Clinical Project Manager / Senior Clinical Project Manager

Precision For Medicine

Clinical Project Manager leading and managing full service clinical projects in Oncology. Collaborating with international teams for efficient trial management and delivery.

Posted 7/13/2026full-timeRemote • 🇪🇸 SpainSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive project management expertise in clinical trials, particularly within Oncology, while ensuring compliance with GCP/ICH guidelines. Proven ability to effectively communicate and build relationships with clients and project teams, driving successful trial execution.

Highest-signal resume keywords

Project ManagementClinical OperationsOncology ExperienceGCP/ICH GuidelinesMS Office Proficiency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementClinical Trial ManagementData ManagementMedical MonitoringBiostatisticsProtocol PreparationPerformance MetricsStudy DocumentationClinical Development ProcessMedical Terminology

Soft Skills

Customer ServiceEffective CommunicationPresentation SkillsRelationship BuildingTeam Collaboration

Tools & Technologies

CTMSETMFEDCIXRSMS ProjectPowerPoint

Industry Keywords

CRO IndustryClinical Research OrganisationClinical OperationsClinical TrialsOncology

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Independently lead clinical projects in accordance with the study budget and scope of work.
Serve as the primary point-of-contact liaison with the client to provide excellent customer service.
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 reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets.

Requirements

What you’ll need

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 individual 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.

Benefits

Comp & perks

Full service oversight for clinical projects
Supportive and collaborative environment which promotes work-life balance.