Job Overview
Job description
- Location:
- Lithuania
- Work arrangement:
- On-site
Role Summary
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.
Remote opportunity in Lithuania
Requirements
You will
- Conduct and report all types of onsite monitoring visits
- 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
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent monitoring experience in Lithuania, preferably on contractor/freelance position
- Full working proficiency in English and Lithuanian
- Knowlegde of Latvian is a plus
- 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
- Valid driver's license
Benefits
- Flexible working conditions
- Extensive training and friendly team
- Opportunities for personal and professional growth
- Competitive salary starting at 45 euro per hour. The precise salary depends on the specific qualifications and experience, and will be agreed upon on an individual basis.
- If you feel it is time to make your skills and knowledge visible within a company with true focus on its people, then PSI CRO is the right choice for you.
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
About the Company
Why Join PSI?
At PSI, we believe exceptional people deserve an exceptional workplace.
When you join PSI, you'll benefit from
A stable, privately held CRO that has never undergone a merger or acquisition and has never experienced company-wide layoffs.
A unique leadership-focused CRA role with minimal travel and little to no routine site assignments.
Opportunities to mentor other CRAs and expand your leadership skills.
A collaborative, people-first culture where employees are genuinely supported.
Career development opportunities across a growing global organization.
The chance to contribute to innovative clinical research that improves patients' lives.
We are the company that cares - for our staff, our clients, our partners, and the quality of the work we do.
Founded in 1995, PSI CRO is a privately owned, global Contract Research Organization with more than 3,000 employees dedicated to advancing medical science and bringing new therapies to patients worldwide.
In an industry shaped by mergers, acquisitions, and restructures, PSI stands apart. We have remained privately held, have never undergone a merger or acquisition, and have never experienced company-wide layoffs. Our long-term stability allows us to invest in our people, foster meaningful careers, and build lasting partnerships with our clients.
If you're looking for a collaborative organization where you can continue to grow while making a meaningful impact, PSI is the right place for you.
- Role:
- Contract Clinical Research Associate
- Job Type:
- Contractor