Regulatory Compliance & Operations Executive

Planet Pharma; Bilbao; Híbrido; EUR 70.000 - 100.000; Jornada completa

Descripción de la vacante

A pioneering biopharma company focused on rare diseases is seeking a Senior Clinical Operations Project Manager. This role involves leading global clinical trials, managing vendor relationships, and ensuring regulatory compliance, providing an opportunity to contribute significantly to advancing therapies for underserved conditions. The position offers a hybrid working environment, allowing for both flexibility and autonomy.

Formación

• 7–10+ years of experience in clinical operations within biotech or pharma.
• Proven expertise in leading global trials, ideally in rare diseases or complex indications.
• Fluency in English; advanced degree preferred.

Responsabilidades

• Managing the full lifecycle of global clinical trials (Phases I–III).
• Overseeing CROs, vendors, and cross-functional teams.
• Ensuring compliance with GCP and maintaining audit-ready standards.

Conocimientos

Vendor Management

Risk-Based Monitoring

Regulatory Framework Navigation

Educación

Degree in Life Sciences

Descripción del empleo

Senior Clinical Operations Project Manager

Our Client : Global Biotech | Rare Disease Focus

Spain (Remote)

Role : Full-time, Permanent

Our client, a pioneering biopharma company dedicated to developing transformative therapies for rare and underserved conditions, is seeking a Senior Clinical Operations Manager to lead their global clinical trials with expertise and vision. We are proud to partner with them to find a strategic leader passionate about advancing clinical research that changes lives.

As a senior leader in our client’s Clinical Operations team, you will drive the success of cutting-edge global studies, shaping the future of rare disease treatments.

Managing the full lifecycle of global clinical trials (Phases I–III)

Overseeing CROs, vendors, and cross-functional teams to ensure delivery on time and within budget

Ensuring compliance with GCP and maintaining audit-ready standards

7–10+ years of experience in clinical operations within biotech or pharma

Proven expertise in leading global trials, ideally in rare diseases or complex indications

Strong skills in vendor management, risk-based monitoring, and navigating regulatory frameworks

A degree in life sciences (advanced degree preferred), with fluency in English

Work in a flexible, hybrid environment with autonomy

About Planet Pharma :

Planet Pharma is an American parented Employment Business / Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion / belief, sexual orientation or age.

Please click ‘apply’ or contact Finlay Keyworth (Recruiter II) at Planet Pharma for more information :