Empleos de Fortrea en España

We are seeking a CRA with solid monitoring experience. If you are eager to make an impact, this is your chance. · ...

The Clinical Research Associate II will conduct site management for clinical studies in accordance with Fortrea's Standard Operating Procedures and ICH GCP Guidelines. · ...

We are seeking an experienced Senior Regulatory Medical Writer to lead authoring and development of high complexity clinical regulatory documents that are critical to the strategic projects of our partner. We will trust you to spearhead the entire process, from initial planning a ...

Site management for clinical studies is conducted in accordance with Fortrea's Standard Operating Procedures, ICH GCP Guidelines, applicable project plans, and sponsor requirements. · ...

+Job summary · We're now hiring a Study Start-Up Lead to join a sponsor‑dedicated team and drive the successful planning and activation of clinical trials. · +Partner closely with Clinical Operations to improve study start-up metrics and implement optimized processes. · ...

We're now hiring a Study Start-Up Lead to join a sponsor-dedicated team and drive the successful planning and activation of clinical trials. At Fortrea, we believe in improving lives through the power of science, collaboration, and innovation.Why join Fortrea? · Work in a collabo ...

We are seeking a Sponsor-Dedicated CRA II with solid monitoring experience. · Monitor clinical trial sites to ensure compliance with protocols, GCP, and regulatory requirements. · Build strong relationships with investigators and site staff. · ...

Clinical Research Associate II conducts site management for clinical studies according to Fortrea's Standard Operating Procedures and ICH GCP Guidelines. · ...