Clinical Research Associate II (Contract based)

PSI CRO·Lisbon, Lisbon, Portugal

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About the role

PSI seeks a contract-based Clinical Research Associate II in Lisbon, described as home-based freelance but requiring onsite monitoring visits and travel. The role covers study startup, site management, data and quality review, feasibility, and regulatory submission support. Applicants need a Life Sciences degree or equivalent education, training and experience, at least one year of independent onsite monitoring experience in Portugal, Phase II/III monitoring experience, mandatory IBD experience, English and Portuguese proficiency, and MS Office skills.

Key requirements

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• At least 1 year of relevant experience
• Required skills: Independent on-site monitoring experience in Portugal, Experience in all types of monitoring visits in Phase II and/or III, IBD/Inflammatory Bowel Diseases experience, CRF review, Source document verification, Query resolution, Site communication and management, Study startup, Country-level study activity, timeline and schedule supervision, Quality control and compliance monitoring, Feasibility research, Regulatory submission support, MS Office applications, Ability to travel, Planning, multitasking, communication, collaboration and problem-solving
• Required languages: English, Portuguese

Opportunity details

• Workplace: Hybrid
• Employment: Contract, Freelance
• Posted: Sep 9, 2026
• Original advert language: English

Full vacancy

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Employer’s role description

Job title: Clinical Research Associate II (Contract based)

Location: Lisbon, Lisbon, Portugal

Employment type: Contract

Company Description

PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

As a Contract Clinical Research Associate II, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Home-based (freelance)

You will:

Conduct and report all types of onsite monitoring visits
Be involved in study startup
Perform CRF review, source document verification and query resolution
Be responsible for site communication and management
Supervise study activities, timelines, and schedules on the country level
Be a point of contact for in-house support services and vendors
Be involved in quality control, such as compliance monitoring and reports review
Participate in feasibility research
Support regulatory team in preparing documents for study submissions

Qualifications

College/University degree in Life Sciences or an equivalent combination of education, training & experience
A minimum of 1 year of independent on-site monitoring experience in Portugal
Experience in all types of monitoring visits in Phase II and/or III
Experience in IBD/Inflammatory Bowel Diseases is mandatory
Full working proficiency in English and Portuguese
Proficiency in MS Office applications
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Ability to travel

Additional Information

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