Clinical Trials Jobs in Vellore
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Search Results - Clinical Trials Jobs in Vellore
ProductLife GroupVellore
Experience
Doctor or pharmacist by training
Minimum 4 years experience working for service providers performing QC of case
Minimum 3 years of experience in processing Clinical Trial cases.
SafetyEasy/ Argus database experience
Profile
Database experience...
Safeguard Global RecruitingVellore
and implementation of project management methodologies and processes.
Responsibilities
• 3-5 years industry experience including at least 1 year in Project Management roles in clinical trials within a CRO, pharmaceutical or biotech setting.
• Good knowledge...
Safeguard Global RecruitingVellore
management principles, methodologies, and processes
KEY SKILLS, KNOWLEDGE AND QUALIFICATIONS REQUIRED: At least 2 years’ experience working in clinical trials.
Demonstrable experience in the management or coordination of clinical trials, ideally gained...
CytelVellore
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...
Safeguard Global RecruitingVellore
roles in clinical trials within a CRO, pharmaceutical or biotech setting'
Good knowledge of the drug development process, associated regulatory and ICH GCP guidelines and their application to clinical trials.
Detailed and proactive approach to risk...
CytelVellore
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...
Teamware SolutionsVellore
experience within pharmaceutical clinical development - Supporting regulatory filings (e.g. NDA, BLA, MAA)
• Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements
• Experience...
VeramedVellore
Purpose:
This function supports the protection of patient privacy when clinical trial data is shared externally.
Typical use cases:
• Regulatory submissions
• Data sharing with researchers
• Health authority requests
• External collaborations...
Letstream ®Vellore
Immediate — expected start between the second and third week of September 2026
About the role
You'll be building and maintaining an eCOA (electronic Clinical Outcome Assessment) solution used in clinical trials. The product captures assessment data from...
Safeguard Global RecruitingVellore
on Protocol and CSR projects across all clinical trial phases and a variety of therapeutic areas.
• Passion for science and healthcare.
• Excellent computer skills including knowledge of Adobe, Internet software, Spreadsheet software, Word Processing software...
Imaging EndpointsVellore
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...
ACL DigitalVellore
Statistical Programmer of Statistical Programming is responsible for all statistical programming aspects of one or more clinical trials of drug development plans. The position ensures drug development plans are executed efficiently, with timely and high...
VeramedVellore
of CDISC standards, and experience supporting NDA/BLA/MAA submissions.
Key Responsibilities:
• Lead statistical programming activities for ISS/ISE analyses and pooled clinical trial datasets.
• Design, develop, validate, and maintain integrated ADaM...
DAVA OncologyVellore
to: clinical trial research and communications, drug or trial publication research and review, and oncology conference meeting reviews. Candidates with previous experience in the oncology therapeutic area are highly desirable.
Responsibilities:
• Conduct...
IQVIAVellore
if working knowledge with R software.
• Min. 3 years industry experience.
• Strong working knowledge of R software (important)
• Interest in PK/PD and clinical trial concepts.
• Studious and data driven person. Eye for detail is very important.
• Proficient...
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