Clinical Research Associate

Location: Amadora, Portugal; hybrid role

Company

hirify.global develops innovative medicines and solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

• Build partnerships with investigators and site staff to align study objectives, protocols, patient treatment principles, and regulatory expectations.
• Conduct site qualification, initiation, routine on-site and remote monitoring, and close-out visits for Phase I–IV clinical studies.
• Train site personnel on protocols, study procedures, safety reporting, and regulatory requirements.
• Oversee site activities, identify risks and compliance issues, and support corrective and preventive action plans.
• Ensure timely, high-quality site data and safety-event reporting while protecting study participants.
• Support investigator and site selection, patient recruitment and retention, documentation, payments, agreements, and inspection readiness.

Requirements

• Bachelor’s degree or equivalent in Medicine, Nursing, Pharmacy, Life Sciences, or a related health or scientific discipline.
• At least one year of experience in clinical research monitoring.
• Strong planning, organizational, communication, and interpersonal skills.
• Analytical and problem-solving skills, including the ability to identify site issues and support corrective actions.
• Commitment to quality, compliance, patient safety, ethical conduct, and timely delivery.

Culture & Benefits

• Collaborative, patient-focused clinical operations environment.
• Opportunities to develop expertise across a wide range of clinical research activities.
• Work culture emphasizing teamwork, informed decision-making, accountability, constructive feedback, and adaptability.
• Equal opportunity employer committed to integrity, innovation, and community service.