Global Clinical Publishing Associate
21 hours ago
Summary Ensure compliance with internal and external guidelines to compile and add electronic navigation to clinical and regulatory documents Support the timely submission of documents to the Health Authorities HAs and provide publishing consultancy to the clinical teams and other line functions Key Responsibilities In collaboration with the clinical teams compile integrate and publish clinical documents with word processing electronic publishing and document management systems in the Novartis Development environment Perform technical quality control electronic functionality adherence to internal and external document standards of published documents Maintain basic knowledge of current electronic publishing standards regulatory guidelines and legal requirements Under direct supervision of the immediate manager acts as the Program Publisher for various programs in clinical development Publish clinical documents taking into account complexity and size in accordance with department standards and organization KPIs Ensure published clinical documents meet current internal and external quality standards for electronic and or paper HA submissions including minimizing publishing-related technical QC findings and no rework once finalized Timeliness of deliverables meet both individual document and overall project timelines Minimum Requirements 3-5 years submission publishing experience in Pharma or related industry Experience with regulatory submission format including familiarity with submission publishing activities and CTD format criteria Effective interpersonal skills strong written and oral communication and presentation skills Project management and time management skills to manage multiple ongoing projects simultaneously Familiar with regulatory requirements and HA guidances including FDA regulations ICH and EMA guidelines directives Working knowledge of regulatory affairs works independently and with minimal supervision Proficiency with computer programs systems MS office etc with demonstrated ability to learn new systems quickly Analytical skills and problem solving skills ability to coordinate and work effectively with cross-functional teams Commitment to Diversity and Inclusion Novartis is committed to building an outstanding inclusive work environment and diverse teams representative of the patients and communities we serve Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities If because of a medical condition or disability you need a reasonable accommodation for any part of the recruitment process or in order to perform the essential functions of a position please send an e-mail to diversityandincl india novartis com and let us know the nature of your request and your contact information Please include the job requisition number in your message Skills Desired Analytical Skill Clinical Trials Collaboration Detail-Oriented Lifesciences Project Planning Regulatory Compliance
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Global Clinical Publishing Associate
5 hours ago
Hyderabad, Telangana, India Novartis Full time**Summary**: Ensure compliance with internal and external guidelines, to compile and add electronic navigation to clinical and regulatory documents. Support the timely submission of documents to the Health Authorities (HAs) and provide publishing consultancy to the clinical teams and other line functions. **About the Role**: **Major accountabilities**: -...
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Global Clinical Publishing Associate
2 days ago
Hyderabad (Office), India Novartis Full time ₹ 40,00,000 - ₹ 80,00,000 per yearJob Description SummaryEnsure compliance with internal and external guidelines, to compile and add electronic navigation to clinical and regulatory documents. Support the timely submission of documents to the Health Authorities (HAs) and provide publishing consultancy to the clinical teams and other line functions.Job DescriptionMajor accountabilities: In...
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Global Clinical Publishing Associate
5 hours ago
Hyderabad (Office), India Novartis Full time ₹ 12,00,000 - ₹ 36,00,000 per yearBandLevel 3Job Description SummaryEnsure compliance with internal and external guidelines, to compile and add electronic navigation to clinical and regulatory documents. Support the timely submission of documents to the Health Authorities (HAs) and provide publishing consultancy to the clinical teams and other line functions.Job DescriptionMajor...
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Global Reg Sub Publishing Associate
4 days ago
Hyderabad, India Novartis Full time26 major approvals. 13 major submissions. 2,000 associates worldwide. That was Regulatory Affairs in 2020. We are a culturally diverse, global team of talented professionals seeking to leverage the voices of our patients in our approach to bringing potentially life-changing therapies to people who need them. Novartis has a robust pipeline, including possible...
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Global Trial Acceleration Associate
2 weeks ago
Hyderabad, Telangana, India Bristol-Myers Squibb Full time**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
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Global Trial Acceleration Associate
2 weeks ago
Hyderabad, Telangana, India Bristol-Myers Squibb Full time**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms...
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Associate Clinical Study Manager
5 days ago
Hyderabad, Telangana, India Novartis Full timeSummary LI-Hybrid Location Hyderabad India Step into a role where your expertise drives innovation in clinical research As an Associate Clinical Study Manager you ll play a pivotal part in shaping the future of patient care by ensuring our studies are executed with precision quality and compassion At Novartis your contributions will directly impact lives and...
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Clinical Research Associate
1 week ago
Greater Hyderabad Area, India Admerus Biosciences Private Limited Full time ₹ 8,00,000 - ₹ 12,00,000 per yearCompany DescriptionAdmerus Biosciences, headquartered in Hyderabad, India, is a Contract Research Organization (CRO) that services the global Biopharma industry. We partner with reputed global biopharma and research laboratories to find efficient, cost-effective, and innovative solutions to their clinical development challenges. Our focus is on delivering...
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Apprentice - Editorial, Design & Publishing
6 days ago
Hyderabad, Telangana, India S&P Global Full timeApprentice - Editorial, Design & Publishing **About the Role**: **Grade Level (for internal use)**: 05 **The Role**: We are looking for an apprentice for a period of **12-months** in our **Editorial, Design & Publishing** Team, responsible for branding and editorial support on S&P Global Market Intelligence content. The main focus is to maintain and enhance...
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Veeva Ectd Bla Publisher
6 hours ago
Telangana, India Zensar Technologies Full time**Key Responsibilities**: - Prepare, compile, and publish **Biologics License Application (BLA)**submissions in **eCTD format**using **Veeva Vault**and other publishing tools. - Format regulatory documents (PDFs) in compliance with **ICH and regional specifications**, including **bookmarks, hyperlinks, metadata**, and file naming conventions. - Perform...