Clinical Trials Jobs in Bangalore
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Search Results - Clinical Trials Jobs in Bangalore
iProcess Global Research Inc-Bangalore
and study close-out activities, ensuring adherence to protocols.
Qualifications:
• At least 2-3 years of experience as a Clinical Research Associate, with a general focus on clinical trials. Experience in biospecimen collection is a plus but not mandatory...
iProcess Global Research Inc-Bangalore
and study close-out activities, ensuring adherence to protocols.
Qualifications:
• At least 2-3 years of experience as a Clinical Research Associate, with a general focus on clinical trials. Experience in biospecimen collection is a plus but not mandatory...
George Clinical-Bangalore
We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.
Who are we?
• A leading global clinical...
Fortrea-Bangalore
of the job.
Extensive experience and proven skills in the use of SAS® programs within a clinical trials environment including all processes/practices used with a Statistical Programming environment.
Knowledge in all aspects of clinical trials from initial...
Viatris-Bangalore
of project management and data management skills and monitoring of clinical studies. Knowledge of and understanding of Good Clinical Practice and other associated regulations, guidelines and industry standards for clinical trials is required.
Knowledge...
Merck KGaA Darmstadt Germany-Bangalore
As a Clinical Trial Coordinator you will manage activities within a dedicated Center of Excellence for operational deliverables of Clinical Studies with interactions of multiple cross functional Biopharma functions and CROs Your main responsibilities would...
mncjobsindia.com -
ALP Consulting-Bangalore
Standards) data or NCA/Certara Phoenix datasetsTeal experience - Should cover general modules as well as Clinical (Dealing with clinical trial data reporting), and Hermes (For analyzing MultiAssayExperiment objects).
- Experience of widget development- Good...
Lilly-Bangalore
We’re looking for people who are determined to make life better for people around the world.
Support all programming activities required for the data analysis of the clinical trials and create standard datasets (SDTM) and analysis datasets (ADaM...
Recruise India Consulting Pvt Ltd-Bangalore
neuroscience, oncology, cardiovascular, immunology or endocrine expertise). Experience writing regulatory, clinical trial documents and/or publications Experience in clinical development, clinical trial process or regulatory activities.
Demonstrated project...
Akkodis-Bangalore
Key Skills :
Statistical Programming: Proficient in SAS, R, and other statistical software.
Clinical Trials: Extensive experience in clinical trial design, analysis, and reporting.
Data Management: Data validation, cleaning, and integration...
Fortrea-Bangalore
to successfully perform the key responsibilities of the job.
Extensive experience and proven skills in the use of SAS® programs within a clinical trials environment including all processes/practices used with a Statistical Programming environment.
Knowledge in all...
George Clinical-Bangalore
We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.
Who are we?
• A leading global clinical...
Accenture-Bangalore
research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worldâ...
accenture.com -
GlaxoSmithKline-Bangalore
Site Name Bengaluru Luxor North Tower Posted Date Aug 8 2023 The Statistician Clinical Trial Transparency is responsible for coordinating delivery of transparency documents within each therapy area Oncology Specialty Vaccines through...
mncjobsindia.com -
Phastar-Bangalore
trials; working as part of the study team, taking part in specifying, programming and User Acceptance Testing of eCRFs and edit checks; producing and reviewing sections of the Data Handling Manual. Contributing to clinical coding and processing of third...
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