Clinical Trial Coordinator I

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

📋 Description

• Coordinates, supervises, and finalizes activities related to assigned trials.

• Conducts reviews of department, internal, country, and investigator files as designated.

• Ensures that assigned tasks are completed punctually, within budget, and to a high-quality standard.

• Actively communicates any potential risks to project leaders.

• Provides support for systems and ensures that system databases are consistently up-to-date.

• Carries out administrative responsibilities for assigned trials.

• Analyzes and reconciles study metrics and findings reports.

• Assists in the coordination, compilation, and distribution of Investigator Site File materials to the respective sites.

• May aid in scheduling client and/or internal meetings.

• Collaborates directly with sites to gather documents necessary for site selection.

• Supports the evaluation of survey data to confirm that responses are logical, complete, and reflective of the questions posed.

⛳️ Requirements

• High school diploma or equivalent qualification.

• Bachelor's degree is preferred.

• Prior experience that equips the candidate with the knowledge, skills, and abilities necessary for the role (approximately 0 to 1 year).

• Capability to work effectively in a team or independently.

• Strong organizational skills and a keen attention to detail.

• Proficient English language and grammar skills, along with necessary local language proficiency.

• Competent computer skills, with proficiency in MS Office (Word, Excel, and PowerPoint).

• Ability to successfully complete the organization's clinical training program.

🏝️ Benefits

• Opportunities for professional development.

• Flexible working hours.

• Paid time off.