ITALY – Freelance Clinical Project Manager

Job Type: contract
Sector: Clinical
Job Category: Project Manager
Region: Europe
Area: Italy
Location: Unspecified
Salary: Competitive hourly rates
Posted: April 4, 2017
Ref: MTMRFCPMIT-04-04

ITALY – Freelance Clinical Project Manager – Cardiovascular Specialist – 12 month contract – 1.0fte

I have partnered with a European client working across the globe specialising in Cardiovascular products. My client is looking for one highly experienced Freelance Clinical Project Manager within Italy. The right candidate will benefit from a long term contract with high chances of extension every 12 months due to their pipeline.

 

PRIMARY DUTIES 

Identifies project guidelines and communication needs by:

  • Reviewing study requirements and response assessment criteria and collaborates with key stakeholders to develop study start-up activities and associated documents
  • Establishing clear and measurable project operating guidelines with Director of Clinical Research and relevant representatives
  • Defining project plans (i.e. timelines, milestones and limitations for project staff)
  • Establishing project reporting schedules with Director of Clinical Research and relevant representatives
  • Providing project updates to Director of Clinical Research and relevant representatives on schedule
  • Communicating timely, appropriate project information to project teams, sites and company/sponsor representative(s)

Performs project analysis and management by:

  • Identifying critical project success factors for tracking, analysis and reporting
  • Determining needed resources for project completion and communicating needs to appropriate departmental managers
  • Collaborating with department leaders for appropriate training of those involved with the project toward excellence in successful and timely completion of project
  • Developing budget and expense review strategy
  • Creating proactive cost containment strategies and communicating them to project team
  • Reviewing regularly the task/time budget and expenses with team
  • Understanding SOPs and working closely with QA for clarification and documentation of deviations
  • Training and maintaining project team knowledge and applications of SOPs
  • Communicating all protocol clarifications/revisions to project team
  • Coordinating site management of data collection with internal and external teams
  • Possessing a thorough understanding of the project contract and totals needed for monthly revenue reporting
  • Managing pass through expenses associated with the project

Required Experience:

  • Life science degree
  • Previous management or project experience in clinical development of investigational medications, Cardiovascular and other indications beneficial
  • 5+ years within Cardiovascular
  • 5+ years clinical trials or project management experience within a CRO or pharmaceutical research organization required; preferably in a project management related role
  • Working knowledge of GCH, ICH guidelines and FDA regulations
  • Experience working with computer software including Word, Excel, Access and Project preferred

 

 

Required Skills:

  • Strong interpersonal and communication skills, both verbal and written
  • Strong organizational and leadership skills
  • Goal oriented
  • Ability to maintain professional and positive attitude

 

For further information about this role and to be considered as an applicant, please get in touch with Matias Martin-Baeza at mmbaeza@barringtonjames.com or call +44 1293 776644

About Your Consultant

I primarily focus on the European Clinical market specialising in freelance interim contracts.

Email: mmbaeza@barringtonjames.com Telephone: +44 1293 776644

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