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2.0 - 6.0 years
0 Lacs
hyderabad, telangana
On-site
As a Regulatory Medical Writer-Clinical trials (RMW-CT), you will be responsible for providing regulatory affairs (RA) strategic document expertise and support to one or more therapeutic areas (TAs) as designated by leadership. Your role will involve supporting the preparation and submission of critical RA documents and responses to health authority (HA) or sponsor information requests using available reference materials. You may lead interactions with sponsors or designated HAs, contributing to the preparation of submission materials, and ensuring the accuracy and quality of submission-ready documents. Additionally, you will partner with sponsor/HAs leadership to prepare high-quality, accur...
Posted 1 week ago
3.0 - 7.0 years
0 Lacs
kanchipuram, tamil nadu
On-site
**Role Overview:** You will be a part of the team at STM Journals, collaborating with researchers to support the publication of impactful scientific discoveries. Your focus will be on rigorous peer review, ethics, and reproducibility. As a key member of the team, you will actively contribute to advancing science, improving health outcomes, and promoting equitable participation in publishing. **Key Responsibilities:** - Analyze concerns in manuscripts flagged by Elsevier's research integrity technology solution to validate signals or resolve false positives. - Decide, following protocols, which concerns can be addressed by authors before reconsideration. - Review manuscripts where concerns ha...
Posted 3 weeks ago
1.0 - 5.0 years
0 Lacs
kanchipuram, tamil nadu
On-site
As a Publishing Ethics Analyst within Elsevier's Science, Technology and Medical Journal (STMJ) publishing division, your role will involve strengthening the team by providing support and advice to Ethics Experts, Editors and Publishers in coordinating and handling ethical allegations primarily related to published content. You will play a crucial part in nurturing and upholding research integrity within the journals and the broader research community. Your responsibilities will include: - Communicating with authors, reviewers, editors, and publishing teams regarding allegations of unethical behavior in a precise and diplomatic manner - Gathering and sharing insights to propose changes to ed...
Posted 3 weeks ago
8.0 - 12.0 years
0 Lacs
hyderabad, telangana
On-site
As a Systems Integration Advisor at NTT DATA, your role will involve utilizing your 8+ years of hands-on development experience to work independently and collaboratively within a team. Your key responsibilities will include: - UI Development using Angular/ React JS, Bootstrap, jQuery, Ajax, CSS, JS - Building .Net Core MVC REST APIs with micro services architecture - Utilizing CICD tools like Azure DevOps, Jenkins, Git, JIRA etc. - Demonstrating strong SQL Server expertise including DML, DDL, and Stored procedures - Exposure to Agile, Peer-review, and Test-Driven Development (TDD) - Experience in maintaining AWS/Azure Infrastructure such as setting up load balancers, creating IAM policies, m...
Posted 2 months ago
0.0 - 4.0 years
0 Lacs
pune, maharashtra
On-site
At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture, and technology to become the best version of you. And we're counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. As a global leader in Assurance, Tax, SAT, and Consulting, EY is using the finance products, expertise, and systems developed to build a better working world. This begins with a culture that believes in providing training, opportunities, and creative freedom to make things better. The exceptional EY experience lasts a lifetime, offering a co...
Posted 4 months ago
3.0 - 7.0 years
0 Lacs
chennai, tamil nadu
On-site
RRD GO Creative is seeking experienced Medical Writers to join our team in Chennai. In this role, you will play a crucial part in developing high-quality and scientifically accurate medical and regulatory documents, such as clinical study reports, protocols, and brochures. Your responsibilities will also include creating clear and concise medical content tailored for healthcare professionals, regulatory agencies, and internal stakeholders. To excel in this role, you must conduct thorough research and literature reviews to ensure content accuracy and compliance with industry standards. Collaborating with subject matter experts, scientists, and regulatory teams is essential to develop compelli...
Posted 5 months ago
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