Data Entry, Study Coordinator

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

📋 Description

• Oversee the execution of clinical trial activities

• Organize and uphold study documentation and records

• Input and assess data within the trial's electronic systems (eCRF)

• Address and resolve inquiries

• Offer assistance during monitoring visits, audits, and inspections

• Ensure adherence to relevant procedures and regulations

• Coordinate the shipment and management of biological samples

• Work collaboratively with investigators, CRAs, sponsors, and other professionals involved in the study

⛳️ Requirements

• A university degree in Health Sciences, Nursing, Pharmacy, Biology, Medicine, or a related field

• Prior experience in clinical research or comparable roles within the healthcare industry

• At least 6 months of experience; internships are considered as experience

• Proficiency in the English language at B2 level or higher

• Excellent organizational abilities and capability to prioritize tasks

• Strong attention to detail and commitment to quality

• Effective communication and teamwork skills

• A proactive mindset with a patient-centered approach

• Specialized training in clinical research is advantageous

• Familiarity with Good Clinical Practice (ICH-GCP) and regulations relevant to clinical trials is a plus

🏝️ Benefits

• Become part of a leading global network in clinical research

• Play a direct role in enhancing patients' access to innovative treatments

• Collaborate with professionals possessing extensive experience in clinical research

• Participate in studies across various therapeutic areas and innovative projects

• Experience a collaborative and dynamic environment that emphasizes professional growth