Work with us


Are you interested in joining an international, high-level and fun team in the fascinating world of Clinical Research in Oncology? At MedSIR we are always on the lookout for top talent to help our business grow, whether in Business Development -looking for new strategic opportunities or internationally identifying new key players and bright talents in the field- or in Clinical Operations –helping to improve clinical research processes and identify top research centers worldwide. Although job positions vary at MedSIR, there is one thing that brings us all together: the will to help this battle against cancer and improve the lives of cancer patients and their families.

Also, you can check Our Vision and Core Values

Current Openings


International Trial Lead

If you are interested on this Job Position, please send us your CV

We are looking for an International Trial Lead (ITL) for a demanding yet very rewarding role in our company. The ITL 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.


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
  • Prioritizes signed-off project work based on analysis of strategic importance, outstanding tasks, obstacles or barriers, budgets, etc.


  • 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 organizational 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.

Senior Clinical Research Associate

If you are interested on this Job Position, please send us your CV

MedSIR is a private company dedicated to the design and management of strategic clinical trials in Oncology. We are looking to recruit a senior Clinical Research Associate (CRA) for our International studies. In this position you’ll be involved in all stages of the clinical trial, including identifying an investigational site and setting up, initiating, monitoring and closing down the trial.


  • Support the submission process in the project (or region), including submission requirements.
  • Organizes the study files and documents to ensure good start-up of the investigation sites.
  • Attend project coordination and study meetings as required.
  • Performs training site staff in all study procedures in order to ensure protocol/ICH-GCP compliance.
  • Conduct pre-study, initiation, monitoring and close-out visits.
  • Create monitoring reports, confirmation/follow-up correspondence and telephone contacts for assigned sites.
  • Guarantee traceability of all clinical trial documents and maintain clinical trial files, either in digital or paper.
  • Cooperates with the site staff for ensuring a proper reporting from the site of the safety issues (adverse events and adverse reaction such as AEs/SAEs, SUSARs, etc.) and their follow up.
  • Stay in contact with the site in order to ensure close follow up and keep updated information in study tracking.
  • Support the development of a subject recruitment plan.
  • Prepare, attend and respond to audit findings.
  • Communicating deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements to the investigator.
  • Verifying that source data/documents and other trial records are accurate, complete, and maintained.
  • Perform investigational product accountability and verify storage conditions.
  • Coordinate and organize the delivery o supplies as required.


  • Have experience working on Oncology clinical trial. Experience in Breast Cancer is desired but not mandatory
  • A university degree in a related field
  • 3 -5 years (at least) of experience as a CRA in that country
  • Excellent knowledge of clinical trial operations, GCP/ICH Guidelines and other applicable regulatory requirements
  • Fluent in English and local language(s)
  • Proficiency in Microsoft Office
  • Good digital skills, proficient with multimedia applications
  • Ability to work independently and with minimal supervision
  • Proactivity and communication skills
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