751 clinical research jobs in India.

... maintenance, and closure - Develop new clinical research sites and expand territory capabilities Requirements - Strong knowledge of ICH-GCP guidelines and clinical trial regulations - Experience in clinical site management and monitoring activities - Proficiency with clinical trial management systems and electronic trial ...

... clinical research capabilities. Required Skills: Accountability, Accountability, Adaptability, Adverse Event Reporting System, Business Activity Monitoring, Clinical Development, Clinical Reporting, Clinical Research, Clinical Research Methods, Clinical Site Management, Clinical Study Management, Clinical Trial Planning, ...

... qualification or equivalent experience. - Substantial startup experience or equivalent experience in clinical research, with demonstrated understanding of clinical trial methodology and terminology. - Knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes. - Experience with Clinical Trial ...

... site and CRA operational issues in coordination with study clinical research manager Requirements - Master's degree in Science, Pharmacology, Pharmacy, or Clinical Research - Expertise in ICH/GCP regulations and Good Documentation Practices - Demonstrated experience managing clinical research teams and CRA personnel - ...

... Adaptability, Career Planning, Clinical Research, Clinical Research Management, Clinical Trial Documentation, Clinical Trial Management, Clinical Trial Planning, Clinical Trials Monitoring, Clinical Trials Operations, Cross-Cultural Awareness, Decision Making, Ethical Standards, Global Coordination, Good Clinical Practice (GCP), ...

... Bachelor’s Degree in Dentistry (BDS) from a recognized institution. Clinical & Professional Experience Minimum 1 to 2 years of post-degree experience in active clinical dental practice. Research Background Demonstrated interest in dental research; prior exposure to clinical trials, basic research, or academic research projects ...

... scientific editorial quality assurance. - Systematic reviews and evidence synthesis. - Clinical practice guideline development. - Clinical trial operations and Good Clinical Practice (GCP). - Research data quality assessment and scientific literature appraisal. Core Skills and Expertise Clinical research, clinical trial design, ...

... scientific editorial quality assurance. - Systematic reviews and evidence synthesis. - Clinical practice guideline development. - Clinical trial operations and Good Clinical Practice (GCP). - Research data quality assessment and scientific literature appraisal. Core Skills and Expertise Clinical research, clinical trial design, ...

IQVIA seeks a Clinical Data Specialist to support clinical data management operations, handling protocol coordination, data review, database testing, and coding tasks. The role may include team leadership responsibilities under supervision within a clinical research organization. Responsibilities - Serve as Data Operations ...

... has delivered 13 million sessions of mental health care, published more than 20 peer-reviewed studies, and delivered unmatched outcomes in terms of access, clinical effectiveness and cost efficiency. Extensive peer-reviewed research confirms Lyra’s transformative care model helps people recover twice as fast and results ...

ICON Strategic Solutions seeks an experienced Clinical Trial Manager to oversee end-to-end clinical trial operations in a sponsor-dedicated model. The role encompasses study start-up, regulatory submissions, site contracting, budget management, and vendor oversight to support global clinical research initiatives. Responsibilities ...

... resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate ...

... science and artificial intelligence, along with advanced data sources such as electronic health records (EHR), to generate RWE capable of supporting complex clinical studies. Some of the largest biopharma companies in the world are Verantos customers. We use a heterogeneous tech stack on AWS with data processing, artificial ...

... coordinating with cross-functional stakeholders to ensure timely clinical trial delivery aligned with R&D goals. Responsibilities - Supervise and coordinate Clinical Trial Managers, Monitors, Associates, and Site Contract Leads to ensure timely execution - Allocate study resources aligned with R&D and local research priorities; ...

... collaboartion with appropriate stakeholders - Identifies unanswered questions and residual risks in the Clinical Evidence and provides input to Post Market Clinical Follow Up activities in collaboration with Clinical Research team to address these questions - Reviews clinical evaluation documentation authored by peers, ...

... Advanced computer applications like Microsoft excel, word, Inbox etc Advanced • Should have Advanced understanding of Drug development lifecycle and Overall Clinical research process Advanced IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences ...

Staff Clinical Evaluation Specialist responsible for developing clinical evidence strategies across product development cycles, preparing regulatory submissions, and conducting systematic literature reviews. Role requires coordination with marketing, regulatory, and research teams to establish device safety and performance ...

Clinical Systems Lead, Bangalore/Chennai, Office based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work ...

Labcorp seeks a Clinical Data Analyst II to manage data discrepancies and reconciliation between clients and internal databases in clinical research. The role involves collaborating with sponsors and CROs, ensuring data quality, and serving as the primary liaison for resolving complex data issues while maintaining regulatory ...

Senior Clinical Data Coordinator role at a global contract research organization, leading data management activities for clinical trials in a sponsor-dedicated model. Responsible for designing data strategies, ensuring regulatory compliance, resolving data issues, and mentoring junior coordinators across multiple Indian ...