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Precision for Medicine

Clinical Project Manager / Senior Clinical Project Manager

RemotePoland only
Published
Role
Project Management
Experience
Senior
Salary not disclosed
Check eligibility

Open to PL only. Set where you work from to check your eligibility.

No BS summary

Experienced full-service Clinical Project Manager or Senior Clinical Project Manager for oncology clinical trials in a CRO setting. Must be based in Poland/remote, have 4+ years full-service clinical trial project management, strong GCP/ICH knowledge, English, and ability to travel.

Core skills

Clinical trial project management

Required skills

GCPICHMS OfficeMS ProjectPowerPointCTMSeTMFEDCIXRS

Required languages

English written and spoken communication required; level not specified ंomidou

What you'll do

  • 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 projects, including contracted objectives and financial objectives.
  • Run international trials when called upon.
  • 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.
  • Provide 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 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.
  • Manage the client relationship, project team, budget and timelines throughout the full study cycle.
  • Work in a cross-functional team with internal and external stakeholders, driving quality and coordinating the study team.

What they require

  • 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.
  • Experience managing full service clinical trials within a CRO setting.
  • Experience in Oncology.

Benefits

  • Supportive and collaborative environment which promotes work life balance.
  • Encourages team development.
  • Employees feel appreciated for the contributions they make every single day.

Clinical Research

HealthcareEnterpriseprecisionformedicine.com/

What people say about this company

2.8/ 5

Details

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Salary not disclosed