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AbbVie Medical Science Liaison in Hangzhou, China

Medical Science Liaison

China, Zhejiang, Hangzhou

Medical

Requisition #2000832

JOBSUMARY/ AND PRIMARY OBJECTIVE :

The role of MSL focuses on medical and scientific engagement with AbbVie stakeholders (including healthcare professionals (External Experts,EE), payers, and care-givers) by face to face scientific dialogue and scientific collaborations in research and other abbvie sponsored or institution sponsored projects. MSL work collaboratively and cross-functionally with other in-field members while retaining functional independence and Non-promotional nature.

CORERESPONSIBILITIES:

Scientific engagement of External Experts

Responsible for identifying, developing, and maintaining relationships with external experts (EE) in a given therapeutic area through: peer-to-peer scientific interaction and discussion of relevant AbbVie clinical/scientific information.

Responsible for summarize and report Field Scientific insights(FSI) from EE and acting as scientific liaison between AbbVie and the EE (eg, to interface with AbbVie investigators, understand clinical practice, collaborate on projects to improve standards of care, including early access programs (compassionate use) as appropriate.

Non-promotional Scientificactivities

Responsively and timely communicate unsolicited requests from HCPs on off-label and pre launches products and clinical trials updates.

Facilitate of research grant and continuous medical educational in the field.Can facilitate Abbvie research and educational priorities and strategic initiatives.

Assist in the initiation, oversight and follow up of Abbvie sponsored clinical studies(e.g. Phase III clinical trials, post marketing clinical activities such as registry/database projects, epidemiological surveys, post-authorization studies ,phase IV interventional studies). All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and AbbVie R&D (GPRD) SOPs.

Act as the point of contact with external experts to facilitate investigator initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate.

Scientific Presentations andpublications

Serve as a point of contact within the Medical Affairs team for external experts and external experts within an assigned geographic area in order to satisfy their needs for scientific knowledge in a therapeutic area and, when requested, relevant AbbVie medicines, to support their safe, effective and appropriate use.

Deliver credible presentations on scientific matters to physicians, individually or in groups (meetings, clinical sessions, etc.), where requested, but with the focus on Tier 1, 2 and 3 external experts.

Attend relevant scientific meetings and Conferences. Collaborate with internal stakeholders to develop summaries of key data and other scientifically relevant information to inform Abbvie strategic priorities and initiatives.

Provide key external experts / external experts and internal medical and clinical teams with scientific and technical support for publications of scientific or medical interest.

Compliance and InternalCollaboration

Ensure that all activities and interactions are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice.

Support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update Trainings and Frequently asked questions(within Label in the china).

Develop and maintain collaborative relationships with external experts in the product / therapeutic area for which the MSL has been assigned responsibility,

  • Master oradvance degree in Medical/Pharma qualification, Relevant TA experience in clinicalpractice is preferred. Or Bachelor degree major in clinical medicine, pharmacology,prefer to have strong medical background or more than 2 year clinicalexperience in relevant therapeutically area.

  • Solidknowledge of the pharmaceutical environment and the role of Medical Affairs toadvance the medical and scientific objectives of a pharmaceutical company.

  • Records onGCP training and other GXP trainings, a training or understanding code ofindustry such as RDPAC Code is preferred.

  • Excellent writtenand spoken communication and presentation skills, with a demonstrated abilityto develop and maintain strong collaborative relationships with externalexperts, physicians and other healthcare decision makers.

  • A goodunderstanding of written and oral English is desirable.

  • High customerorientation and willingness for collaboration and helping others.

  • Strongcommitment to compliance with the relevant rules and procedures, and toscientific quality and integrity

Additional Information

  • Travel: Yes, 50 % of the Time

  • Job Type: Experienced

  • Schedule: Full-time

  • Job Level Code: IC

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