Clinical Project Manager / Senior Clinical Project Manager

Precision For Medicine; Madrid; Presencial; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

Precision for Medicine is seeking an experienced Clinical Project Manager / Senior Clinical Project Manager with oncology trial leadership. You will oversee full-service trials globally, manage client relationships, and coordinate cross-functional teams across data management, safety, medical monitoring, and biostatistics.

This role requires CRO background, GCP/ICH knowledge, travel readiness, and strong English communication; join a high-energy team delivering innovative cancer therapies.

Formación

• Degree or life science qualification, or equivalent combination of education and experience.
• Previous experience in a full-service/global Project Management role in the CRO.
• At least 4 years full-service PM experience in a clinical trial setting for a CRO.
• Experience managing studies within Oncology.
• GCP/ICH knowledge and clinical development process understanding.
• Willingness to travel domestically and internationally.
• Fluent English language communication (written and spoken).
• Strong presentation skills.
• Proven computer skills: MS Office, MS Project, PowerPoint; CTMS, eTMF, EDC, IXRS.
• Ability to build positive working relationships with internal and external teams.
• Understanding of medical terminology and clinical trial activities in development plans.

Responsabilidades

• Lead clinical projects independently within the study budget and scope; may run international trials.
• Serve as the primary client liaison, supporting proposals and client presentations.
• Liaise with Project Team and senior management, including sponsors and C-level stakeholders.
• Handle and lead all aspects of a clinical trial; total project management across multiple functions.
• Prepare project status updates; identify deliverables and performance metrics.
• Contribute as an active Project Team member for efficient trial management.
• Prepare and review protocols and study documents such as plans, consents, site contracts and budgets.

Conocimientos

Project management

Stakeholder management

Team leadership

English proficiency

Presentation skills

Client liaison

Educación

Life science degree

Equivalent education/experience

Herramientas

MS Office

MS Project

PowerPoint

CTMS

eTMF

EDC

IXRS

Descripción del empleo

Are you an experienced full service Project Manager in the field of clinical trials who’s engaged in addressing the challenges facing the research and development of novel compounds in Oncology? Are you passionate about impacting the health and lives of patients around the world? Do you take a consultative approach to trial management, proving to be a valuable partner in trial operational delivery?

Precision for Medicine is looking to hire a Clinical Project Manager / Senior Clinical Project Manager with experience in Oncology who has managed full service clinical trials within a CRO setting to join our global team.

In this pivotal role you will have full service oversight for clinical projects across global/regional (Phase I-IV) trials within Oncology. You will be accountable for clinical project delivery, oversight of all functional departments, and ensuring agreed timelines, scope, cost and quality.

Involved in all study stages, including proposal strategy, development, costing, and bid defence, you will see studies through the full cycle to completion, managing the client relationship, project team and budget and timelines throughout.

You will work in a cross‑functional team with both internal and external stakeholders, driving quality and coordinating the study team.

We offer an amazing high‑energy, dedicated, collaborative team environment where team members thrive on challenge, detail and dynamic conditions. If you are no stranger to taking charge and seek positive teamwork to deliver extraordinary work, we have an opportunity for you.

We will keep you busy and support your growth

• Independently lead clinical projects in accordance with the study budget and scope of work; use strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects, including financial objectives. You may be called upon to run international trials as well.
• Serve as the primary point‑of‑contact liaison with the client to provide excellent customer service, including participation in proposal activities and client presentations.
• Liaise with Project Team and senior management of both Precision and sponsors, including C‑level stakeholders.
• Handle and lead all aspects of a clinical research trial or trials.
• Own total project management for all functional areas including data management, safety, clinical, medical monitoring and biostatistics, etc.
• Prepare project status updates for clients and management; identify key deliverables and performance metrics of success and escalation.
• Serve as an active member of the Project Team with the goal to contribute towards efficient management and execution of trials.
• Prepare and review protocols and other study documentation such as project plans, information consents, site contracts and budgets.

Requirements

• Degree or similar related life science qualification, or equivalent combination of education and experience.
• Previous experience in a full‑service/global Project Management role working in the CRO industry is essential.
• Extensive experience working within Clinical Operations position within a CRO, and at least 4 years full‑service Project Management experience in a clinical trial setting working for a Clinical Research Organisation.
• Experience managing studies within Oncology.
• Working understanding of GCP/ICH guidelines and the clinical development process.
• Ability to drive and availability for domestic and international travel including overnight stays.
• Be able to communicate effectively in the English language, both written and spoken.
• Strong presentation skills.
• Proven computer skills (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS).
• Proven ability to develop positive working relationships with individuals and teams internally and externally.
• Demonstrated core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan.

Precision for Medicine's uniquely integrated offering enables the science of precision medicine by combining novel clinical trial designs, industry‑leading operational and medical authorities, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology.

We are a people‑focused CRO with a supportive and collaborative environment that promotes work‑life balance and encourages team development.

We invite you to learn more about our growing organization serving our clients that are researching ground‑breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day.

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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [e-mail].

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