Clinical Research Physician

About the role

TRIO is seeking a qualified Clinical Research Physician to join its Medical Monitoring Unit. This full‑time, home‑based position in Spain supports the safety and scientific integrity of oncology clinical trials.

Key responsibilities

• Act as Medical Monitor, performing comprehensive medical monitoring activities.
• Respond to medical inquiries from investigational sites and trial teams.
• Review patient eligibility, protocol deviations, and patient safety data.
• Assess Serious Adverse Events (SAEs), including coding, causality, and expectedness, and draft company comments.
• Prepare scientific slides and present protocol information at Investigator Meetings, Scientific Committee meetings, Safety Review Committee meetings, and Site Initiation Visits.
• Serve as the primary clinical point of contact for internal and external stakeholders (IRBs, sites, sponsor medical teams, trial teams).
• Collaborate with Medical Writing and Training units to write or review trial‑specific documents (protocols, DSURs, CSRs).
• Conduct medical training on selected trial‑specific or general topics.

Required profile

• Medical Doctor degree.
• Strong knowledge of oncology and oncology clinical trials.
• Minimum 1 year experience in medical monitoring for oncology trials.
• Current knowledge of ICH GCP guidelines.
• Advanced proficiency in MS Office (Word, Excel, PowerPoint).
• Excellent teamwork and communication abilities.
• Fluent English; Spanish language knowledge is a plus.
• Legally authorized to work in Spain.

Required skills

• MS Office (Word, Excel, PowerPoint)

What we offer

• Annual competitive review with professional growth opportunities.
• Paid vacation days and flexible working hours.
• Monthly internet allowance for remote work.
• One‑time home office allowance.
• Employee recognition and referral bonus programs.