Conduct and report all types of onsite monitoring visits.
Perform CRF review, source document verification, and query resolution.
Support study startup, site communication, and audits.
PSI is a leading CRO with 30+ years in the industry, offering stability and innovation. We focus on quality and on-time services across therapeutic indications, with friendly and supportive colleagues.
Work on the frontline of communication with project stakeholders, ensuring timelines, targets, and standards.
Build and maintain relationships with clinical sites and investigators, focusing on subjects' rights, safety, and well-being.
Conduct and report all types of onsite monitoring visits, including CRF reviews and source document verification.
PSI is a leading Contract Research Organisation with 30 years in the industry, offering a balance between stability and innovation. They focus on delivering quality and on-time services across a variety of therapeutic indications.
Conduct on-site or remote monitoring visits to ensure site adequacy for clinical trials.
Train investigational site staff and support regulatory submissions as needed.
Mentor junior staff and perform co-monitoring visits to assess performance.
Ergomed Group provides clinical research, pharmacovigilance, and consulting services to biopharmaceutical companies, focusing on oncology and rare diseases. With a global team, they emphasize collaboration, kindness, and professional growth in a values-driven culture.