Senior Clinical Research Associate

PSI CRO; West Coast; Hybrid; AUD 80,000 - 100,000; Full time

Job summary

A leading clinical research organization is seeking an experienced professional for on-site monitoring in clinical trials. This role involves ensuring compliance with study protocols, managing site activities, and performing documentation reviews. Ideal candidates have a university degree in Life Sciences and at least 5 years of monitoring experience, particularly in Oncology or Hemophilia trials. The position offers the flexibility to work remotely or from the office.

Benefits

Opportunity for career advancement

Flexible work environment

Collaborative work culture

Qualifications

• 5+ years of independent on-site monitoring experience in clinical trials.
• Experience with Oncology and/or Hemophilia trials.
• Full working proficiency in English.

Responsibilities

• Conduct onsite monitoring visits to ensure compliance with study protocols.
• Manage site communication and oversee study activities.
• Perform CRF review and source document verification.

Skills

On-site monitoring experience

Strong communication skills

Problem-solving skills

Collaboration skills

Education

College/University degree in Life Sciences

Tools

MS Office applications

Job description

Employer Industry: Clinical Research

Why consider this job opportunity:

• Opportunity for career advancement and growth within a rapidly expanding organization
• Work remotely or from the office, providing flexibility in your work environment
• Engage in meaningful work that impacts the lives of patients through clinical trials
• Competitive salary and benefits package
• Collaborative work culture focused on employee well-being and development

What to Expect (Job Responsibilities):

• Conduct and report all types of onsite monitoring visits to ensure compliance with study protocols
• Manage site communication and oversee study activities, timelines, and schedules at the country level
• Perform CRF review, source document verification, and query resolution
• Participate in feasibility research and support the regulatory team with study submissions
• Supervise quality control efforts, including compliance monitoring and report reviews

What is Required (Qualifications):

• College/University degree in Life Sciences or equivalent combination of education, training, and experience
• Minimum of 5 years of independent on-site monitoring experience in the USA
• Experience in all types of monitoring visits in Phase II and/or III clinical trials
• Proven background in monitoring Oncology and/or Hemophilia trials
• Full working proficiency in English and proficiency in MS Office applications

How to Stand Out (Preferred Qualifications):

• Experience as a Lead/Senior Monitor in clinical research projects
• Strong communication, collaboration, and problem-solving skills
• Ability to plan and multitask effectively in a dynamic team environment
• Valid driver’s license (if applicable)

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