Medical Monitor, Spain - L

07 Jan 2021
05 Feb 2021
Medical Affairs
Full Time
Contract Type
Experience Level
Experienced (non-manager)
CROMSOURCE is currently recruiting for a Medical Monitor (MEM) for an internal position, located in Poland or Spain.

Scope of the role:

The MEM provides clinical support to the CROMSOURCE internal Clinical Research Division (CRDIV) from study design to dissemination of the results.

Position Duties & Responsibilities:
  • Is clinical advisor for the entire life cycle of the clinical trial by answering to medical questions
  • Participates actively in the project meetings by giving his/her medical advice
  • Reviews study data listing from a medical point of view
  • Analyses and makes an independent interpretation of study data/results
  • Writes and/or reviews protocol, Case Report Form (CRF) and Clinical Study Reports (CSR)
  • Provides training in specific disease/therapeutic area

Education & Experience:
  • Qualified MD
  • At least 2 years of medical experience
  • Fluent in English and local language(s)
  • Proficiency in Microsoft Office (e.g. Word, Excel, Outlook)

  • Time Management and setting of priorities
  • Respecting of Deadlines
  • Multitasking
  • Proactiveness
  • Accuracy & Work in Detail
  • Stress Resistance
  • Flexibility
  • Written and verbal Communication skills
  • Teamwork
  • Positive attitude
  • Independence in your tasks
  • Self Confidence
  • Self-development / learning
  • Problem Solving
  • Customer Focus

The Benefits of Working for CROMSOURCE in Spain
  • Competitive Salary
  • Health insurance
  • Internet reimbursement
  • Dedicated Line Manager
  • Regular face-to-face or phone meetings with line manager
  • Full annual performance review process
  • End of year party with the team
  • Career opportunities within both our CRO departments and our TalentSource Life Sciences Unit, locally and internationally
  • Employee satisfaction survey - your feedback is important for continuous improvement

Who will you be working for?


CROMSOURCE is a family owned international, full-service Contract Research Organisation who, since 1994, has been supporting our clients with outstanding clinical research and staffing solutions services. The successful growth of CROMSOURCE has been achieved by putting high quality and client focus at the heart of everything we do.

Our Company Ethos

Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our below industry average turnover rates.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

If you would like to discuss the role before applying through the website @

or please contact for more information.

CROMSOURCE is an equal opportunities employer. All qualified applicants will receive consideration for employment in relation to race, colour, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran or military status or any other legally protected status. CROMSOURCE is also committed to compliance with all fair employment practices regarding citizenship and immigration status.

Keywords: Medical Monitor
Skills: Oncology, Respiratory, Medical Monitor, CSR, Drug Safety, Medical Devices, Medical Writing, Protocol writing Location: Spain Share:

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