Clinical Documentation jobs
Explore 95 current openings. Compare roles, companies, locations, and work options, then open any job to view the full details.
Current openings
Showing 20 jobsClinical Document Management Specialist
OraClinical Document Management at Ora builds the future of ophthalmic clinical research by ensuring every trial document is accurate, compliant, and ready for inspection. The specialist manages the eTMF in Veeva Vault, …
Hyderabad,IndiaOn-siteFull-timeActiveClinical Document Specialist
NovotechClinical Document Specialist supports Trial Master File activities, ensuring quality and compliance with SOPs, regulatory guidelines, and eTMF systems. Responsible for document upload, QC, process improvement, training, …
IndiaOn-siteFull-timeActiveGlobal Clinical Publishing Associate
NovartisEnsure compliance with internal and external guidelines, compile and add electronic navigation to clinical and regulatory documents, support timely submission to Health Authorities, provide publishing consultancy to …
Hyderabad, IndiaOn-siteFull-timeActiveAssociate Director, Non
AstraZenecaRegulatory Operations team at AstraZeneca India leads a specialist group that ensures high‑quality regulatory submissions, focusing on SEND data document management, archiving, and the Submission Ready Standard (SRS). …
Bangalore,IndiaHybridFull-timeActiveMedical Documents Filing/Abstract / Medical documentation/ Medical records
ARstratMedical Documents Filing/Abstract team at ARstrat focuses on organizing and indexing scanned medical records to support clinical workflows. The role maintains a structured filing system, assigns file names, folders, and …
Bangalore,IND,IndiaFull-timeActiveGlobal Clinical Publishing Associate
NovartisThe Global Clinical Publishing Associate ensures compliance with guidelines, compiles and adds electronic navigation to clinical and regulatory documents, and supports timely submissions to Health Authorities. The role …
Hyderabad (Office)Full timeActivePrincipal Medical Writer
GSKPrincipal Medical Writer at GSK responsible for independently drafting, reviewing, and approving complex clinical documents for regulatory submissions worldwide. The role requires a PhD in life sciences and at least …
Bengaluru, IndiaOn-siteFull-timeActiveDocument Controller
SURBANADocument Controller at Surbana Jurong India Private Limited manages and maintains all project documents, ensuring proper version control and compliance with documentation standards. The role coordinates with engineers, …
Ahmedabad,IndiaOn-siteFull-timeActiveDocument Anonymization Specialist
GSKDocument Anonymization Specialist at GSK leads the anonymisation of clinical documents to support ethical data sharing. The role manages regulatory compliance, vendor relationships, and daily operations of document …
Bengaluru,IndiaOn-siteFull-timeActiveDocument Controller
WSPDocument Controls team at WSP ensures accurate creation, storage, and distribution of project documentation across infrastructure projects. The role establishes and maintains document control systems, conducts audits …
Noida, Uttar Pradesh, IndiaHybridFull-timeActiveSenior Manager, Clinical Scientist
Bristol-Myers Squibb CompanySenior Manager, Clinical Scientist at Bristol‑Myers Squibb leads cross‑functional teams to develop and monitor clinical protocols, conduct literature reviews, and produce regulatory documents. Responsibilities include …
Hyderabad, TS, IndiaOn-siteFull-timeActiveDocument Controller
KBRDocument Controller at KBR in Gurgaon, India, responsible for maintaining project documentation files, including technical data, engineering and supplier drawings, and specifications. The role processes, numbers, files, …
Gurgaon,IndiaOn-siteFull-timeActiveClinical Research Associate I
AbbottClinical Research Associate I at Abbott supports site management and regulatory compliance across clinical trials in India. Responsible for collecting and reviewing essential regulatory documents, maintaining trial …
Gurgaon, IndiaOn-siteFull-timeActiveDocument Controller
WSPDocument Controls team at WSP supports UK Mining operations by managing project documentation and ensuring compliance with company procedures. The role handles storage, upload/download, and workflow of documents using …
Bengaluru,Karnataka,IndiaHybridFull-timeActiveClinical Research Associate I
AbbottClinical Research Associate I supports site management and regulatory compliance for Abbott clinical trials in India. Works with US and EMEA teams to collect, review, and upload essential regulatory documents, ensuring …
Gurgaon, IndiaOn-siteFull-timeActiveDocument Controller
GE VernovaDocument Control Team at GE Vernova ensures project documentation is accurate, up‑to‑date, and accessible throughout the project lifecycle, supporting quality and process improvement initiatives. The role maintains and …
Noida,IndiaOn-siteFull-timeActiveClinical Publishing Coordinator
LabCorpLabcorp’s Clinical Publishing Coordinator at Brigade Twin Towers, Yeshwanthpur, Bangalore, supports the creation and modification of clinical investigator manuals, requisitions and other documentation to meet SOW …
Bengaluru,IndiaOn-siteFull-timeActiveDocument Controller
LARSEN & TOUBRO LTD.Document Management team at Larsen & Toubro Ltd. oversees electronic and hard copy documentation for the Hydrocarbon Offshore division. The role ensures documents are accurately categorized, stored, backed up, and …
Powai,Maharashtra,IndiaOn-siteFull-timeActiveClinical Publishing Coordinator
LabCorpLabcorp’s Clinical Publishing Coordinator at Brigade Twin Towers, Yeshwanthpur, Bangalore, drives the creation and modification of clinical investigator manuals, requisitions and other documentation to meet SOW …
Bengaluru,IndiaOn-siteFull-timeActiveDocument Specialist
ProPharma GroupProPharma Group seeks a Document Specialist to support regulatory document preparation and eCTD publishing for clients in the pharmaceutical and biotech sectors. The role involves formatting, reviewing, and converting …
Hyderabad, IndiaOn-siteFull-timeActive