Medical Science Manager - Lung Cancer - NSCLC

Medical Science Manager - Lung Cancer - NSCLC

Amplity Health

Italy

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.

Compliance

  • 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.

Qualifications:

  • 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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