Clinical Project Manager

Precisionmedicinegroup; España; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

Precision Medicine Group is seeking an experienced Senior Project Manager in Oncology to oversee full-service clinical trials across global/regional scopes (Phase I–IV). You will manage timelines, budgets, and cross-functional teams while maintaining high standards of quality and regulatory compliance.

The role requires strong client management, leadership, and communication skills, with willingness to travel domestically and internationally to drive study success.

Formación

• Degree or life sciences qualification required.
• Experience leading full-service/global PM roles in CROs essential.
• 5–7 years in clinical trial project management, oncology focus.
• GCP/ICH knowledge and clinical development process familiarity.

Responsabilidades

• Lead full-service clinical projects across global/regional trials (Phase I–IV).
• Oversee cross-functional teams and manage client relationships, budgets, and timelines.
• Ensure delivery within scope, cost, and quality.
• Prepare study documentation, protocols, and feasibility/proposal activities.

Conocimientos

Interpersonal skills

Organizational skills

Presentation skills

Client management

Cross-functional collaboration

Educación

Life science degree

Herramientas

CTMS

eTMF

EDC

IXRS

MS Office

MS Project

PowerPoint

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 are looking to hire a (Senior) 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. 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, and seeing 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.

How we will keep you busy and support your growth

• You will independently lead clinical projects in accordance with the study budget and scope of work. You will use your strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and 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
• Handle and lead all aspects of a clinical research trial or trials
• 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; identifying 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, informed 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.
• 5 to 7 years industry experience 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 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.