Data Entry, Study Coordinator

• 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

• 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

• 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