Last updated: 2025-06-06

19 Clinical Operations Management jobs in Taipei.

Hiring now: Clinical Research Associate Iii @ Parexel, Clinical Associate Development Program T @ Iqvia, Pv Manager @ Novo Nordi, Sr Cra @ Psi. Explore more at at jobswithgpt.com

🔥 Skills

clinical trials (5) project management (5) Clinical Research (4) documentation (3) communication (3) Clinical Trials (2) statistical programming (2) biostatistics (2) collaboration (2) clinical monitoring (2)

📍 Locations

Taipei (11)

Parexel

Clinical Research Associate I/II

Taipei

  • Skills: Clinical Trials, Clinical Research, Biostatistics, Statistical Programming, Data Management, Project Leader, Regulatory Consultants, Statistical Programmers, Emerging Talent, Clinical Operations

IQVIA

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…

Clinical Associate Development Program (Trainee)

Taipei

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

Parexel

Parexel is a global clinical research organization that specializes in providing services to the pharmaceutical and biotechnology industries. They are dedicate…

Functional Service Provider

Taipei

  • Skills: clinical research, biostatistics, data management, clinical trials, project leader, regulatory consultants, statistical programming, functional service provider, medical writing, health economics

Novo Nordisk

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 …

PV Manager

Taipei

  • Skills: pharmacovigilance, team management, safety monitoring, quality assurance, risk management, regulatory compliance, training programs, adverse events, signal detection, communication
  • Experience: Minimum of 5 years in pharmacovigilance or drug safety within the pharmaceutical industry.

PSI

Senior CRA

Taipei

  • Skills: clinical trials, monitoring, project management, study start-up, site management, regulatory, communication, budgets, timelines, informed consent