This is a fully remote position, open to applicants in Bulgaria, +3 more countries.

📋 Description

• Ensure the quality of data submitted by study sites and guarantee timely data submission.

• Provide appropriate reporting and follow-up on all safety events reported by site personnel.

• Ensure completeness and compile documentation for regulatory and ethical submissions, including IRB approvals, informed consent, and lab certifications.

• Supply relevant updates for site-related documentation to be filed in the Trial Master File (TMF).

• Conduct feasibility studies and site identification activities for potential sites as requested.

• Collaborate with colleagues across different therapeutic areas and contribute to clinical research studies.

⛳️ Requirements

• Exceptional interpersonal, oral, and written communication skills.

• Ability to effectively contribute to a remote team.

• Strong customer orientation and ability to interact professionally with sponsor contacts.

• Proficiency in Microsoft Office, CTMS, and EDC Systems.

• A four-year college degree with a major concentration in life sciences is preferred but not mandatory.

• A two-year college degree or equivalent education and training, along with one year of experience in clinical research or other relevant fields.

• Proficiency in English, Bulgarian, and one additional language: German, French, Italian, or Spanish.

🏝️ Benefits

• Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other classes protected by applicable law.