Clinical Pharmacologist

Job Title

Resonsible China Clinical Pharmacology strategy (including intensive PK, popPK, PK/PD, E-R, Immunogencitiy and QT analysis) to ensure: 1) smooth opening of late phase study in China; 2) relevant China CP regulation is fullfilled for a successful NDA registration

Serves as the clinical pharmacology representative in assigned China ASTs/IEST and TARM meetings

Serves as the (China) clinical pharmacology representative in assigned (global) study teams, to faciliate study execution

Work closely with related asset global Clin Pharm representatives in timely exchanging the relevant information and provide advise/input from the Chinese regulatory and scientific perspectives to support asset China CP strategy and study execution

Serves as the subject of expert of CP in China with close connection with global CP for professional support and collaboration

A critical reviewer and contributor for China CP documents for CTA and NDA submission, such as China PK study protocol/report/summary, related population PK report, exposure/response analysis report etc.

A key contributor/reviewer for CP part of local CDE consultation related documents (e.g. briefing book, CDE response letter), and CP part of CTA and NDA submission document (e.g. China specific clinical overview, IB and CTD, dose justification, study design justfication/China development plan).

Participate in local CDE consultation meetings and facilitate CP related communication with regulatory agency

Scienfcally interpret CDE's CP requirement in e.g. pre-CTA response, CTA letter, query/deficiency letter during NDA (working together with RA, CPPM and CD), ensure CDE's requirement is implemented/fulfilled to derisk for regulatory activities.

Mangement of local KOLs

Manage related communications and collaborations between China AST and global AST/IEST in collaboration with the global CP counterparts

Qualifications

Master or above degree in pharmacy, pharmacology, biology, medicine or related area, with Ph.D. preferred

0 year or more experience in clinical pharmacology in industry with PhD, 4-year or more experience in clinical pharmacology in industry with Master degree.

Good interpersonal skills, and ability to effectively interact with internal and external stake holders

Knowledge of strategic thinking

High proficiency in written and spoken English communication skills

Experience of working in MNCs is preferred

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

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Pay Range: $-

Where We Work

Role is primarily site- or office-based but can occasionally be performed remotely. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.