Clinical Operations Lead: Start-Up & Site Activation

Adecco Portugal; Welwyn Hatfield; Híbrido; GBP 63.000 - 92.000; A tiempo parcial

Ventajas ofrecidas por este puesto de trabajo

Disability confident employer

Inclusive recruitment

Descripción de la vacante

Adecco Portugal is seeking a Clinical Operations Lead to steer study start-up activities, support regulatory submissions, and drive site activation across the UK. The role is hybrid (2-3 days in office) in Welwyn Garden City on a 6-month contract.

The ideal candidate holds a Life Sciences degree with proven clinical operations experience, UK submission expertise (IRAS, MHRA, HRA, Ethics), and strong ICH-GCP knowledge. Collaboration with global teams and vendors is essential.

Formación

• Degree in Life Sciences or related discipline.
• Experience in clinical operations or study start-up in pharma/CRO.
• Experience managing UK submissions through IRAS, MHRA, HRA.
• Knowledge of ICH-GCP, EU CTR, UK regulations.
• Experience from start-up to site activation.
• Exposure to site contracts and budgets.

Responsabilidades

• Lead country-level study start-up activities.
• Oversee trial submissions and approvals with MHRA, HRA, Ethics Committees.
• Drive site activation aligned with project timelines.
• Collaborate with global study teams, CROs, investigators and site personnel.
• Manage amendments through the clinical trial life cycle.
• Support site contracts and budgets.
• Maintain study documentation per ICH-GCP and EU CTR.
• Identify operational risks and mitigation strategies.

Conocimientos

Regulatory submissions

Site activation

ICH-GCP

UK regulations

Stakeholder management

Clinical operations

Educación

Degree in Life Sciences

Herramientas

CTIS

Veeva Vault

CPMS

Descripción del empleo

Adecco Portugal is seeking a Clinical Operations Lead to steer study start-up activities, support regulatory submissions, and drive site activation across the UK. The role is hybrid (2-3 days in office) in Welwyn Garden City on a 6-month contract.

The ideal candidate holds a Life Sciences degree with proven clinical operations experience, UK submission expertise (IRAS, MHRA, HRA, Ethics), and strong ICH-GCP knowledge. Collaboration with global teams and vendors is essential.