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European MSL Oncology

JOB SUMMARY

We are currently looking to fill a position for a European MSL (home-based) for a duration of at least 2 years to collaborate in an exciting pan-European phase III trial in Oncology.

DESCRIPTION

  • Maintain bilateral communication and solid professional relationships between site PIs, investigator teams, KOLs and the company’s medical department to support the medical/scientific information and research needs.
  • Develop and conduct training sessions on scientific/medical information at specific training events and site initiation visits
  • Provide medical protocol and safety training to clinical investigators/investigational sites and to any site staff involved in the trial. 
  • Participate in the routine review of protocol medical deviations, identify the possible root cause(s) of common deviations and evaluate the need of additional training and/or support for investigational/clinical site staff and, if necessary, deliver. For those protocol deviations that may have an impact in subject’s safety, discuss and give support to any immediate actions required.
  • Participate in team meetings, Data Monitoring Committee and Steering Committee or any other kind of project meetings, if required.
  • Assist in SIVs, training all members of the site research team on product and protocol.

SKILLS AND QUALIFICATION:

  • Experience in Oncology, preferably Lung Cancer.
  • At least 3 years of clinical research experience.
  • Familiarity with the scientific community and the medical research process.
  • Strong interpersonal, communication, facilitation and presentation skills.
  • Ability to work collaboratively with colleagues across all functions and at all levels.
  • Demonstrated ability to establish and maintain effective relationships and parternships with investigators.
  • Strong analytical and problem solving skills.
  • Excellent analytical, presentation, writing and computer skills.
  • Working knowledge of regulations, GCPs, etc.
  • Ability to communicate effectively in English. Other local European languages are a plus.
  • Excellent organizational skills with demonstrated ability to work well in a deadline driven environment.
  • Maintain a problem-solving attitude in response to time demands and unexpected events as working tasks by objectives.
  • Ability to travel as required to support Site Initiation Visits and other outreach activities and international meetings.
If you are interested on this Job Position, please send us your CV

International Project Manager

JOB SUMMARY

We are looking for an International Project Manager (IPM) for a demanding yet very rewarding role in our company. The IPM will report to the Director of Project Operations. The position’s main objective will be to fully carry out international MedSIR-sponsored clinical trials in the pre-established time frames, as well as controlling the costs and quality of the studies assigned.

DESCRIPTION

Internal project reporting and administration: • Be prepared to discuss project quality, client and team satisfaction, and project success metrics during regularly scheduled and ad hoc project review meetings with the Director of Project Operations. • Keep an accurate risk-tracking record with associated mitigation plan. Resource management • Determine project roles of team members based on project requirements, timeframes and budget. • When necessary work with external contractors in addition to internal resources. • Define skill sets (competencies) required for the project based on project specifications and requirements. Client management • Continually seeks opportunities to increase customer satisfaction and strengthen client relationships. • Manages day-to-day client interaction. Project accounting and finance • Accurately forecasts revenue, profitability, margins, bill rates and utilization. • Tracks and reports team hours and expenses on a weekly basis. • Manages project budget. Project planning • Prioritises signed-off project work based on analysis of strategic importance, outstanding tasks, obstacles or barriers, budgets, etc.

SKILLS AND QUALIFICATION:

  • A university degree in a related field
  • Based in the EU
  • Fluent in English, both oral and written
  • Demonstrated ability to establish and maintain effective relationships and partnerships with key stakeholders
  • Strong interpersonal, communication, facilitation and presentation skills
  • Strong analytical and problem solving skills
  • Ability to work independently and with minimal supervision
  • Demonstrated ability to work in a small team setting
  • Good computer skills, proficient with ms office applications
  • Ability to communicate effectively other EU languages is an asset
  • Excellent organisational skills with demonstrated ability to execute projects on time and on budget
Required languages: Fluent in English, knowledge of other EU languages would be highly valued. Minimum professional experience required: 5 years in Clinical Trial Project Management, preferably in Oncology If you are interested on this Job Position, please send us your CV

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