Senior Manager, Quality Operations

buscojobs España; Madrid; Híbrido; EUR 80.000 - 120.000; Jornada completa

Descripción de la vacante

A global biopharma company is seeking a Senior Clinical Operations Project Manager to lead their clinical trials focused on rare diseases. This full-time, permanent role offers the opportunity to manage global studies, ensuring compliance and excellence in execution within a flexible hybrid environment.

Formación

• 7-10+ years of experience in clinical operations within biotech or pharma.
• Proven expertise in leading global trials, ideally in rare diseases.
• Fluency in English is required.

Responsabilidades

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

Conocimientos

Vendor management

Risk-based monitoring

Regulatory frameworks

Educación

Degree in life sciences

Advanced degree preferred

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 :

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