Clinical Research Associate II (Contract based)

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 :

Make the right call and take your career to a whole new level.  Join the company that focuses on its people and invests in their professional development and success.

Remote Work :

Yes

Employment Type :

Contract