Job description


  • Entry level
  • No Education
  • Salary to negotiate


Job Description
1. Clinical Research: Review and prioritise study protocols in consultation with ICRO and MKT with respect to local MKT goals, scientific merit and ICRO resources. Advise ICRO on study sites and investigators and initiate first contact with potential investigators ; Contribute to international projects/trials via participation in the clinical team in the area of his/her expertise/subspecialty; Attend regular meetings to review ongoing trial progress and instigate appropriate measures ; Provide liaison between MKT and ICRO ; Provide interface with the local medical community both for local purpose and in support of international projects ; Build strong network with opinion leaders nationally, and with international colleagues in relevant therapeutic area ; Help to ensure that local adaptations to international trial plans and support documents are completed within the pre-defined time frame ; Provide local medical support at Investigator Meetings ; Provide input to clinical development plans, protocol summaries and protocols received from Basel ; Promote good communication and teamwork between Basel and the local office ; Review and co-ordinate local Phase IV and Investigator-Initiated protocols and forward to Basel for appropriate action and involve in scientific write-up of local Phase IV trials. 2. MKT : Provide Medical expertise to MKT colleagues in product development team from the development phase throughout the life of the product by ; Identifying the optimum positioning of the product in the life of the therapeutic area ; Identifying the potential customers within the medical community; Leading or contribution to KOL management including delivery of scientific agenda ; Participating in product launches & related meetings; Assisting in the evolution of appropriate promotional material ; Reviewing and approval of promotional material, etc ; 3. General : Assist the CSO in projecting a credible medical image for Novartis in the health care and research communities ; Provide medical expertise to KFDA requirements ; Comment to Clinical Expert Report if relevant to expertise ; Provide medical training to within medical function and cross-function on Novartis' and competitors' drugs, as well as on target indications ; Respond to medical issues & enquiries related to marketed products by the medical community ; Support DRA, DS&E, Medical Information with medical input ; 4. Comply with NP4 & G3 guidelines
Minimum requirements
Graduated medical college Upper middle level of English proficiency At least 5 years of experience in medical (or equivalent) field after Medical License

Division PHARMA
Business Unit AMAC
Location South Korea
Site Seoul
Company/Legal Entity NOV KOR
Functional Area Research & Development
Job Type Full Time
Employment Type Regular

About the company

Novartis has a clear mission, focused strategy and strong culture, all of which we expect will support the creation of value over the long term for our company, our shareholders and society. We recognize that our business depends on the creativity, dedication and performance of our associates. We encourage associates to focus on achievement through collaboration and innovation.

A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewarding employers in our field.

Our company culture is guided by high ethical standards. Our values help guide the choices people make every day, and they define our culture and help us execute the Novartis strategy in line with our mission and vision.


Companies in this sector

Hives where you can find this job offer