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Study Coordinator
Humaneva Group. Act as a primary point of contact for patients, colleagues, sponsors, and external partners .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates strong organizational skills and attention to detail in managing clinical trial activities and documentation. Proficient in maintaining compliance with clinical research standards while effectively communicating with patients and team members.
Highest-signal resume keywords
Clinical Trial CoordinationElectronic Database ManagementFluent English CommunicationMicrosoft Office ProficiencyHealthcare Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Research ProceduresStudy Documentation PreparationData EntryInformation ManagementCompliance Maintenance
Soft Skills
Highly OrganizedProactive Team PlayerAttention to DetailReliable and ResponsibleAbility to Manage Multiple Priorities
Tools & Technologies
Digital SystemsClinical Systems
Industry Keywords
Clinical ResearchHealthcareMedical Administration
About the role
Key responsibilities & impact- Act as a primary point of contact for patients, colleagues, sponsors, and external partners
- Coordinate and support clinical trial activities at site level
- Maintain and organize study documentation and site files
- Enter, update, and manage information in electronic databases and clinical systems
- Assist in the preparation and review of study-related documentation
- Translate study-related documents and communications when required
- Support investigators and medical staff in day-to-day study activities
- Ensure tasks are completed accurately and within established timelines
- Contribute to maintaining compliance with clinical research procedures and standards
Requirements
What you’ll need- Fluent in English, both written and spoken
- Comfortable working with Microsoft Office and digital systems
- Highly organized and attentive to detail
- A proactive and positive team player
- Eager to learn and develop new skills
- Reliable, responsible, and committed to delivering high-quality work
- Able to manage multiple priorities and meet deadlines
- Interested in developing a long-term career within the clinical research industry
- Previous experience in healthcare, clinical research, or medical administration is an advantage but not essential
- Able and willing to work from the Plovdiv site on a full-time basis
- Applicants should submit a CV together with a recent photo
Benefits
Comp & perks- Competitive salary package
- Performance-based bonus opportunities
- Meal vouchers
- Additional health insurance
- Comprehensive onboarding and training
- Professional development and continuous learning opportunities
- Long-term career growth within Pratia and Humaneva Group
- Exposure to international clinical research projects
- Supportive team environment and collaborative culture
- The opportunity to contribute to research that helps improve patients' lives