Clinical Trials Jobs in Tumkūr
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Search Results - Clinical Trials Jobs in Tumkūr
Apsida Life Science-Tumkūr
Title : Clinical Trial Regulatory Submission SME
Location : India (Remote)
Contract Duration : 6–12 months
Hours: Up to 150 hours/month
Working Hours : EU/UK-aligned working hours may be required
Start Date : ASAP
Company Overview:
Apsida Life...
ProductLife Group-Tumkūr
Education & 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...
Proxima Skills Academy-Tumkūr
to Training and Clinical Trials processes, with willingness to learn standard clinical documentation practices.
Attention to detail, accuracy in data entry, and ability to follow structured workflows and guidelines.
Bachelor’s degree in Life Sciences, Pharmacy...
Proxima Skills Academy-Tumkūr
will support clinical data review and data validation activities to ensure accuracy, completeness, and consistency of clinical trial data. Daily responsibilities include performing data checks against study protocols, documenting and resolving data...
Proxima Skills Academy-Tumkūr
possess skills in study design and conduct, including Protocol and Clinical Trials.
Candidates should possess skills related to participant engagement and ethics, including Informed Consent.
Relevant educational background in Life Sciences, Pharmacy...
Safeguard Global Recruiting-Tumkūr
of project 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...
Cytel-Tumkūr
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 Recruiting-Tumkūr
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...
Cytel-Tumkūr
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...
Ephicacy-Tumkūr
Experience: 6-10 years
🔹 Location: PAN India
🔹 Work Mode: Full-Time | Remote
🔬 Key Requirements
We are looking for candidates with strong hands-on experience in:
✅ End-to-End SAS Programming in Clinical Trials
✅ ADaM and TLF development...
Ayur.AI-Chennai, 345 km from Tumkūr
Description
We are seeking a highly organized and proactive Clinical Research Intern to support the daily operations of our longitudinal clinical trials. The study involves Continuous Glucose Monitoring (CGM), lab testing, gut microbiome analysis, and remote...
Syneos Health-Tumkūr
in a clinical trial environment.
Excellent written and verbal communication skills.
Ability to read, write, speak and understand English.
Email your CV on:
Veramed-Tumkūr
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...
IQVIA-Tumkūr
experience in developing and reviewing Data Validation Listings.
Good understanding of clinical trial data and programming standards.
Working knowledge of SAS Macros and SQL.
Strong analytical, problem-solving, and communication skills.
Demonstrated...
Veramed-Tumkūr
listed below outline the scope of the position. The application of these tasks may vary, based on current business needs.
Responsibilities
Technical: Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs
Author...
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