Last updated: 2025-05-22

12 Clinical Operations Management jobs in Taipei.

Hiring now: Sr Statistical Programmer @ Parexel, Site Activation Spec Ssur @ Iqvia, Sr Cra @ Psi, Pv Mgr @ Novo Nordi, Cra Ii Sr Cra @ Syneos Hea.Explore more at at kaamvaam.com

šŸ”„ Skills

clinical research (5) clinical trials (4) project management (4) regulatory compliance (4) monitoring (3) site management (3) patient safety (3) statistical programming (2) biostatistics (2) collaboration (2)

šŸ“ Locations

Taipei (12)

Parexel

Skills & Focus: statistical programming, clinical trials, data analysis, Regulatory, biostatistics, collaboration, project management, therapeutic area, sponsor teams, healthcare transformation
About the Company: Parexel is a global biopharmaceutical services company that provides high-quality clinical research and regulatory consulting services.
Type: Full-time

Iqvia

Skills & Focus: Site Activation, clinical research, regulatory documents, project timelines, quality control, negotiating, communication skills, GCP/ICH, drug development, investigative sites
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: 3 years clinical research experience, including 1 year experience in a leadership capacity.
Type: Full time

Parexel

Skills & Focus: clinical research, biostatistics, data management, clinical trials, project leader, regulatory consultants, statistical programming, functional service provider, medical writing, health economics
About the Company: Parexel is a global clinical research organization that specializes in providing services to the pharmaceutical and biotechnology industries. They are dedicate…

Iqvia

Skills & Focus: Clinical Research, Trial Master File, administrative activities, documentation, clinical monitoring, Case Report Forms, Good Clinical Practice, organizing, communication, time 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 industri…
Experience: 3 years administrative support 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 trials, monitoring, site management, study start-up, project stakeholders, communications, study activities, budget negotiations, submissions and approvals, IRB/IEC

Parexel

Skills & Focus: clinical research, monitoring, investigator sites, data integrity, regulatory compliance, problem-solving, relationship building, project management, study protocol, patient safety
About the Company: Parexel is a leading global biopharmaceutical services organization that provides expertise in clinical research and regulatory consulting to help accelerate t…
Experience: Site Management experience or equivalent experience in clinical research
Type: Full-time
Skills & Focus: Clinical Research Associate, site management, monitoring duties, patient safety, study activation, country compliance, site selection, regulatory authority, data management, investigator relationship
About the Company: Parexel is a global biopharmaceutical services company that provides a broad range of integrated services to assist pharmaceutical and biotechnology companies …
Type: Full-time

Iqvia

Skills & Focus: site activation, clinical trials, regulatory strategy, budget management, project management, collaboration, clinical research, technical writing, GCP, ICH guidelines
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: 7 years’ relevant experience in a scientific or clinical environment including demonstrable experience in an international role.
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: medical monitoring, clinical development, protocols, clinical data analysis, safety monitoring, pharmacovigilance, regulatory compliance, GCP guidelines, clinical studies, advisory boards
About the Company: PSI is a leading global clinical research organization (CRO) providing professional services to the pharmaceutical, biotechnology, and medical device industrie…
Type: Full-time

Novo Nordisk

Skills & Focus: pharmacovigilance, team management, safety monitoring, quality assurance, risk management, regulatory compliance, training programs, adverse events, signal detection, communication
About the Company: At Novo Nordisk, we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the …
Experience: Minimum of 5 years in pharmacovigilance or drug safety within the pharmaceutical industry.
Benefits: We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We are happy to d…

Syneos Health

Skills & Focus: clinical research, Good Clinical Practice, monitoring, site management, regulatory compliance, data integrity, clinical data, investigator meetings, audit readiness, patient safety
About the Company: Syneos HealthĀ® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.

Iqvia

Skills & Focus: clinical monitoring, study protocol, good clinical practice, training, site monitoring, study procedures, quality assurance, project management, documentation, regulatory requirements
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: Prior clinical experience preferred. Some organizations may require 2 years of clinical 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.