Clinical Trials Associate

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

📋 Description

• Coordinate and monitor system access for members of the project team, which includes Project Managers, Lead CRAs, and CRAs.

• Ensure document maintenance and quality audits are conducted to keep the most up-to-date revisions available on project portals.

• Assist the project team in preparing and sending out clinical trial documentation, such as Investigator Site Files.

• Manage document version control and quality assurance, and submit all documentation to the trial master file.

• Track and maintain project-related data, including the site medical question-and-answer log.

• Provide administrative and project-tracking assistance to the clinical project team.

• Ensure that assigned project tasks are completed accurately and within the designated timeframes.

⛳️ Requirements

• Proficient in both written and spoken English.

• Fluent in the language spoken in the country of employment.

• Capable of managing multiple tasks while exercising independent judgment.

• Strong attention to detail with a commitment to quality work.

• Excellent organizational skills and adept at problem-solving.

• Proficient in MS Office applications, including Outlook, Word, Excel, and PowerPoint.

• Possession of a degree-level qualification or equivalent professional experience.

• A minimum of one year of experience in a relevant role.

• Demonstrated skill sets and performance levels equivalent to the aforementioned requirements.

🏝️ Benefits

• A diverse and inclusive work environment.

• Supportive and collaborative teams.

• Accessible and hands-on leadership.

• Equal employment opportunities for all.

• Exceptional employee experiences.

• Opportunities for success for professionals from various backgrounds and experiences.