical trial design is a plus.
  • Ability to work independently, manage deadlines, and handle multiple projects.
  • What We Offer:
  • Opportunity to work on impactful projects in the life sciences and healthcare sector.
  • A collaborative environment with scientists, researchers, and industry experts.
  • Professional development and training in scientific writing and research methodology.
  • Competitive compensation package with growth opportunities.

  • This advertiser has chosen not to accept applicants from your region.
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    Team Lead - Scientific Writing

    Confidential

    Posted today

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    Job Description

    Job title: Team Lead - Scientific Writing

    Hiring Manager: Head/Group Lead - Scientific Writing

    Location: Hyderabad

    % of travel expected: As per business need

    Job type: Permanent and Full time

    About the job

    Our Team:

    Sanofi Global Hub (SGH) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and RD, Data Digital functions. SGH strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally.

    Main responsibilities:

    The overall purpose and main responsibilities are listed below:

    To create synergies and provide functional and operational direction to assigned therapeutic area(s) (TA(s)) and processes; act as strategic thought partner to the TA Scientific communication lead; lead team of writers for assigned TA, and coach and develop expert and senior writers; provide input to publication and communication plans and ensure delivery as per plan; develop and maintain expertise in TA and on key trends/developments in the industry; and collaborate effectively with stakeholders.

    People:

    1. Lead team of writers (junior to expert) or similar roles (in content creation)
    2. Coach and develop expert and senior writers or similar roles (on content/methods/processes)
    3. Maintain effective relationship with the end stakeholders (medical scientific community) within the allocated TA/GBU and product - with an end objective to develop education and communication content as per requirement
    4. Ensure new technologies are leveraged

    Performance:

    1. Act as strategic thought partner to assigned TA(s) within an assigned GBU
    2. Develop and maintain expertise in assigned TA and on key trends/developments in the industry
    3. Provide inputs for publication and communication plan/publication and medical education materials/other strategic deliverables, and ensure delivery as per plan (agreed timelines and quality)
    4. Lead and support development of tools, technology, and processes in order to constantly improve quality and productivity

    Process:

    1. Support delivery of projects in terms of resourcing, quality, timeliness, efficiency, and high technical standards for deliveries made by the medical writing group, including scientific documents and clinical/medical reports
    2. Contribute to overall quality enhancement by ensuring high scientific standards for the output produced by the scientific writing group
    3. Secure adherence to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory standards
    4. Ensure all publication and medical education materials are delivered as per agreed timelines and quality
    5. Ensure creating and developing tools, technology, and process to constantly improve quality and productivity
    6. Leverage advanced training delivery tools and techniques thereby enhancing the effectiveness of training delivery

    Stakeholder:

    1. Work closely with scientific communication teams in regions/areas to identify publication need and assist in developing assigned deliverables
    2. Maintain effective relationship with the end stakeholders (medical scientific community) with an end objective to develop education and communication content as per requirement
    About you

    Experience:

    • 10 years of experience in content creation for the pharmaceutical/healthcare industry, or academia
    6 years of experience in leadership role
    • Ability to influence and negotiate

    Soft skills:

    • Stakeholder management
    • Communication skills
    • People management
    • Ability to work independently and within a team environment

    Technical skills:

    As applicable (including but not limited to):

    • Therapeutic area/domain knowledge exposure
    • Proficient in multiple TAs/domains under one GBU
    • Scientific communications/writing
    • Medical communications/writing
    • Publication planning
    • Project management

    Education:

    Advanced degree in life sciences/pharmacy/similar discipline or medical degree

    Languages:

    Excellent knowledge of English language (spoken and written)

    Pursue progress, discover extraordinary

    Better is out there. Better medications, better outcomes, better science. But progress doesn't happen without people - people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let's be those people.

    At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

    Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!


    Skills Required
    Stakeholder Management, Scientific Writing
    This advertiser has chosen not to accept applicants from your region.

    Research Analyst – Scientific Writing

    Andhra Pradesh, Andhra Pradesh cGxPServe

    Posted today

    Job Viewed

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    Job Description

    Job Description:

    • We are seeking a Research Analyst (Scientific Writing) to join our team and support the development of high-quality scientific documents, publications, and research-based content.
    • The ideal candidate will have a strong background in life sciences, biotechnology, or pharmaceuticals, combined with excellent skills in scientific writing, data interpretation, and literature analysis.
    • This role involves transforming complex scientific data into clear, accurate, and impactful content for research reports, white papers, regulatory documents, manuscripts, and client deliverables.

    Responsibilities:

    • Conduct in-depth literature reviews and gather relevant scientific data from peer-reviewed journals, databases, and clinical reports.
    • Analyze and synthesize scientific information to prepare well-structured documents, including research summaries, manuscripts, white papers, and regulatory content.
    • Collaborate with scientists, subject matter experts, and cross-functional teams to ensure accuracy, clarity, and consistency of written materials.
    • Prepare data-driven reports and presentations for internal and external stakeholders.
    • Ensure compliance with scientific, ethical, and regulatory writing standards (e.g., ICH, GCP, CONSORT, or similar).
    • Stay updated with current developments in life sciences, healthcare, and biotechnology sectors.

    Requirements:

    • Master s or PhD in Life Sciences, Biotechnology, Pharmacy, Medicine, or related field.
    • Proven experience in scientific/medical writing or research analysis.
    • Strong ability to critically analyze data and translate complex concepts into clear, concise narratives.
    • Proficiency with scientific databases (PubMed, Embase, Scopus, etc.) and reference management tools (EndNote, Mendeley, Zotero).
    • Excellent written and verbal communication skills with attention to detail.
    • Familiarity with statistical analysis and clinical trial design is a plus.
    • Ability to work independently, manage deadlines, and handle multiple projects.

    What We Offer:

    • Opportunity to work on impactful projects in the life sciences and healthcare sector.
    • A collaborative environment with scientists, researchers, and industry experts.
    • Professional development and training in scientific writing and research methodology.
    • Competitive compensation package with growth opportunities.
    This advertiser has chosen not to accept applicants from your region.

    Research Analyst – Scientific Writing

    Guntur, Andhra Pradesh Katalyst HealthCares & Life Sciences

    Posted today

    Job Viewed

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    Job Description


    Job Description:
  • We are seeking a Research Analyst (Scientific Writing) to join our team and support the development of high-quality scientific documents, publications, and research-based content.
  • The ideal candidate will have a strong background in life sciences, biotechnology, or pharmaceuticals, combined with excellent skills in scientific writing, data interpretation, and literature analysis.
  • This role involves transforming complex scientific data into clear, accurate, and impactful content for research reports, white papers, regulatory documents, manuscripts, and client deliverables.
  • Responsibilities:
  • Conduct in-depth literature reviews and gather relevant scientific data from peer-reviewed journals, databases, and clinical reports.
  • Analyze and synthesize scientific information to prepare well-structured documents, including research summaries, manuscripts, white papers, and regulatory content.
  • Collaborate with scientists, subject matter experts, and cross-functional teams to ensure accuracy, clarity, and consistency of written materials.
  • Prepare data-driven reports and presentations for internal and external stakeholders.
  • Ensure compliance with scientific, ethical, and regulatory writing standards (, ICH, GCP, CONSORT, or similar).
  • Stay updated with current developments in life sciences, healthcare, and biotechnology sectors.
  • Requirements:
  • Master's or PhD in Life Sciences, Biotechnology, Pharmacy, Medicine, or related field.
  • Proven experience in scientific/medical writing or research analysis.
  • Strong ability to critically analyze data and translate complex concepts into clear, concise narratives.
  • Proficiency with scientific databases (PubMed, Embase, Scopus, etc.) and reference management tools (EndNote, Mendeley, Zotero).
  • Excellent written and verbal communication skills with attention to detail.
  • Familiarity with statistical analysis and clinical trial design is a plus.
  • Ability to work independently, manage deadlines, and handle multiple projects.
  • What We Offer:
  • Opportunity to work on impactful projects in the life sciences and healthcare sector.
  • A collaborative environment with scientists, researchers, and industry experts.
  • Professional development and training in scientific writing and research methodology.
  • Competitive compensation package with growth opportunities.

  • This advertiser has chosen not to accept applicants from your region.
     

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