Last updated: 2025-05-22

15 Clinical Operations Management jobs in Bengaluru.

Hiring now: Sr Clinical Data Associat @ Precision , Clinical Proj Mgr @ Alimentiv2, Proj Leadership @ Parexel, Sr Regulatory Admin Clini @ Precisionm, Proj Mgr @ Endpoint C, Clinical Proj Mgr @ Psi, Clinical Medical Mgr @ Novo Nordi, Clinical Db Designer @ Iqvia, Clinical Database Program @ Eclinical .Explore more at at kaamvaam.com

🔥 Skills

SOPs (4) Clinical Trials (4) data management (3) clinical trial (3) clinical databases (3) project management (3) clinical research (3) clinical trials (3) quality control (2) data entry (2)

📍 Locations

Bengaluru (15)

Precision Medicine Group

Skills & Focus: data management, clinical trial, quality control, data entry, database development, clinical databases, medical coding, project management, SOPs, data review
Experience: 5+ years’ experience

Alimentiv-2

Skills & Focus: clinical research, project management, multidisciplinary team, risk management, project protocols, operational plans, regulatory requirements, project tools, monitoring, accountability

Parexel

Skills & Focus: project plans, SOPs, ICH, GCP, risk management, clinical trials, development, treatments, leadership, biopharma

Precision Medicine Group

Skills & Focus: investigator grants, site budgets, clinical trials, proposal development, financial analysis, Excel proficiency, client communications, team management, budget coordination, operational timelines
About the Company: Precision Medicine Group is an Equal Opportunity Employer committed to providing exceptional services in the context of clinical trials and site budget develop…
Experience: 8 years' experience in site budget and proposal development in the life sciences arena.
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

Parexel

Skills & Focus: Project Leadership, Clinical Trials, Project Plans, Clinical Research, Biostatistics, Statistical Programming, Compliance, SOPs, ICH, GCP
About the Company: Parexel is a leading global biopharmaceutical services organization that helps clients accelerate the development of innovative therapies and provide market ac…
Skills & Focus: Clinical Operations, Project Management, Team Oversight, Resource Management, Client Management, Staff Development, Business Development, Clinical Trials, Performance Monitoring, Quality Assurance
About the Company: Parexel is a global clinical research organization dedicated to providing high-quality clinical trial services. They focus on advancing science and improving t…
Experience: Substantial monitoring/data management experience or equivalent experience in clinical research.
Type: Full-time
Benefits: Flexible Work Arrangement, Career Advancement, Corporate Responsibility.

Precision Medicine Group

Skills & Focus: clinical trial, data management, database development, quality control, clinical databases, data entry, medical coding, SOPs, UAT, clinical research
About the Company: Precision Medicine Group is a healthcare organization that provides data management and support for clinical trials.
Experience: 2+ years’ experience

Precisionmedicinegroup

Skills & Focus: regulatory documents, FDA, EMA, clinical trial, eCTD, submission, regulatory compliance, document management, regulatory guidance, clinical research
Experience: 3 years in document management
Type: Full-time

Parexel

Skills & Focus: Clinical Trials, Clinical Research, Biostatistics, Project Management, Regulatory Compliance, Statistical Programming, Health Economics, Medical Writing, Data Management, CRA
About the Company: Parexel is a leading global biopharmaceutical services organization that collaborates with innovative companies to help develop new therapies for patients.
Type: Full-time

Endpoint Clinical

Skills & Focus: client interface, project management, software development lifecycle, cross-functional dependencies, clinical study protocol, project health, issue resolution, customer service, time management, interpersonal skills
About the Company: Endpoint is an interactive response technology (IRT®) systems and solutions provider that supports the life sciences industry.
Experience: 2-4 years’ experience in a software Project Management role, with a proven ability to understand technical concepts and learn very quickly.
Type: Full-time

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

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.

Eclinical Solutions

Skills & Focus: clinical databases, data management, Medidata Rave, programming languages, ICH/GCP guidelines, EDC standards, data delivery, edit checks, CRFs, data reporting tools
Experience: 2+ years in Pharmaceutical/Biotechnology industry or equivalent preferred