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1–2 jobs· newest first

Senior Clinical Research AssociateNew
PSI CRO · Taipei, Taiwan
Competitive salaryHybrid · Full-time · Senior
Senior CRA / Clinical Trial Monitor
Saratoga Medical Center · Remote, US
Remote · Senior

+10K new in the last hour

Senior Clinical Research Associate

PSI CRO · Posted Nov 10, 2026

Taipei, Taiwan, Taiwan
Hybrid
Full-time · Senior
Competitive salary
4–5 years

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Senior CRA to manage the clinical aspects of full-service global projects in Taiwan.

Responsibilities

Training, mentoring and supervising study level responsibilities for Junior CRAs
Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits
Delivering training of investigators, site staff and project teams
Work with complex studies
Perform CRF review, source document verification and query resolution

Requirements

College/University degree in Life Sciences or an equivalent combination of education, training & experience
Nice to have: Inflammatory Bowel Disease
Nice to have: Oncology
Nice to have: Infectious Diseases

Skills

clinical monitoring site management CRF review source document verification query resolution feasibility assessment study set-up processes

Benefits

Development and learning opportunities
Chance to make a real impact in a meaningful industry

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Senior CRA / Clinical Trial Monitor

Saratoga Medical Center · Posted Nov 5, 2026

Remote, United States
Remote
Senior
5+ years

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Senior CRA / Clinical Trial Monitor role focused on NIH- or FDA-regulated clinical research programs.

Compensation

competitive rate and benefit options

Responsibilities

Conducting site initiation, interim monitoring and close-out visits, on-site and remote
Expertise in source document verification, informed consent review, and protocol and GCP compliance assessment
Reviewing adverse event and serious adverse event documentation and reporting
Investigational product accountability, storage and reconciliation
Writing clear monitoring reports, identifying deficiencies, and developing and tracking corrective and preventive actions (CAPA)

Requirements

Bachelor's degree in a life science
nursing
health-related field
Nice to have: clinical research certification (CCRA, CCRP)

Skills

clinical monitoring experience source document verification informed consent review protocol and GCP compliance assessment

adverse event reporting

investigational product accountability

CAPA development

Good Clinical Practice (ICH E6)

21 CFR Parts 11, 50, 54, 56, 312 and 812

human subjects protections training

Benefits

benefit options

See full job description