Medical Manager

Medical Manager

 

Key responsibilities: 

  • Provide medical training to company’s employees when needed
  • Medical Advisor activity for the clinical studies conducted by the Company (e.g. medical support in the drafting of protocols and reports, in the review of clinical data and in the interpretation of product safety data)
  • Close collaboration with the Head of Clinical Operations and with the Scientific Director
  • Cooperation with Clinical Operations, Data Management, Biostats, and Medical writing Units
  • Manage with a positive and proactive attitude the current and the future customers by taking care of their relationship with continuous contacts, and collaborating in the identification of new studies
  • Contribute to company growth
  • Timely inform the Company of the requests coming from the market, in order to identify any unsatisfied/partially satisfied needs specific for clinical development
  • Participate to meetings or conferences in the medical-scientific field, on the occasion of which meeting current or potential customers, with the aim of both strengthening relationships and expanding the network of knowledge and contacts
  • Participate as a speaker in initiatives of 1Med and of various industry associations with the aim of increasing the visibility of 1MED
  • Participate in the activities of collaborative groups or specialist associations in areas where 1MED has considerable expert

 

 Candidate ideal requisites:

  • MD, with possibly a high degree mark
  • At least 3-5 years of experience in a similar position gained at Pharma, or Biotech or CRO companies (preferential requisite), or previous experience in the clinical development of medical devices gained at Pharma, or Biotech or CRO companies (alternative requisite)
  • Specialisation degree in Oncology, Immunology, Pharmacology, is considered a plus
  • Previous Clinical (Hospital) and Clinical Research experience in Advance therapies and/or Gene therapy will be considered a plus
  • Previous experience in pre and post-approval clinical research phases is a mandatory requisite
  • Knowledge in clinical trial methodology is mandatory, while knowledge in biostatistics and in regulatory affairs is desirable 
  • Excellent communication and negotiation skills, positive interaction capability with clients, KOLs, Institutions, and with the CRO staff is also a relevant need for the position
  • Reliability, loyalty, seriousness, problem solving and proactive attitude, teamwork and common sense approach are also key requisites
  • Advanced knowledge of English language spoken and written (mandatory requisite), knowledge other languages (considered a plus)
  • Availability to live in the area where the CRO headquarter is located 
  • Availability to travel according to company and client needs.

 

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REGULATION (EU) 2017/745

REGULATION (EU) 2017/745