Clinical Research Associate II

Job Description

As a Clinical Research Associate at PSI you will be involved in improving patients' lives while enjoying a variety of monitoring tasks and working on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Home-based in Portugal

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
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Be involved in site identification process
• Support regulatory team in preparing documents for study submissions
• Prepare for and participate in audits and inspections

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience.
• At least 2 years of independent on-site monitoring experience in Portugal.
• Experience in Oncology, Hematology is a plus.
• Full working proficiency in Portuguese, English and MS Office applications.
• Ability to plan, multitask and work in a dynamic team environment.
• Communication, collaboration, and problem-solving skills.
• Ability to travel and valid driver’s license.

Additional Information

• PSI is a stable, privately-owned company, organically growing since 1995.
• We have an excellent reputation in the industry, having won the CRO Leadership awards several years in a row.
• Team collaboration is high on our agenda. Our aim is for employees to feel valued and heard in friendly and supportive teams.
• We offer extensive training programs, profound therapeutic area trainings, monitors training program, mentorship programs, interactive soft-skills trainings and more.
• PSI CRAs have an opportunity to work with different Sponsors on a variety of therapeutic areas.

Please provide your CV in English.