Clinical Trials Jobs in Pune
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Search Results - Clinical Trials Jobs in Pune
AIXIAL GROUP-Pune
in the clinical research industry, supporting biotech in clinical trials across all phases (Ph. I - IV) and non-interventional studies, as an expert in the operational delivery of clinical trials. Our vision is to conduct clinical trials better than anyone else...
Triomics-Pune
At Triomics, we are creating the future of clinical trials. We are a technology-driven
clinical trial partner running faster, cost-effective, and transparent clinical trials across
the globe. Our proprietary eSource and direct-to-patient...
TransPerfect-Pune
Experience with essential documents and other study documentation.
• Experience with clinical trials at research sites, IRB submissions, pharmacovigilance is a plus.
Desired Skills and Experience:
• Previous employment in Pharmaceutical, CRO, Medical Device...
CliniLaunch Research Institute-Pune
Job Description
Skills:
Clinical Research, Clinical, Research, CR, Pharmacovigilance, Regulatory Affairs, Clinical Trials,
As a Senior CRA, you will participate in the preparation and execution of Phase I-IV clinical BA/BE studies...
foundit.in -
TransPerfect Solutions India Pvt. Ltd.-Pune
OVERVIEW
The eClinical Systems Analyst has good knowledge of clinical trial processes and associated systems utilized. With core skills around Trial Master File (TMF) processes they work as support to Study Owners to ensure a complete...
USV PRIVATE LIMITED-Pune
Review of clinical trial and bioavailability and bioequivalence clinical study protocols, Literature
search, relevant study documents such as CRF, ICF etc and Clinical study report (eCTD) including
appendices.
• Review of documents such as Clinical...
Trigent Software Inc-Pune
SummaryA Clinical Research Associate (CRA) is responsible for monitoring and managingclinical trials to ensure compliance with regulatory guidelines, Good Clinical Practice(GCP), and study protocols. The CRA serves as the primary point of contactbetween...
princeps technologies-Pune
cutting-edge solutions to support clinical trial data analysis and regulatory submissions. Key Responsibilities: Develop and maintain global R codebase for generating CDISC ADaM datasets and tables, listings, and figures in accordance with clinical trial...
Capgemini-Pune
processes in manufacturing, clinical trials, quality control, and laboratory settings.
Lead the organization’s compliance with Sarbanes-Oxley (SOX) Act, focusing on internal controls over financial reporting, documentation, and audit readiness.
Develop...
Ephicacy-Pune
Key Responsibilities Develop and maintain global R codebase for generating CDISC Adam datasets and tables, listings, and figures in accordance with clinical trial data requirements Ensure compliance with industry standards and regulatory...
TransPerfect-Pune
The Team consists of TMF Managers and supporting TMF analysts, who are embedded in Clinical Trial Teams (CTTs) and covers Inhouse and outsourced studies (which also includes Full-Service Outsourcing Model (FSOM) studies those as part of Business...
Excelya-Pune
Excelya is one of the leading CROs in Europe, founded in 2014 and headquartered in Paris. Our global team is composed of 900+ experts who understand the critical needs of clients and provide trial solutions across a broad spectrum of therapeutic...
TransPerfect-Pune
The Team consists of TMF Managers and supporting TMF analysts, who are embedded in Clinical Trial Teams (CTTs) and covers Inhouse and outsourced studies (which also includes Full-Service Outsourcing Model (FSOM) studies those as part of Business...
Fortrea-Pune
Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process, which may include safety data collected from clinical trials and/or post marketing settings (i.e., unsolicited reports...
foundit.in -
USV PRIVATE LIMITED-Pune
of clinical trial and bioavailability and bioequivalence clinical study protocols, Literaturesearch, relevant study documents such as CRF, ICF etc and Clinical study report (eCTD) includingappendices. Review of documents such as Clinical overview and Non...
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