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Associate Director Translational Medicine

Your role:


As a pivotal element of the strategic transformation of Global Development Translational Medicine presence in China R&D, this position will bring critical capacity to support multiple regional high-priority deliverables, build a network of outsourcing resources and strategic plans to capitalize on the growing regulatory and industry development opportunities. Provide scientific, operational, and strategic contribution to the growing China R&D portfolio of activities with focus in translational medicine, early development, clinical pharmacology, and experimental medicine related disciplines.


 

Key Responsibilities.
•Drive scientific excellence and contribute expertise to China programs◦Represent TxM in China Program/Project Teams.
◦Contribute to clinical protocol design, operation planning/logistics.
◦Participate in clinical report and regulatory dossier preparation/review.

•Lead early development activities to support China project deliverables◦Establish and maintain a robust and effective relationship with partner CROs.
◦Get involved in a broad spectrum of R&D value chain from non-clinical to clinical pharmacology.
◦Be responsible for quality aspects by supporting in- and external audit/inspection.

•Engage in China and pan-Asian R&D strategic discussion◦Seek opportunity for innovative early development pathways.
◦Bring integrated thinking and planning cross disciplines with other China R&D line functions.
◦Participate in joint China-Japan strategic planning.


 

Coorperation Scope.

Internally
•Global Development Translational Medicine, global functions Quantitative Pharmacology, Experimental Medicine/Clinical Biomarker & Diagnostics.
•All departments within R&D China Hub, including but not limited to,◦GCD (Global Clinical Development)
◦SBO (Strategic and Business Operation)
◦GRA (Global Regulatory Affairs)
◦GCO (Global Clinical Operation)
◦GMA (Global Medical Affairs)
◦GPS (Global Patient Safety)
◦GBEM (Global Biostatistics and Epidemiology, Medical Writing)
◦EI (External Innovation)


Externally
•Contract Research Organizations (CROs)
•Any external vendor relevant to the project
•Regional Health Authority (CFDA)

 

Who you are:

Required professional and technical training
•PhD or Master degree in pharmaceutical, biological or related field with 5-10 years of post-graduate experience in the life sciences industry.
•Excellent verbal and written communication skills in English.

Necessary professional experience
•Solid, hands-on knowledge of DMPK, toxicology, nonclinical, and clinical pharmacology.
•Experience working with a CRO or external partner.
•Good understanding of drug discovery and development process, working experience in GLP and/or GCP.
•Prior project management, project coordination, and/or contract and budget management experience.
•Familiar with regulations and guidelines from regional health authorities (e.g. NMPA).
•Experience working in global industry/academic setting with multi-cultural awareness.

Job Requisition ID:  190971
Location:  Beijing - all
Career Level:  D - Professional (4-9 years)
Working time model:  full-time

US Disclosure
The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law.  This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our HR Services team at 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday.


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