Medical Science Manager – Italy (International) – NSCLC

Medical Science Manager – Italy (International) – NSCLC

Amplity Health

Home Based, Italy

Purpose of Role

This role will be within an exciting US based Biotech that is developing novel therapies targeting the genetic and immunological drivers of cancer. You will be part of a new medical team in EU, that strives to be known for their credibility, tenacity and urgent focus to collaborate with all stakeholders and improve the lives of patients with cancer.

A professional with a strong oncology focus and background in scientific engagement, this individual will be the medical expert and point of contact within their assigned countries. An understanding of the healthcare system within your country and a treatment landscape, diagnostic testing and reimbursement and/or the ability to generate answers for provided questions related to these topics is important This is a highly valuable member of the Medical team who represents the company externally by engaging in highly credible scientific discussions with targeted thought leaders (TLs) and collaborates with clinical trial investigators to increase trial enrollment.

Key Accountabilities

Clinical Trial Support

  • Act as primary liaison to investigators interested in developing and performing investigator sponsored trials;
  • Engage with external experts on the generation of scientific data, including investigator – initiated studies;
  • Collaborate with clinical organization to enhance patient enrolment in company sponsored clinical trials by identifying appropriate trial sites and interacting with investigators in on going trials.;
  • Gather careful information from KOLs and report back to company to help develop clinical, as well as commercial strategy.

Scientific Expertise

  • Deeply understand the unique oncology treatment paradigm, key stakeholders, and healthcare landscape in your territory;
  • Develop and execute territory plans in alignment with medical strategy.

Opinion Leader Engagement

  • Identify, develop and maintain collaborative relationships with current and future Key Opinion Leaders (KOLs) and healthcare stakeholders in disease states of strategic importance to the company;
  • Provide medical and scientific information to respond to KOLs’ technical questions about the molecule/drug;
  • Represent client at select scientific congresses and professional society meetings;
  • Provide clinical presentations and information in response to unsolicited questions (as appropriate) in academic, and healthcare provider setting in both group and one on one settings.

Cross Functional Support

  • Assist as needed to local tactical activities (coverage of presentations at select scientific congresses, knowledge of contracting local consultants, etc.);
  • Assist in the reconnaissance of Market landscape determination and competitive intelligence including therapeutic trends and unmet needs within the appropriate disease states and marketplace and provide timely feedback/information on emerging clinical/scientific information to internal stakeholders.


  • Operate in a highly ethical manner and comply with all laws, regulations and policies;
  • Complete mandatory training in assigned timelines upon hire as well as when new policies, SOP’s, guidance are issued;
  • Adhere to internal standard processes and comply with regulatory and compliance requirements.


  • Doctorate level degree or equivalent experience is required (PharmD, PhD, MD, MSN);
  • Post graduate oncology experience is required with preference for experience working with lung cancer;
  • 3+ years of previous industry medical affairs experience required, preferably in MSL and/or headquartered based medical affairs role;
  • Knowledge ofhealthcare system and understanding of oncology treatment landscape, diagnostic testing and reimbursement in your country/assigned region;
  • Demonstrated expertise in building relationships and participating in credible scientific exchange with multiple audiences. Networking skills and confidence to interact with senior experts on a peer to peer level;
  • Experience with clinical trial design, conduct and evaluation;
  • Thorough knowledge of local (several countries or territory) legal, regulatory, and compliance regulations and guidelines relevant to industry interaction with health care professions;
  • Strong written and verbal communication skills, ability to present medical/scientific information in a clear and concise manner;
  • Ability to function well, both independently and within a team setting, in a dynamic, fast-paced environment. Team orientated and ability to work collaboratively towards common objectives;
  • Biotech experience is a plus;
  • Fluent in English and fluency in the language of a local country is required;
  • Able to travel internationally, up to ~50-70% of time.

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© EuroJobsites 2020

EuroJobsites is a registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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