Clinical Trials Jobs in Bangalore
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Search Results - Clinical Trials Jobs in Bangalore
ClinoGenesis Research InstituteBangalore
Job Description – Clinical Trial Coordinator (CTC) | Hyderabad
About the Role
The Clinical Trial Coordinator (CTC) plays a key role in supporting the planning, initiation, execution, and close-out of clinical trials. This role involves...
ConnexRBangalore
that support clinical research, treatment outcomes, and healthcare decision-making. The ideal candidate should have experience working with clinical trials, EHR, claims data, and real-world evidence (RWE) and be skilled in statistical analysis, machine learning...
Biocon BiologicsBangalore
Job description:
Clinical Project Manager
1. Proactively manages clinical trials from start-up to closure with a focus on trial timelines, quality, budget, and vendor oversight.
2. Leads selection of CRO and vendors including identification...
ThermaissanceBangalore
innovation, and physician engagement.
Key Responsibilities
Clinical Study Development
• Design and coordinate clinical studies and pilot trials evaluating antimicrobial and thermoregulating textiles in:
• Neonatal intensive care units (NICU / SNCU)
• Adult...
MS CLINICAL RESEARCHBangalore
innovation and improving healthcare outcomes. We conduct high-quality clinical trials that adhere to global standards of excellence and contribute to the development of breakthrough medical solutions.
Job Summary
We are seeking an experienced and proactive...
Precision Medicine GroupBangalore
Degree, or equivalent experience ideally in a business, scientific or healthcare discipline
• 2 years' clinical trial experience with 2 years of experience with Clinical Systems
Other Required
• Experience in clinical trial systems (e.g., CTMS, EDC...
Rose InternationalBangalore
clinical research, healthcare, and life sciences roles (e.g., Clinical Research Associates, Clinical Data Managers, Regulatory Affairs Specialists, Clinical Trial Assistants, Pharmacovigilance Associates, etc.).
• Use niche clinical sourcing platforms...
Latinum HR SolutionsBangalore
for an experienced Statistical Programmer to oversee programming activities for clinical trials, regulatory submissions, and integrated analyses. This role involves leading a team, ensuring high-quality deliverables, and developing efficient programming standards...
TWO95 International, IncBangalore
R)
• Hands-on experience with statistical analysis and reporting in clinical trials
• Proficient in SAS and R for statistical modelling, efficacy analysis, and data interpretation
• Ability to collaborate closely with programming and clinical teams...
ThermaissanceBangalore
medical innovation, and physician engagement.
Key Responsibilities
Clinical Study Development
• Design and coordinate clinical studies and pilot trials evaluating antimicrobial and thermoregulating textiles in:
• Neonatal intensive care units (NICU...
Trigent Software IncBangalore
clinical trials (Phase 2/3 preferred) . The role involves data extraction, SDTM/ADaM programming, and TLG development , ensuring high-quality, submission-ready deliverables aligned with industry standards.Key ResponsibilitiesCreate and maintain SAS programs...
MS CLINICAL RESEARCHBangalore
Sciences, Pharmacy, Cosmetic Technology, or related field.
• 5–10 years of experience in clinical trials, with at least 2–3 years in a supervisory/managerial role.
• Experience in cosmetic/dermatology clinical studies is highly desirable.
Reporting...
CytelBangalore
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...
AlvotechBangalorefoundit.in
activities as medical reviewer of ICSRs, signal detection/evaluation, aggregate reports, and benefitrisk assessment.
• Provide medical oversight and interpretation of clinical data as the medical monitor for clinical trials, including those outsourced to CRO...
CytelBangalore
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...
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