You will perform centralized monitoring to detect potential signals and trends in clinical trial data.
This role supports the RBQM system and ensures data quality and regulatory compliance.

Key Responsibilities:

Conduct periodic reviews of KRIs and assess site performance for potential issues.
Evaluate study site practices and maintain documentation for centralized monitoring.
Attend study kick-off meetings and recurring project meetings as needed.

Qualifications:

BA/BS in Life Sciences or equivalent, with at least 1 year of clinical research experience.
Understanding of Risk Based Quality Management and ICH-GCP principles.
Strong analytical, communication, and organizational skills.

Why Join Us:

Be part of a passionate team advancing treatments for rare disease and oncology.
Enjoy a collaborative global environment with flexibility and trust.
Your work directly impacts patients who cannot wait.

Ergomed

Ergomed is a specialist clinical research organization focused on rare disease and oncology trials, partnering with small to midsize biotech companies to move therapies through early phase development. With a collaborative international team across North America, South America, Europe, Asia and Australia, we value teamwork, flexibility, and work-life balance, fostering a culture where employees take ownership and grow their careers.

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