10 Clinical Operations Management jobs in Taipei.

Hiring now: Functional Service Provid @ Parexel, Site Activation Spec Ssur @ Iqvia, Pv Mgr @ Novo Nordi, Clinical Research Associa @ Syneos Hea.Explore more at jobswithgpt.com.

šŸ”„ Skills

clinical research (4) Clinical Research (4) clinical trials (3) project management (3) Good Clinical Practice (3) communication (3) biostatistics (2) statistical programming (2) Clinical Trials (2) Data Management (2)

šŸ“ Locations

Taipei (10)

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…
Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Clinical Research, Data Management, Biostatistics, Statistical Programming, Regulatory Consultants, Project Leaders, Health Economics
Type: Full-time
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
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.

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

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.
Skills & Focus: monitoring, site management, Clinical Research, Good Clinical Practice, International Conference on Harmonization, protocol, recruitment, documentation, regulatory requirements, 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: Some organizations require completion of CRA training program or prior monitoring 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.

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, Monitoring, Site Management, Clinical Trials, Regulatory Compliance, Good Clinical Practice, Patient Safety, Data Management, Site Qualification, Sponsor Liaison
About the Company: Syneos Health is a leading integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affa…
Experience: 2 years of clinical monitoring experience
Type: Full-time