Clinical Project Manager

buscojobs España; Asturias; A distancia; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

A leading biotech company is seeking a Clinical Project Manager to oversee global clinical trials. This remote position requires solid experience in project management and offers a flexible work setup. Join an innovative team making real impacts in the biotech field, with competitive compensation and a collaborative environment.

Servicios

Flexible remote-first working setup

Competitive compensation and benefits

Formación

• Solid experience in clinical project management with a focus on global trials.
• Excellent understanding of clinical development and regulatory guidelines.
• Must be EU-based and eligible to work in the EU.

Responsabilidades

• Manage the full lifecycle of global clinical trials including planning and execution.
• Lead cross-functional teams and oversee vendor relationships.
• Ensure compliance with regulations and monitor project timelines and budgets.

Conocimientos

Project Management

Communication

Leadership

Organizational Skills

Educación

Experience in clinical project management

Understanding of ICH-GCP

Descripción del empleo

Job Title : Clinical Project Manager (Global Clinical Trials)

Location : Remote based in Spain

Employment Type : Full-time

We are currently recruiting on behalf of our client, an exciting and growing biotech company focused on bringing innovative therapies to market. As part of their continued expansion, they are looking for a Clinical Project Manager to join their global team and lead international clinical trials across multiple regions.

This is a remote-based role open to candidates located anywhere in the European Union .

About the Role :

In this role, you will be responsible for overseeing global clinical study operations from start-up through close-out. The ideal candidate will bring proven experience in managing international clinical trials and will thrive in a fast-paced, agile biotech environment. You’ll work closely with cross-functional teams, CROs, and vendors to ensure successful execution of studies in line with timelines, quality standards, and regulatory expectations.

Key Responsibilities :

Manage the full lifecycle of global clinical trials , including planning, execution, and close-out

Lead and coordinate cross-functional teams, both internally and externally

Oversee third-party vendors and CRO relationships to ensure study deliverables

Ensure compliance with ICH-GCP, SOPs, and all applicable regulations

Contribute to the development and review of study protocols and operational documents

Monitor project timelines, budgets, and risks, implementing mitigation plans as needed

Serve as the primary point of contact for internal stakeholders and external partners

Candidate Profile :

Solid experience in clinical project management , with a focus on global trials

Excellent understanding of clinical development and regulatory guidelines (ICH-GCP)

Strong communication, leadership, and organizational skills

Comfortable working remotely in a dynamic, matrixed environment

Must be EU-based and eligible to work in the EU

Desirable (Nice to Have) :

Experience in neuroscience or ophthalmology

Previous exposure to both early and late-phase trials

Why Join?

Work with a biotech company that values innovation, transparency, and collaboration

Be part of a passionate, mission-driven team

Flexible remote-first working setup

Competitive compensation and benefits

If you're looking to take the next step in your clinical career with a company where you can make a real impact, we’d love to hear from you.

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.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including : 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.