Clinical Project Manager / Senior Clinical Project Manager

Clinical OperationsClinical OperationsFull TimeRemoteSeniorTeam 1,001-5,000H1B No SponsorCompany SiteLinkedIn

Location

Romania

Posted

6 hours ago

Salary

0

Seniority

Senior

Bachelor Degree4 yrs expEnglishGoogle Cloud Platform

Job Description

Clinical Project Manager / Senior Clinical Project Manager

Precision For Medicine

• 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 reviews protocols and other study documentation such as project plans, inform consents, site contracts and budgets

Job 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.
  • 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

  • Remote work options
  • Supportive and collaborative environment

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