Clinical Trials Jobs in Panchkula
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Search Results - Clinical Trials Jobs in Panchkula
Signant Health-Panchkula
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...
princeps technologies-Panchkula
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...
SIRO-Panchkula
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...
Cytel-Delhi, 230 km from Panchkula
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 valuesWe...
Qinecsa Solutions-Panchkula
Registration
Experience: 1 - 3 years in Pharmacovigilance
Primary Responsibilities
As a medical reviewer
• Conduct review and assessment of individual case safety reports obtained from clinical trials, spontaneous and solicited reports
• Determine...
iqvia india-Delhi, 230 km from Panchkula
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...
Valos Srl-Panchkula
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...
ACL Digital-Chennai, 1989 km from Panchkula
Identifies out of scope tasks and escalates to management.
• Ensure compliance with regulatory guidelines and industry standards
• Prepare and review clinical trial reports, and regulatory submissions.
• Mentor and provide guidance to junior statistician...
Cytel-Panchkula
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...
Cytel-Panchkula
that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
Responsibilities
As a Principal Statistical Programmer, your...
CloudLabs Inc-Panchkula
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...
Veramed-Panchkula
Brief Description:
The Principal Biostatistician will be responsible for performing and validating statistical analyses in support of the clinical trial portfolio, in accordance with departmental SOP and guidelines, as needed and sit within...
Imaging Endpoints-Panchkula
that are passionate in their desire to assist us in our mission to customize each clinical trial’s imaging to optimize the opportunity to demonstrate efficacy.
Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; London, UK...
vueverse.-Panchkula
Senior Statistical Programmer
Experience: 6–12 Years
Location: Hyderabad
Role Overview
The Senior Statistical Programmer will support clinical trial programming activities including SDTM, ADaM dataset development and TLF programming...
MasterControl-Panchkula
new levels of operational excellence across product development, clinical trials, regulatory affairs, quality management, supply chain, manufacturing and postmarket surveillance. For more information, visit www.mastercontrol.com.
Role
Design and own...
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