Clinical Development Analyst

Location:
Brazil (hybrid / remote with on-site visits)

Type:
12-month contract (high possibility of further renewals)

Clinergy Health is a boutique CRO focused on delivering high-quality, highly tailored clinical development solutions for pharmaceutical and biotech companies operating in Brazil and Latin America.

We deliberately work with a selected number strategic projects ranging from phase 1 to RWE to ensure scientific rigor, operational excellence, and close collaboration with our clients.

We are now expanding our team and looking for a Clinical Trials Analyst to support our growing portfolio of clinical development projects.

The Role

This position is ideal for a professional with previous experience in clinical trial monitoring who is looking to expand beyond a traditional CRA role looking into further professional development.

As a Clinical Trials Analyst, you will work closely with the Project Lead, supporting key activities across the entire study lifecycle — from start-up through execution — while maintaining hands-on involvement in on-site monitoring.

This is a
hybrid role
, combining:

• Strategic and analytical project-support activities
• Operational involvement in study start-up and trial conduct
• Selective on-site monitoring, with a more balanced travel model

Key Responsibilities

Study Start-Up & Project Support

• Support clinical trial start-up activities (site selection, feasibility support, essential documents, regulatory and ethics submissions follow-up)
• Assist the Project Lead in planning, tracking, and coordinating study activities
• Support the preparation and maintenance of study plans, trackers, and project documentation
• Contribute to risk identification and mitigation activities during study conduct

Trial Conduct & Management

• Support day-to-day trial execution activities, including site communication and issue follow-up
• Assist with oversight of timelines, deliverables, and study milestones
• Participate in cross-functional interactions with sponsors, vendors, and sites
• Contribute to the preparation of reports, status updates, and study documentation

On-Site Monitoring

• Perform on-site monitoring visits according to the monitoring plan (e.g., initiation, routine, and close-out visits)
• Ensure compliance with protocol, GCP, and applicable regulatory requirements
• Review essential documents, source data, and data quality at site level
• Support sites in addressing findings and corrective actions]

Profile We're Looking For

Required

• Background in Life Sciences (e.g., Pharmacy, Biology, Biomedicine, Nursing, or related fields)
• Previous experience in clinical trials monitoring (CRA or similar role)
• Solid understanding of GCP and clinical trial processes
• Willingness to travel for on-site monitoring
• Strong organizational skills and attention to detail
• Good communication skills in English (written and spoken)

Desirable

• Experience supporting study start-up activities
• Exposure to project management or study coordination activities
• Experience working with international sponsors or CROs

Why Join Clinergy Health?

• Broader role than a traditional CRA position
  , with exposure to strategic and project-level activities;
• Real development opportunity
  in clinical trial management and oversight;
• Balanced travel model
  , avoiding the heavy travel burden typical of monitoring-only roles;
• Close collaboration with highly experienced clinical development professionals;
• High scientific and regulatory standards, with real ownership of your work;
• Highly competitive compensation rates.

Note: this role will initially be a 12-month contract position with the possibility of further renewals and/or beaconing a permanente role.

If you are looking to
grow beyond monitoring
, gain a deeper understanding of how clinical trials are planned and managed, and work in a focused, high-quality CRO environment, we would be happy to hear from you.

Applications: online via LinkedIn advertisement or by sending your resume to