Clinical Trial Manager (Biotech)

Barcelona Permanente EUR40.000 - EUR45.000 por año Ver descripción del puesto
The Clinical Trial Manager (CTM) is responsible for the operational management and oversight of clinical trials from study start-up through close-out. The CTM ensures that trials are conducted in accordance with ICH-GCP guidelines, regulatory requirements, and company SOPs, while meeting timelines and budget expectations

Added 23/04/2026

  • Oncology & SNC
  • Development of epigenetics-based therapeutics.

¿Dónde vas a trabajar?

Multinational Biotech Company

Descripción

  • Primary point of contact for Clinical Operations aspects of designated projects: act as main contact for CROs and other clinical providers and for internal clients
  • Responsible for planning, scheduling and implementing the Clinical Operations aspects of projects in collaboration with CRO
  • Responsible for risk mitigation strategies, associated action plan and issue resolution in collaboration with CRO
  • Responsible for oversight the project development to ensure deliverable on time and within budget
  • Manage the relationship with CRO and clinical providers, identify needs and evaluate alternative business solutions and strategies
  • Responsible for internal reporting on the status of the projects
  • Provide direction and support to the internal Oryzon staff collaborating at some point with the study
  • Collaborate with Business Development (BD) and Finance to ensure timely completion of CDAs, MSA, change orders
  • Track clinical operations project deliverables using appropriate tools
  • Manage the project budget: track budget deliverables using appropriate tools
  • Apart from the tight supervision of CROs and other clinical providers, the clinical operations team also works closely with internal clients in order to comply with internal processes, especially related to control of budget/orders/expenses/invoices and management of contracts with sites, CROs and providers.

¿A quién buscamos (H/M/D)?

  • Bachelor's Degree in medicine, science or equivalent degree.
  • At least 3 years' experience within clinical trials and study operations
  • Specific therapeutic experience in CNS and Oncology, will be desirable
  • Comprehensive knowledge of ICH-GCP is essential along with excellent communication, teamwork, planning, decision-making, negotiation, conflict management and time management skills
  • No travelling is expected
  • Proven fluent in written and spoken English is a must
  • Computer literate
  • Fluent in basic finance-control activities (i.e., elaboration of budgets; tracking of expenses and invoicing…)

¿Cuáles son tus beneficios?

  • Professional development and career planning
  • 100% Office Based (No home office available)
  • Flexible hours: 8-10 a.m. / 4-6 p.m., Monday through Friday
  • 15% bonus
  • Health insurance
  • 27 working days of free vacation
Ver más ofertas de empleo
Cristian Atik
Indicar número de referencia para la oferta
JN-042026-7002697

Resumen de empleo

Sector
Healthcare
Sub Sector
I+D
Añadir industria
Healthcare / Pharmaceutical
Localización
Barcelona
Tipo de Contracto
Permanente
Nombre del consultor
Cristian Atik
Número de referencia
JN-042026-7002697

En Michael Page creemos en la diversidad e inclusión. Defendemos la igualdad de oportunidades sin discriminar por género, raza, edad, religión ni orientación sexual o por cualquier otro aspecto que pudiera ser considerado excluyente.