Clinical Project Manager / Senior Clinical Project Manager

Precision Medicine Group

Clinical Project Manager leading full-service clinical trials at Precision Medicine Group. Managing budgets, timelines, and client relationships across global oncology projects.

Posted 7/13/2026full-timeRemote • 🇸🇰 SlovakiaSeniorWebsite

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. Exhibits strong interpersonal and organizational skills to effectively liaise with clients and manage project deliverables.

Highest-signal resume keywords

Project Management ExperienceClinical Operations ExpertiseOncology Study ManagementGCP/ICH Guidelines KnowledgeClient Liaison Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Project ManagementClinical Trial ManagementData ManagementMedical MonitoringBiostatisticsProtocol PreparationBudget ManagementPerformance Metrics IdentificationStudy Documentation ReviewClinical Development Process

Soft Skills

Interpersonal SkillsOrganizational SkillsCommunication SkillsPresentation SkillsRelationship Building

Tools & Technologies

MS OfficeMS ProjectPowerPointCTMSETMFEDCIXRS

Industry Keywords

Clinical Research OrganisationCRO IndustryClinical OperationsOncologyGCPICHClinical Development PlanStudy BudgetProject ScopeClient Presentations

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.
Use strong interpersonal and organizational skills to set and achieve objectives in the execution of the projects; both contracted objectives and financial objectives.
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 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

Work life balance
Collaborative environment
Professional development support