Clinical Data Reviewer

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 research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years of...

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 research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years of...

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 research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years of...

Job Overview Provide management and service delivery excellence of (Clinical Event Validation and Adjudication) CEVA, OGM (Oversight Group Management) projects, as assigned by CEVA Management, covering single or multiple CEVA-OGM functions, with supervision from project oversight. Provide administrative coordination for Oversight Groups (Data Monitoring...

Job Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical...

Job Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative medical...

Job Title : Clinical Research Associate (CRA) Company : MS Clinical Research Pvt Ltd About Us : MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative...

Associate Medical Reviewer **Category**:Clinical Development**Location**:Bangalore, Karnataka, IN**Department** - Centralised Monitoring Unit (CMU) - Bangalore- **The Position**: (Note: This is not a role within Pharmacovigilance)- - Responsible for contribution to or participation in trial planning activities related to medical review. - Responsible for...

**Labcorp Drug Development**: As a leading contract research organization (CRO), Labcorp Drug Development provides comprehensive drug development solutions for a range of industries. Our services cover the preclinical, clinical and post-market phases of drug development, the product life cycles for medical device and diagnostics and development services...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

**Brief Position Description**: The Clinical Data Programmer SAS is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating reports,...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

5 years of experience working with Veeva Vault Clinical trial management systems in the pharmaceutical or biotech industry.Lead the implementation and configuration of Veeva Vault Clinical applications to meet business requirements and industry standards.Customize Veeva Vault functionality, including study setup, electronic trial master file (eTMF)...

5 years of experience working with Veeva Vault Clinical trial management systems in the pharmaceutical or biotech industry. Lead the implementation and configuration of Veeva Vault Clinical applications to meet business requirements and industry standards. Customize Veeva Vault functionality, including study setup, electronic trial master file (eTMF)...

Associate Clinical Data Programmer **Category**:Data & AI**Location**:Bangalore, Karnataka, IN**Department**:Data Systems & Automation, Bangalore Global Development- **About the department** - Data Systems & Automation, Bangalore Global Development GBS is one of the most competent and diverse team of professionals who are mainly responsible for providing...

**Job description** **Job Description**: GNM / BSc. with 0 - 3 years of experience. Salary Commensurate with Qualification & Experience. **Role: Clinical Review Nurse** **Industry Type: Medical Services / Hospital** **Department: Healthcare & Life Sciences** **Employment Type: Full Time, Permanent** **Role Category: Nursing** Education **UG: Any...

**About the role**: The Clinical Data Programmer SAS III (must be SAS Certified) is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of facilitating clinical data inspection and quality control, as well as operational performance control of clinical sites by creating...

**Job Title: Clinical Programmer** **Career Level - C** **Skills required - **SAS, SQL, PowerBI, Python, MicroStrategy **Introduction to Role**: Are you ready to take a crucial inter-disciplinary approach to save patients' lives? As a Clinical Programmer, you will be primarily responsible for providing support to activities related to programming,...

Key Responsibilities in this position will be to perform Medical Review of all trial subjects of all assigned clinical trials within drug development portfolio across therapy areas & to ensure high quality consistent medical data. Medical Review is performed for all trial subjects to ensure patient safety and adherence to protocols, Good Clinical...

5 years of experience working with Veeva Vault Clinical trial management systems in the pharmaceutical or biotech industry.Lead the implementation and configuration of Veeva Vault Clinical applications to meet business requirements and industry standards.Customize Veeva Vault functionality, including study setup, electronic trial master file (eTMF)...