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Clinical Trials Jobs in Delhi

1 - 15 of 32
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1 - 15 of 32
Search Results - Clinical Trials Jobs in Delhi
Signant Health-Delhi
About Signant Health At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational...
Cytel-Delhi
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.Our values We...
jmmst.com -
Signant Health-Delhi
About Signant Health At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational...
Crossdomain Solutions-Delhi
Registration Experience: 1 - 3 years in PharmacovigilancePrimary ResponsibilitiesAs a medical reviewerConduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports Determine regulatory...
jmmst.com -
SIRO-Delhi
Key Accountabilities: Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process Create edit check specifications and program or modify checks at study level within EDC Setup different instances...
Valos Srl-Delhi
ResponsibilitiesCreate ADAM and TFLs for clinical studiesApply advanced statistical methodologies to clinical trials and RWE studiesContribute to the development of Statistical Analysis Plans (SAPs) and study reportsCollaborate closely with cross-functional teams (data...
princeps technologies-Delhi
Job Title: Senior Statistical Programmer (Oncology) Location: Canada/IN Employment Type: Full-Time Experience: 8+ Overview We are seeking an experienced Senior Statistical Programmer with strong Oncology clinical trial experience to support end...
iqvia india-Delhi
of centralized monitoring activities to ensure subject safety, data integrity, regulatory compliance, and delivery of clinical trial objectives as per sponsor and contract requirements. The role partners with clinical, project, analytics, quality, and therapeutic...
jmmst.com -
Zydus Group-Delhi
Facilitate the understanding and dissemination of clinical trial data (company-sponsored and relevant external data).   5.  Training & Education:  •  Provide scientific and medical education to internal stakeholders (e.g., sales force, market access) on disease...
CloudLabs Inc-India
benefits, industry leading training.  •  Opportunity to work remotely is available. Experience Required: Medidata Rave, Custom Function Expert, Clinical Data Management. Minimum 2-3 years of relevant experience as Medidata Rave EDC programmer and strong...
Intertek India-Delhi
conducting performance testing, evaluation studies or clinical trials of the devices.  •  At least two (2) of the five (5) years shall be in the area of quality management.  •  Prior third-party auditing experience with a notified body is preferred.  •  Preferred...
Cytel-Delhi
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. Our values We...
vueverse.-Delhi
Senior Statistical Programmer Experience:6–12 Years Location:HyderabadRole Overview The Senior Statistical Programmer will support clinical trial programming activities includingSDTM, ADaM dataset development and TLF programmingin compliance...
jmmst.com -
Valos Srl-Delhi
Responsibilities Create ADAM and TFLs for clinical studies Apply advanced statistical methodologies to clinical trials and RWE studies Contribute to the development of Statistical Analysis Plans (SAPs) and study reports Collaborate closely with cross-functional...
Iqvia-Delhi
and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality, and company summary Compose, edit and medically review Analyses of Similar...
jmmst.com -
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