Clinical Research Clinical Data Management Sas Jobs

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Senior SAS Programmer/Lead Programmer - CRO/Pharmaceutical  

ApicalGo Consultancy - India, IN

resolution of data problems. The Clinical Programmer typically creates programs using SAS to support the clinical research projects. RESPONSIBILITIES : - Collaborate with statistician and other functions

from: adzuna.in (+1 source) - 6 days ago

Principal Stats Programmer  

Fortrea - All India (+1 location)

of the roles and responsibilities of all related disciplines, e.g., Biostatistics and Clinical Data Management. Broad knowledge of all CDISC requirements related to SDTM and ADaM, including define.xml

from: Shine.com (+1 source) - 26 days ago

Business Development Manager  

Biosphere Clinical Research Pvt Ltd - Thane, India

, clinical data management, and SAS data extraction services to sponsors and CROs. With over 600 investigators and a strong patient database, we conduct Phase II, Phase III, and Phase IV Clinical Trials Not Mentioned

from: Monsterindia.com - 18 days ago

Manager - Clinical Data Programming  

Bioclinica - Remote, India (+1 location)

+ years experience as a SAS programmer, including use of the SAS Macro facility Previous data management experience in pharmaceutical research and development required 5+ years clinical trials experience Not Mentioned

from: Monsterindia.com - More than 30 days ago

Executive Director - Clinical Technology Platforms (Safety & Data Sciences)  

Fortrea - Bengaluru / Bangalore, India

, in safety, biostatistics, data management, and pharmacology within the pharmaceutical, biotechnology, or Clinical Research industry At least 5 years of experience in a leadership role Experience with typical Not Mentioned

from: Monsterindia.com - 22 days ago

Clinical Data Manager  

EMentor Enterprises Private Limited - Hyderabad / Secunderabad, Telangana, India

, Computer Science, or related field. Proven experience in clinical data management in a pharmaceutical or CRO environment. Strong knowledge of data management practices and regulatory guidelines (e.g., GCP Not Mentioned

from: Monsterindia.com - More than 30 days ago

Clinical Data Manager  

EMentor Enterprises Private Limited - Hyderabad / Secunderabad, Telangana, India

in clinical data management in a pharmaceutical or CRO environment. Strong knowledge of data management practices and regulatory guidelines (e.g., GCP, ICH). Proficiency in data management software and tools Not Mentioned

from: Monsterindia.com - 22 days ago

Senior Clinical Data Analyst  

myGwork - LGBTQ Business Community - Hyderabad / Secunderabad, Telangana, India

required. Skills Good understanding of Clinical Study Team roles within Data Management - awareness of DML activities e.g.: budget reviews, resource forecast, etc. Experience in clinical research industry Not Mentioned

from: Monsterindia.com - 21 days ago

Business Analyst  

Eclinical Solutions - Bengaluru / Bangalore, India

in the life sciences technology industry, particularly clinical trials in a role such as a clinical research associate, data manager, or similar role. Professional Skills: Excellent writing skills, able Not Mentioned

from: Monsterindia.com - 12 days ago

Urgent Openings for EDC Veeva Programmer : Salary - 30 LPA + NSA : Location - Bangalore & Mumbai  

Job World - Bengaluru / Bangalore, Mumbai, Mumbai City, Navi Mumbai, Thane

. • Minimum of 4+ years' experience in Data Management, Programming, Clinical IT, or other Clinical Research related fields. • Hands-on experience with at least one EDC system (e.g.: Medidata Rave, Inform Not Mentioned

from: Monsterindia.com - 22 days ago


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