Clinical Research Associate I

This is a fully remote position, open to applicants in United States.

📋 Description

• Engage directly with project stakeholders to facilitate communication.

• Ensure adherence to timelines, targets, and standards in clinical research projects.

• Develop and sustain relationships with clinical sites and investigators.

• Prioritize subjects’ rights, safety, and well-being while ensuring data quality compliance.

• Conduct and document all types of onsite monitoring visits.

• Participate in study startup activities (when applicable).

• Execute CRF reviews, source document verification, and query resolution.

• Oversee site communication effectively.

• Act as a liaison for in-house support services and vendors.

• Coordinate with internal project teams regarding the progress of studies.

• Engage in feasibility research activities.

• Assist the regulatory team in preparing documents for study submissions.

⛳️ Requirements

• Bachelor’s degree in Life Sciences or an equivalent mix of education, training, and experience.

• Previous experience as a Study Coordinator (or in a similar position) is essential.

• Preferred experience in Gastroenterology clinical trials.

• Proficient in English with full working capabilities.

• Proficiency in MS Word, Excel, and PowerPoint.

• Strong planning, multitasking, and teamwork abilities in a dynamic environment.

• Excellent communication, collaboration, and problem-solving skills.

• Willingness and ability to travel frequently.

• Valid driver's license is required.

• Must not require a work visa for current or future employment.

🏝️ Benefits

• Access to professional support from a knowledgeable team.

• Opportunities to develop diverse skills.

• Potential for career advancement within the company.

• Involvement in challenging, full-scale projects.