Clinical Research Associate

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.

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
• Participate in feasibility research
• Support regulatory team in preparing documents for study submissions
• Support and participate in audits and inspections

Qualifications :

• College/University degree in Life Sciences or an equivalent combination of education training & experience
• At least 1 year of independent on-site monitoring experience
• Experience in all types of monitoring visits
• Full working proficiency in English and Serbian
• 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 across the region
• Valid drivers license

Additional Information :

What We Offer:

• Stability long-term cooperation
• Permanent contract full-time job
• Remote work setting
• Car allowance laptop and mobile phone
• Career development 
• Unique combination of team collaboration and independent work
• Friendly and supportive colleagues
• Onboarding courses about clinical research industry
• Mentoring and on-the job training
• Comfortable office and team support in Banja Luka

This is a great opportunity for you to further develop your skills widen your therapeutic area experience and become an expert in clinical research.

Remote Work :

Yes

Employment Type :

Full-time