Position

Junior Clinical Development

Location

Azuqueca de Henares

Experience

3 to 5 years in similar roles.

Responsibilities

• Plan, design, organize, supervise the conduct and reporting of clinical trials contracted to Clinical Research Organizations (CROs) to ensure studies are completed within planned timelines and comply with GCP and other applicable requirements.
• Focus on pharmacokinetic (PK) and bioequivalence (BE) trials; provide support for multicenter clinical trials and Phase II/III studies as needed.
• Prepare and maintain documents that support the clinical strategy, study rationale, and justifications.
• Communicate effectively with CRAs/CTAs and the reporting line team leader.

Challenge

Support the design and day‑to‑day management of clinical/preclinical trials in compliance with applicable laws, regulations, and guidelines, including ICH, EMA, FDA, and others. ...