Clinical Research Associate I
PSI CRO
•Onsite
About The Position
As a Clinical Research Associate I 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.
Requirements
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Clinical Research or Medical experience
- Independent on-site monitoring experience in the UK
- PC skills to be able to work with MS Word, Excel and PowerPoint
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
- Valid driver’s license
Responsibilities
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup (if applicable)
- 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
Benefits
- support of a knowledgeable and professional team
- develop a variety of skills
- progressing with the company
- contributing to our full-scale challenging projects
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
