Medical Liaison-Oncology

KEY ACCOUNTABILITIES:
· Scientific communication with HCPs
1. Contacting HCPs to respon******** an unsolicite******** forinformation relating to a sanof******** t, therapeutic area, or diseasestate. Leaving behin******** reprint of anapprove********-reviewe********, slides sets or other materials.
2. Sharing information regarding new products or pipeline with HCPsin order to respon******** an unsolicite********. This information mayrelate to the agent’s mechanism of act******** relevant disease state******** review of phase II data an******** or ongoing clinical trials.
3. Providing product relate******** to regional speakers forsanof******** sponsore******** conference.
4. Responding to unsolicite******** from hosp******** healthcareorganizations or payers for assistance in the development an******** oftheir disease management an******** improvement initiatives that targetunmet medical needs an******** to a sanof******** or therapeutic area.
5. Develop scientific communication materials (e.g. slides kit ofhot top******** congress ******** etc.) for medical liaisons usagefollowing the review process in medical liaisons’ guideline.
· Medical an******** support to regional sales an******** team
1. Working closely with the regional BU colleagues, giving advice onthe strategic an******** regional base******** strateg******** ensuringinvolvement an******** of regional marketing an******** team.
2. Providing scientific training an******** answers to Marketingan******** personnels regarding sanof******** an******** diseasean******** therapeutic areas.
3. Participating in sanof******** sponsore******** conference,providing advice on scientific contents, communicating medicalinformation with speakers or cha******** answering questions onsanof******** with unbiase********.
· Collaboration with key opinion leaders (KOLs)
Developing an******** excellent professional relationships with KOLsin the responsible territory. Serve as key company liaison in thefiel******** KOLs to enhance scientific collaboration in clinicalresearch, medical e******** publ******** etc. .
· Clinical trial support
Supporting company sponsore******** investigator sponsore********trials by facilitating trial relate******** in the field.
· Compliance
Ensure all activities are in strict compliance with localregulat******** company policies an********, including but notlimite******** sanof******** of Con******** Goo******** PracticeGuidelines an******** Liaison Guidelines.

JOB-HOLDER ENTRY REQUIREMENTS:
1.Education:
Master of Medicine M.M. or more
2.Experience & knowledge:
At least 1-2 year clinical pract******** preferably in clinicaloncology
Industry experience in medical affa******** clinical development orclinical operation is preferred
3. Core competencie********
Information analytical skills an******** skills
4.Communication an******** skills
Able to work independently in the region an******** t********resource an******** under moderate travel frequency
Able to collaborate an******** partnership with internal (medicalmanagers, business unit) an******** key stakeholders (KOLs, payors)
Fluent in both written an******** English an******** PC skill.