Clinical Research Associate I

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.

You will:

• 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

Qualifications :

• 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 drivers license 

Additional Information :

Become a full-fledged clinical research professional with the support of a knowledgeable and professional team.  You will develop a variety of skills while progressing with the company and contributing to our full-scale challenging projects.

Remote Work :

Yes

Employment Type :

Full-time