Clinical Research Associate I

Summary

Join our dynamic global company as a Clinical Research Associate and work on the frontline of medical science, contributing to life-changing projects. You will be responsible for communication with stakeholders, ensuring timelines and standards are met. This home-based role requires building relationships with clinical sites and investigators, focusing on subject well-being and data quality. You will conduct monitoring visits, review data, resolve queries, and manage site communication. The role also involves participation in study startup, feasibility research, and regulatory document preparation.

Requirements

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Experience as a Study Coordinator (or similar role) is required
• Experience working on Gastroenterology clinical trials required
• Full working proficiency in English
• 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 and willingness to travel frequently
• 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

Preferred Qualifications

• 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