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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in coordinating clinical trials, managing study documentation, and ensuring compliance with regulations. Proficient in data entry and review within electronic systems, with strong organizational and communication skills.
Highest-signal resume keywords
Clinical Trial CoordinationData Entry and ReviewGood Clinical Practice (ICH-GCP)Organizational SkillsEnglish Language Proficiency (B2 Level)
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 ResearchStudy Documentation ManagementData ManagementQuery ResolutionBiological Sample Management
Soft Skills
Attention to DetailCommunication SkillsTeamwork SkillsProactive AttitudePatient-Centred Approach
Tools & Technologies
Electronic Case Report Forms (eCRF)
Industry Keywords
Healthcare SectorClinical TrialsMonitoring VisitsAuditsInspections
About the role
Key responsibilities & impact- Coordinate the activities of clinical trials
- Manage and maintain study documentation and records
- Enter and review data in the trial’s electronic systems (eCRF)
- Manage and resolve queries
- Provide support during monitoring visits, audits and inspections
- Ensure compliance with applicable procedures and regulations
- Coordinate the dispatch and management of biological samples
- Collaborate with investigators, CRAs, sponsors and other professionals involved in the study
Requirements
What you’ll need- A university degree in Health Sciences, Nursing, Pharmacy, Biology, Medicine or a related discipline
- Previous experience in clinical research or similar roles within the healthcare sector
- Minimum 6 months of experience; work placements count as experience
- English language proficiency at B2 level or above
- Strong organisational skills and the ability to prioritise
- Attention to detail and a focus on quality
- Communication and teamwork skills
- A proactive attitude and a patient-centred approach
- Specific training in clinical research is a plus
- Knowledge of Good Clinical Practice (ICH-GCP) and the regulations applicable to clinical trials is a plus
Benefits
Comp & perks- Be part of a leading international network in clinical research
- Contribute directly to patients’ access to innovative treatments
- Work alongside professionals with extensive experience in clinical research
- Take part in studies across different therapeutic areas and innovative projects
- Enjoy a collaborative, dynamic environment focused on professional development