Clinical Research Associate 2

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

📋 Description

• Operate within a sponsor-dedicated model for a single client, a leading pharmaceutical company ranked in the top five.

• Oversee activities related to the setup and monitoring of clinical studies.

• Accurately complete study status reports and maintain comprehensive study documentation.

• Execute clinical trial monitoring activities effectively.

• Efficiently manage sponsor-generated queries and take accountability for the cost efficiency of studies.

• Engage in the preparation and review of study documentation and feasibility assessments for new proposals as needed.

• Cultivate and sustain cooperative relationships with key stakeholders, clinical investigators, and site personnel.

• Guarantee patient safety and adherence to ICON procedures, protocols, and regulatory standards.

⛳️ Requirements

• A university degree in medicine, science, or a related field.

• Experience as a Clinical Research Associate.

• Monitoring experience, which includes conducting independent on-site monitoring visits and Site Initiation Visits (SIVs).

• Experience with Site Qualification Visits (SQVs) is preferred but not essential.

• Familiarity with ICH-GCP guidelines.

• Ability to review and assess medical data proficiently.

• Exceptional written and verbal communication skills in English.

• Strong interpersonal skills that enable timely responses to inquiries.

• Willingness to travel as necessary (approximately 60%).

• Must have the legal right to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career pathways.