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Precision Medicine Group

Clinical Project Manager / Senior Clinical Project Manager

Precision Medicine Group

Clinical Project Manager/Senior Clinical Project Manager overseeing global clinical trials for Precision Medicine Group. Responsible for project delivery and collaboration with diverse teams in Oncology.

Posted 7/13/2026full-timeRemote • 🇷🇴 RomaniaSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates extensive project management expertise in clinical trials, particularly within Oncology, while ensuring compliance with GCP/ICH guidelines. Proven ability to lead cross-functional teams and maintain strong client relationships through effective communication and organizational skills.

Highest-signal resume keywords
Project ManagementClinical OperationsOncology Studies ManagementGCP/ICH GuidelinesClient Liaison

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial ManagementData ManagementMedical MonitoringBiostatisticsPerformance MetricsMedical TerminologyClinical Development Process
Soft Skills
Interpersonal SkillsOrganizational SkillsPresentation SkillsCustomer Service
Tools & Technologies
MS OfficeMS ProjectPowerPointCTMSETMFEDCIXRS
Industry Keywords
CRO IndustryClinical Research OrganisationClinical TrialsLife Science Qualification

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
  • 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
  • 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

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
  • Amazing high-energy, dedicated, collaborative team members who enjoy a challenge
  • Work life balance and encourages team development