Precision Medicine Group logo
Precision Medicine Group

Moving Science Closer to Health

Clinical Project Manager / Senior Clinical Project Manager

Clinical OperationsClinical OperationsFull TimeRemoteSeniorTeam 1,001-5,000Since 2012H1B SponsorCompany SiteLinkedIn

Location

Spain

Posted

20 hours ago

Salary

0

Seniority

Senior

Bachelor Degree4 yrs expExperience acceptedEnglishGoogle Cloud Platform

Job Description

Clinical Project Manager / Senior Clinical Project Manager

Precision Medicine Group

• Independently lead clinical projects in accordance with the study budget and scope of work. • Use your 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, informed 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 individuals 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

  • We offer an amazing high-energy, dedicated, collaborative team members who enjoy a challenge, thrive in the details and flourish in dynamic environments.
  • Supportive and collaborative environment which promotes work life balance and encourages team development.
  • Opportunity for growth and career development.
  • Positive teamwork to deliver extraordinary work.

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