Found Description
Position: Junior Clinical Development. Location: Azuqueca de Henares.
Minimum experience: 3 to 5 years in similar roles.
Responsibilities
- Planning, designing, organizing, supervising the conduct and reporting of clinical trials contracted to Clinical Research Organizations (CROs) to meet timelines and comply with GCP and other applicable requirements.
- Support the design and day‑to‑day management of PK and bioequivalence (BE) trials, and when required, multicenter phase II and III studies.
- Prepare and maintain documents supporting clinical strategy, study rationale, and justifications, and communicate effectively with CRA/CTA and reporting lines.
- Participate in the selection and coordination of CROs and external vendors, ensuring compliance with agreed cost, quality, and time requirements.
- Review study documentation throughout the trial lifecycle (protocol, informed consent form, monitoring reports, study report).
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