Clinical Research Physician

About the role

Translational Research in Oncology (TRIO) is seeking a Clinical Research Physician to join its Medical Monitoring Unit. This full‑time position can be performed remotely or in a hybrid model from Uruguay, supporting global oncology clinical trials.

Key responsibilities

• Act as Medical Monitor, conducting 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, 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 scientific questions from internal and external stakeholders.
• Collaborate with Medical Writing and Training units to write or review trial‑specific medical documents (protocols, DSURs, CSRs).
• Conduct medical training on selected trial‑specific or general topics.

Required profile

• Medical Doctor degree.
• Excellent 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).
• Strong teamwork and communication abilities.
• Fluent English; Spanish knowledge is a plus.
• Legal authorization to work in Uruguay.

Required skills

• MS Office (Word, Excel, PowerPoint)

What we offer

• Professional growth opportunities.
• 20 paid vacation days plus paid December holiday closure.
• Flexible working hours and hybrid work arrangement.
• Home office allowance, mobile phone stipend, and internet/transport allowance.
• Premium health insurance for employee and family.
• Employee recognition and referral bonus programs.