Average salary: Rs563,484 /yearly
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Rs 2.5 - 5 lakhs p.a.
Technical Script Writer Start Date Starts Immediately CTC (ANNUAL) ₹ 2,50,000 - 5,00,000 ₹ 2,50,000 - 5,00,000 /year ...SuggestedRemote jobFull timeInternshipImmediate startWork from homeWorking Monday to Friday- ...Engineering FRQ Type: Contract Compensation: $85/hour Location: Remote Role Responsibilities Author original, free-response engineering problems in Materials Science & Engineering . Develop expert-level solutions grounded in real...SuggestedRemote jobContract workSummer work
- ...Clinical Publications Author Contract · Remote Annual Compensation Equivalent: $104,000–$166,400/year About the Role We’re looking for experienced clinical and medical publications professionals who can bring strong scientific judgment, publication expertise, and...SuggestedContract workRemote job
- ...Content Author Job Description The Content Author is an entry point into the content team's career path, combining hands-on content authorship with full ownership of the content production process. This role analyzes source material from multiple resources and writes,...SuggestedFull timeHybrid workWork at officeFlexible hours
- ...Compensation: $61–$77/hour Location: Remote Commitment: 10+ hours/week Role Responsibilities Author original physics questions that test deep conceptual understanding. Ensure questions are unambiguous, self-contained, and precisely defined...SuggestedRemote jobContract workSummer work
- Fortrea seeks a Medical Writer to prepare and review clinical documents including patient safety narratives and clinical study report appendices. The role involves supporting senior medical writers with protocol and CSR preparation while ensuring compliance with regulatory ...Suggested
- ...deliveries to Medical, HEVA, and Commercial organizations in Sanofi, globally. Main responsibilities: Responsible for research and authoring of scientific response documents under the direction of the Global Medical Information (GMI) team in support of global and local...SuggestedLocal area
- Key Responsibilities Write and edit white papers, research articles and long-form technical content & create blogs and articles on our technology, its applications and wider industry trends. Translate complex technical information into clear, accessible content for ...SuggestedFull time
- ...platform is designed to execute complex revenue-cycle workflows across areas such as eligibility and benefits verification, prior authorization, claims processing, denial management, accounts receivable and revenue integrity. The company works at the intersection of Artificial...Suggested
- In 2018, we began with a WhatsApp group with a simple hypothesis: people in tier-2/3 towns weren’t really using the internet meaningfully yet. We believed that if we started with local content in their own language, they’d come back every day; once there was a habit and...SuggestedContract workLocal area
- About Parexel Parexel is a leading global clinical development partner delivering insights-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design...SuggestedHybrid workRemote jobWorldwide
- PK Medical Writer At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment...SuggestedRemote jobContract workLocal areaWorldwideFlexible hours
Rs 25000 - Rs 35000 per month
Job Title:Technical Content Writer Location: Ahmedabad Type: Full-Time Experience Level: 2 to 3 Years Unleash Your Words at SolGuruz: Craft Your Future as a Technical Content Writer! Are you a wordsmith with a passion for weaving ideas into captivating narratives...SuggestedFull timeContract workFlexible hours- This is a remote position. About MTechZilla MTechZilla is a web, mobile app, AI app, and cloud app development agency based in India, serving as an offshore engineering partner for US and EU companies. We work with US and EU engineering teams through three flexible...SuggestedFull timeCasual workRemote jobFlexible hours
Rs 3.6 - 4.2 lakhs p.a.
Technical Content Writer Start Date Starts Immediately CTC (ANNUAL) ₹ 3,60,000 - 4,20,000 ₹ 3,60,000 - 4,20,000 /year ...SuggestedImmediate startWorldwideRs 2 - 5 lakhs p.a.
Technical Content Writer Start Date Starts Immediately CTC (ANNUAL) ₹ 2,00,000 - 5,00,000 ₹ 2,00,000 - 5,00,000 /year ...Local areaImmediate start- ...guidance to colleagues and supporting continuous improvement across the function. What You'll Do Medical Writing & Document Development - Author, review, and quality-check a range of regulatory and scientific documents, including clinical study reports and other medical writing...Full timeWorldwide
Rs 3 - 5 lakhs p.a.
We are seeking a highly motivated and results-driven Financial Script Writer with experience in writing about the financial market and a passion for writing in the financial services industry. The ideal candidate will have at least 2-5 years of experience in a similar role ...- In 2018, we began with a WhatsApp group with a simple hypothesis: people in tier-2/3 towns weren’t really using the internet meaningfully yet. We believed that if we started with local content in their own language, they’d come back every day; once there was a habit and...Local area
- Intern – Technical Content Writer (Marketing) We are looking for a creative and research-oriented Technical Content Writer Intern to support our marketing team in developing compelling content for websites, social media, blogs, and other marketing initiatives. The ideal...Full timeInternship
- ...the company stronger. For more information, visit or follow MMS on LinkedIn . Job Responsibilities Act as a project lead and author clinical development documents, including but not limited to, clinical protocols, investigator’s brochures, clinical study reports, subject...Remote jobFull timeWorldwideFlexible hoursShift work
- Medtronic seeks a Clinical Evaluation Medical Writer to develop and maintain regulatory documents for medical devices, including Clinical Evaluation Reports and Safety summaries. The role involves analyzing clinical data, managing regulatory submissions, and ensuring compliance...
- ...redaction/anonymization packages, anonymization reports, and CCI justification tables Advanced clinical and regulatory document authoring and review expertise, including Study Protocols, Clinical Study Reports (CSRs), Investigator Brochures (IBs), Informed Consent Forms...Remote jobWorldwide
$ 57600 p.a.
...availability, and engagement duration. About the Role We’re seeking experienced Pharmaceutical Medical Writers and Clinical Document Authors to contribute to the development and evaluation of AI-assisted tools for clinical and regulatory documentation. You’ll apply...40 hours per weekFull timeContract workFor contractorsRemote jobRs 2 - 6 lakhs p.a.
Actively hiring Technical Content Writer (AI, SEO, AEO, GEO) Start Date Starts Immediately CTC (ANNUAL) ₹ 2,00,000 - 6,00,000 ₹ 2,00,000 - 6,00...Full timeImmediate startRs 3.5 - 4.5 lakhs p.a.
Script Writer Start Date Starts Immediately CTC (ANNUAL) ₹ 3,50,000 - 4,50,000 ₹ 3,50,000 - 4,50,000 /year Experience...FreelanceImmediate start- ...documentation standards, including ATA iSpec 2200, S1000D, and ASD-STE100 (Simplified Technical English). Experience with technical authoring and publishing tools such as Arbortext Editor, Arbortext Publishing, and Adobe FrameMaker. Familiarity with technical...Full time
- Responsibilities Write, edit, and proofread documents for different departments. Develop product user handbooks, technical descriptions, overhaul and maintenance manuals, design specifications, and other technical documentation. Create requests for proposal (RFPs) ...Full time
- Secure Every Identity, from AI to Human Identity is the key to unlocking the potential of AI. Okta secures AI by building the trusted, neutral infrastructure that enables organizations to safely embrace this new era. This work requires a relentless drive to solve complex...Full timeHybrid workWork at officeLocal areaWorldwide2 days week
- ...compliance, and liaises between scientific, quality, and regulatory teams. Responsibilities Coordinate scientific input from multiple authors, reviewers, and subject matter experts Track document components through drafting, review, and approval stages Ensure...