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Medical Science Liaison - Oncology

Company Tardis Medical Consultancy
Location New York, NY
Update 9 Day ago
300

Medical Science Liaison

Oncology – Solid Tumours

North East USA

  • Contract: At Will (W2) with Tardis Medical - with potential to go perm
  • Duration – Initial 12 months with potential to go perm
  • $140-160 000 annual salary plus benefits, bonus and health
  • Travel: 60% inter-State travel
  • Location: Work from home NE USA
  • Territory: Northeast of the US, with a larger focus on the following states: Massachusetts, Pennsylvania, New York, New Jersey, Virginia and Washington DC.

The MSL role focuses primarily on providing scientific, clinical, economic and educational support to healthcare professionals (HCPs) at clinical trial research sites (Principal Investigators ((PIs)) and their study teams) in addition to national and regional KOLs who have a key influence in the digestive oncology community; therefore, strong experience and pre-existing advanced knowledge of working in oncology- solid tumours, cholangiocarcinoma, lung, digestive, pancreatic, would be necessary.

ACCOUNTABILITIES:

  • Deliver client product to specific physicians and their support staff (develop client’s presence in US)
  • Provide accurate and non-promotional scientific information relating to pipeline compounds to specific study sites and their associated referral networks.
  • Answer medical/technical enquiries, related to pipeline compounds and/or clinical trial design/rationale, from PIs/study site team members using in-house developed and approved resources.
  • Keep up to date with clinical knowledge, published data and trial work for client and competitive haematology product studies,
  • If requested, support relevant education at Site Investigator Meetings (SIMs) in line with clinical study plans
  • Develop strong communication links with PIs and study physicians and their teams.
  • Ensure requests received from PIs are managed efficiently and effectively, and that the client studies are the primary focus of the study site support teams.
  • Act as field-based reference point of scientific and clinical expertise for study sites and CRO.
  • Alignment between client and CRO study project teams to ensure synergies occur between them and that all field based clinical activities achieve global study team goals
  • Liaise closely with EU Medical Affairs department and monitor study performance
  • Support of ongoing and future company sponsored trials
  • Liaison between corporate clinical operations and study sites e.g., visit trial centres as required to provide updates on study compound and maintain client presence and enhance enrolment rate.
  • Identify additional trial centres for future trials for all client pipeline products
  • Respond to requests for investigator-sponsored research in line with company procedure
  • Build on the image and professionalism of client in Europe

EDUCATION, EXPERIENCE, SKILLS, KNOWLEDGE

Education:

  • Physician, Pharmacist, PhD in a relevant scientific field
  • Fluent written and spoken English (mandatory).

Experience:

  • Minimum 3 years relevant experience in pharmaceutical industry
  • MSL/CTML experience
  • Solid tumour oncology experience must/very good to have – Cholangiocarcinoma, Lung, Digestive, Pancreatic oncology ideal
  • Experience in management of KOLs, Researchers and HCPs at all levels in both 1:1 and group settings
  • Experience of working within the relevant National Pharmaceutical Code

Knowledge:

  • In-depth knowledge of the applicable GXP regulations, Good Clinical Practices, ICH Guidelines and National Code of Practice
  • Understands the overall audit process including design, conduct and reporting

Please apply with an up to date CV detailing the required experience above.

Job Type: Full-time

Salary: $140,000.00 to $160,000.00 /year

Required education:

  • Doctorate

Required experience:

  • Oncology: 1 year
  • Medical Science Liaison: 2 years