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Clinical Project Leader

Trabajo disponible en: 08001, Barcelona, Cataluna, España
Empresa: Discover International
Tiempo completo posición
Publicado en 2026-01-28
Especializaciones laborales:
  • Servicios Médicos
  • Farmacéutico
Rango Salarial o Referencia de la Industria: 70000 - 90000 EUR Anual EUR 70000.00 90000.00 YEAR
Descripción del trabajo
Principal Executive Search Consultant - Medical & Clinical
Clinical Project Manager – Phase I PK/PD & Bioequivalence Studies (Generics)

Location:

Spain

Employment Type:

Full-time, Permanent

About Us
I'm working with a forward thinking pharmaceuticals who are known contributors within the Generics field who are specializing in early-phase clinical development and bioequivalence studies for generic pharmaceuticals. They are committed to the CNS area.

About the Role
We are seeking an experienced  Clinical Project Manager (CPM)  to lead and oversee  Phase I pharmacokinetic (PK/PD), pharmacodynamic (PD), and bioequivalence (BE)  clinical trials. This is a hands-on project management role where you’ll coordinate cross-functional teams, ensure regulatory and GCP compliance, and drive successful delivery of complex early-phase studies.

Key Responsibilities

Lead the planning, execution, and close-out of Phase I PK/PD and BE clinical studies.

Manage study timelines, budgets, and deliverables to ensure projects are completed on time and within scope.

Serve as the primary point of contact for sponsors, clinical sites, and internal teams.

Oversee protocol development, CRF design, and operational planning for bioequivalence studies.

Ensure adherence to ICH-GCP, regulatory guidelines (FDA, EMA, MHRA, etc.), and company SOPs.

Monitor project performance metrics and proactively address risks and deviations.

Collaborate with bioanalytical, data management, and biostatistics teams to ensure seamless data flow and reporting.

Support audits, inspections, and quality assurance activities.

Requirements

Bachelor’s degree (or higher) in Life Sciences, Pharmacy, or related field.

3–5+ years of experience managing Phase I clinical trials, ideally within a Pharmaceuticals, Biotech or CRO or generic drug development environment.

Proven track record in PK/PD and bioequivalence studies.

Strong knowledge of GCP, ICH, and regional regulatory requirements.

Excellent organizational, communication, and leadership skills.

Ability to manage multiple studies simultaneously in a fast-paced setting.

Seniority Level
Mid-Senior level

Employment Type

Full-time

Job Function
Science

Industries
Pharmaceutical Manufacturing and Biotechnology Research

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