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Medical Advisor

  • Health Data Specialists (HeaDS)
  • Αθήνα
  • 4/5/2018

Στοιχεία αγγελίας

Σχέση απασχόλησης - Πλήρης ΑπασχόλησηΕλάχιστη Απαιτούμενη Εκπαίδευση - ΜεταπτυχιακόΑπαιτούμενη Προϋπηρεσία - Τουλάχιστον 3 έτος/ηΚατηγορίες - Επαγγέλματα Υγείας

Περιγραφή

Medical Advisor/Code: MA

Health Data Specialists (HeaDS), an Athens based CRO with a global reach, is seeking a Medical Advisor for its international Clinical Trials program.

As a Medical Advisor at HeaDS you are a highly educated individual ready to undertake projects of high complexity and able to provide scientific input in Clinical Trials across multiple Therapeutic Areas (key focus on Oncology/Hematology).

Required Qualifications:
• Advanced  degree in Health Sciences (e.g. MD, PHD etc.) is a must
• Combination of health science and engineering/quantitative background is highly desirable
• Previous Work Experience: 
o Minimum 3 years’ work experience in the Pharmaceutical Industry in Medical Affairs/R&D positions
OR
o Minimum 3 years’ work experience in consulting firms with exposure to pharmaceutical projects
OR
o Qualified Medical Doctor (Oncologist, Hematologist, Internist preferred)

• A deep understanding of all aspects of the Pharmaceutical field
• Oncology/Hematology experience will be highly appreciated
• Ability to present complex content to key audience and engage in daily professional conversation in English 
• Initiative taking and team working attitude
• Innovative thinking and excellent organizational skills
• Strong attention to detail
• Ability to work under pressure with a results driven attitude
• Very strong written and verbal communication skills in both Greek and English

Main responsibilities:
• Directly reports to the Medical Affairs Lead
• Leads all medical tasks of the assigned clinical trial
o Undertakes Medical Writing tasks (Protocol, CSR, Manuscripts etc.)
o Performs Medical Data Review in the context of a Clinical Trial
• Acts as a medical expert within the company for assigned Therapeutic Area (TA)
o Develops and delivers internal and external Protocol/Therapeutic Area trainings 
• Provides guidance to HeaDS Project Managers on the TA specific medical and scientific aspects of a clinical trial
• Available 24/7 to respond to urgent medical/protocol related issues at the investigational site.
Join us to be part of a multidisciplinary team of highly skilled professionals in the forefront of Clinical Research within a friendly work environment. Competitive remuneration package comes on top.

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