Clinical Project Manager

buscojobs España; La Coruña; A distancia; EUR 50.000 - 80.000; Jornada completa

Descripción de la vacante

A growing biotech company is seeking a Clinical Project Manager to oversee global clinical trials. This remote role requires extensive experience in clinical project management, excellent leadership and communication skills, with a focus on regulatory compliance. Join a passionate team that values collaboration and innovation in a dynamic medical environment.

Servicios

Flexible remote-first working setup

Competitive compensation and benefits

Formación

• Solid experience in clinical project management, focusing on global trials.
• Excellent understanding of clinical development and regulatory guidelines (ICH-GCP).
• Must be EU-based and eligible to work in the EU.

Responsabilidades

• Manage the full lifecycle of global clinical trials, including planning, execution, and close-out.
• Lead cross-functional teams and oversee third-party vendors.
• Ensure compliance with ICH-GCP, monitor project timelines, budgets, and risks.

Conocimientos

Clinical project management

Leadership

Communication

Organizational skills

Regulatory guidelines understanding

Descripción del empleo

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

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.