96 Clinical Data And Biostatistics jobs in Bengaluru.

Bengaluru

• Skills: Data Management, Clinical Trials, Statistical Programming, IT, Biostatistics, Regulatory Affairs, Clinical Research, Medical Writing, Functional Service Provider, Human Resources

Bengaluru

• Skills: biostatistics, clinical trials, data management, statistical planning, design, analysis, reporting, project life cycle, subject matter expert, quality auditing

Bengaluru

• Skills: clinical documents, writing, editing, QC review, clinical study protocols, regulatory guidelines, SOPs, clinical trial, oncology, rare disease
• Experience: 5+ years of experience as a medical writer in the sponsor and/or CRO setting

Bengaluru

• Skills: SAS, programming, clinical trial, statistical analysis, data manipulation, quality control, data listings, report generation, EDC systems, biostatistics
• Experience: 5-8 years
• Type: Full Time

Bengaluru

• Skills: pharmacovigilance, risk management, clinical development, patient safety, safety data, regulatory reports, third-party contracts, training and mentoring, data evaluation, safety expertise
• Experience: 11 to 13 years in Patient Safety (Pharmacovigilance), total of 14 to 16 years of experience.
• Type: Full time

Bengaluru

• Skills: study design, edit specifications, quality delivery, eCRF, EDC build components, Study Authorization Form, Internal Design Review Meeting, database design, LLRR data, Rights and Roles
• Type: Full time

Bengaluru

• Skills: Clinical Programming, Data Analytics, Biostatistics, Data Manipulation, Clinical Safety Review, Visualization, Reporting Solutions, Stakeholder Management, Project Management, CDISC
• Experience: 4+ years of relevant experience in pharmaceutical industry is desired.
• Type: Hybrid

Bengaluru

• Skills: medical review, adverse events, pharmacovigilance, safety data, clinical data, regulatory requirements, safety profiles, signal detection, aggregate reports, GCP
• Experience: Three (3) years experience practicing clinical medicine after award of medical degree.
• Type: Full time

Bengaluru

• Skills: clinical databases, data management, Medidata Rave, programming, scripting, clinical research, CDISC standards, data management systems, communication skills, therapeutic experience

Bengaluru

• Skills: Implementation, Clinical Trials, Lifesciences, SQL, APIs, Integrations, Agile, FDA regulations, Product Lifecycle, Healthcare Software
• Experience: 3-5 years as a Product Manager or 1-2 years as a Product Owner

Bengaluru

• Skills: clinical monitoring, report review, SOP, protocols, projct management, quality improvement, clinical trials, risk assessment, mentoring, regulatory compliance
• Experience: Minimum 3 years experience in clinical monitoring, clinical trial management or equivalent

Bengaluru

• Skills: SAS programming, SDTM, ADaM, clinical trials, data transformation, programming specifications, data analysis, clinical data, data presentations, clinical trial methodologies
• Experience: Minimum 6 years in Pharmaceutical/Biotechnology industry or equivalent IT consulting role

Bengaluru

• Skills: medical affairs, thought leaders, treatment trends, medical education, strategic medical affairs plan, scientific data, patient outcomes, disease trend analysis, pharmaceutical, clinical research
• Experience: Fresh postgraduate or up to 2 years of experience in Field based Medical Affairs

Bengaluru

• Skills: Statistical Programming, SAS, data analysis, clinical trials, biostatistics, programming languages, project management, regulatory guidelines, cross-functional teams, innovation
• Experience: Approximately 6-8 years programming experience with growing responsibility, preferably in a pharmaceutical/clinical trial environment.
• Type: Hybrid

Bengaluru

• Skills: Life Sciences, Solution Architecture, Drug Development, Cloud Platforms, AI/ML, Healthcare, Clinical Trials, Pharmaceutical Research, Compliance, Technical Guidance
• Experience: 5+ years of experience in solution architecture or technical leadership roles within life sciences or health tech industries.

Bengaluru

• Skills: Regulatory Affairs, Data Management, MDRiM, Data Quality, Compliance, MedTech, Medical Device, Process Improvement, Database Management, Cross-functional Environment
• Experience: 3+ years
• Type: Hybrid

Bengaluru

• Skills: regulatory submissions, regulatory documentation, compliance, FDA, EMA, clinical trial, document management, regulatory guidelines, eCTD, submission processes
• Experience: 1-2 years

Bengaluru

• Skills: Data Analysis, SQL, Tableau, Data Visualization, Clinical Data, Healthcare, Data Management, Data Integrity, Regulatory Standards, Data Interpretation
• Experience: 3+ years in a similar role, preferably in clinical or healthcare setting

Bengaluru

• Skills: Tableau dashboards, SQL programming, clinical data management, discrepancy management, data analysis, data visualization, protocol information, quality assurance, data validation, clinical trials

Bengaluru

• Skills: Clinical Data Management, Database Development, Quality Control, Data Management Documentation, Training, Clinical Trial, Medical Coding, CRF Specifications, Database Testing, Regulatory Compliance
• Experience: 5+ years’ Clinical Data Management experience
• Type: Full-time

Bengaluru

• Skills: SAS Programming, Statistical Computing, Clinical Data Standards, SDTM, ADaM, Pharmaceutical Statistics, Clinical Trials, Good Clinical Practices, Technical Specifications, Data Validation
• Type: full_time
• Salary: {'min': None, 'max': None, 'period': '', 'currency': ''}