21 Clinical Operations Management jobs in Bengaluru.

Hiring now: Medical Writer Ii @ Parexel, Associate Medical Writer @ Novo Nordi, Clinical Research Promoti @ Milestone , Centralized Visit Report @ Precision , Local Study Associate Dir @ Astrazenec, Clinical Process Associat @ Iqvia, Clinical Proj Mgr @ Psi.Explore more at jobswithgpt.com.

🔥 Skills

clinical research (4) Clinical Trials (4) clinical trials (4) collaboration (3) Good Clinical Practice (3) clinical monitoring (3) regulatory compliance (3) compliance (3) project management (3) pharmacovigilance (2)

📍 Locations

Bengaluru (21)

Parexel

Skills & Focus: clinical research, regulatory agencies, writing skills, aggregate reports, Clinical Study Reports, pharmacovigilance, signal detection, narrative writing, health authority, data analysis
About the Company: A global biopharmaceutical services organization that provides a range of clinical research, regulatory consulting, and market access services.
Type: Full-time
Skills & Focus: Clinical Research, FSP, Remote, CRA, Biostatisticians, Clinical Trials, Project Leaders, Data Managers, Regulatory Consultants, Statistical Programmers
Skills & Focus: Statistical Programming, Clinical Trials, SAS, Project Management, Quality Control, Data Analysis, Regulatory Compliance, Statistical Analysis Plans, Clinical Data, Team Collaboration
Benefits: Flexible work arrangements, inclusive environment, opportunities for career growth.

Novo Nordisk

Skills & Focus: medical writing, study protocol, clinical document, literature searches, systematic literature searches, collaborative, regulatory requirements, healthcare industry, audit-preparedness, cross-functional collaboration
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases.
Experience: 2+ years of experience in medical writing
Type: Full-time

Milestone One

Skills & Focus: clinical research, healthcare professionals, clinical trial support, gastroenterologists, pharmacists, hospital administrators, Principal Investigators, contract negotiations, collaboration, medical institutions
About the Company: A leading service provider for clinical trial support and related services.
Type: Full-time

Novo Nordisk

Skills & Focus: Clinical Trial, Medical Review, Patient Safety, Protocol Adherence, Good Clinical Practice, ICH Guidelines, Compliance, Data Management, Risk Management, Training
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy …
Experience: 3-5 years of relevant experience in Clinical Drug Development

Precision Medicine Group

Skills & Focus: 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

Astrazeneca

Skills & Focus: clinical trials, study team, compliance, data delivery, stakeholder management, risk management, monitoring, site selection, regulatory submissions, patient recruitment
About the Company: AstraZeneca is a global biopharmaceutical company that focuses on innovative medicines.
Type: Full time
Skills & Focus: regulatory affairs, product licenses, submission plan, dossier compilation, Indian regulations, regulatory compliance, clinical trials, regulatory strategies, documentation, collaboration
About the Company: AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescriptio…
Experience: 3-6 yrs Experience in India Regulatory function
Type: Full time

Precision Medicine Group

Skills & Focus: 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

Iqvia

Skills & Focus: clinical research, project management, data analysis, regulatory compliance, communication, quality assurance, documentation, collaboration, administrative support, vendor coordination
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: minimum 2 years relevant experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Psi

Skills & Focus: clinical project management, study milestones, key performance indicators, study status review, project planning documents, site selection, budget negotiations, monitoring standards, audit preparation, team compliance
About the Company: A global contract research organization focused on advancing the clinical development of new therapies.
Experience: 5+ years in clinical project management
Type: Full-time

Precision Medicine Group

Skills & Focus: clinical monitoring, monitoring visit reports, protocols, SOPs, compliance, action items, safety, study performance, ICH GCP, training
About the Company: Precision Medicine Group is an Equal Opportunity Employer.
Experience: Minimum 3 years experience in clinical monitoring, clinical trial management or equivalent
Skills & Focus: feasibility analysis, pre-award projects, clinical protocols, study assumptions, site identification, enrollment modeling, patient advocacy, analytical thinking, team collaboration, ICH-GCP
About the Company: Precision Medicine Group is a scientifically driven, engaged partner for biotech and pharma clients, providing innovative solutions to complex challenges in cl…
Experience: A minimum of 5 years of related experience

Novo Nordisk

Skills & Focus: Clinical Trials, CVD, CKD, NASH, Research, Medical Guidance, Training, Communication, Stakeholder Engagement, Healthcare Research
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases, focusing on diabetes and expan…
Experience: 2+ years of clinical or pharmaceutical industry experience

Iqvia

Skills & Focus: study design, edit specifications, quality delivery, eCRF, EDC build components, Study Authorization Form, Internal Design Review Meeting, database design, LLRR data, Rights and Roles
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Skills & Focus: study build, eCRF, specifications, system configurations, project financials, database design, process improvements, data management, training documentation, risk communication
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 2-4 years of relevant core Technical designer experience and total experience being 7+ years.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Astrazeneca

Skills & Focus: clinical research, global clinical operations, clinical monitoring, team leadership, pharmaceutical, project management, Good Clinical Practice, clinical study processes, talent development, interpersonal skills
About the Company: AstraZeneca is a global biopharmaceutical company focused on delivering life-changing medicines. After 45 years in India, the company continues to invest in af…
Experience: A minimum of 8 years in global clinical operations within a multinational pharmaceutical company or Contract Research Organization (CRO). Experience must include direct clinical site monitoring for global phase 2/3 studies.
Type: Full time

Novo Nordisk

Skills & Focus: medical review, clinical trial data, Good Clinical Practice, protocol adherence, patient safety, compliance, data management, risk-based monitoring, medical terminology, analytical skills
About the Company: Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy …
Experience: 3-5 years of relevant experience in Clinical Drug Development
Type: Full-time

Iqvia

Skills & Focus: pharmacovigilance, adverse events, clinical trials, medical safety, regulatory requirements, data safety, project management, staff management, medical review, risk management
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Three (3) years of clinical practice experience with two (2) additional years in the pharmaceutical or associated industry.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.