Biomarker Science Liaison-Hefei

Job description

Biomarker Science Liaison-Hefei

Your Role:

•Build strong relationships with pathologists and technicians in the area of​​biomarkers at national and regional levels

•Responsible for organizing, leading and developing projects and action plans arising from the strategy of biomarkers (eg training, quality control, local meetings, events, conferences etc)

•Identify needs and market opportunities in the area of​​biomarkers, developing specific actions that impact on an improvement in the quality of diagnosis and is related to the use of targeted therapies.

•Support the development and implementation of clinical trials (Biomarker & Drug) in accordance with the Medical Advisor and the respective product strategy and Biomarkers.

•Ensure adequate communication and coordination with pathologists, technicians and oncologists and be involved in the targeted therapy related diagnosis and treatment that are perfectly aligned.

•Contribute and participate in the development of the strategy and action plans Biomarkers unit.

•Regular updating of actions and projects

•Responsibility for the budget assigned, ensuring maximum return on investment

•Monitoring and control of the budget allocated to product, meeting the dates for the rolling forecast.

•Conduct training on biomarkers to other functions of the organization

•Head of biomarkers in their area, leading the strategy, coordination, implementation and monitoring of specific action plans.

•Coordination and communication with the sales in accordance with company policies on biomarker strategy and actions.

•Responsibility for target and resources assigned, ensuring maximum quality outcome.

 

Who you are

    Master or Diploma of Science preferred

    Excellent knowledge of English

    Proven experience as Clinical Data Manager in the pharmaceutical/biotechnology industry, equivalent to 6 - 8 years

    Successful completion of multiple studies from beginning to end providing a full scope of DM experience

    Experience to supervise surveillance of CRO activities regarding the quality and timeliness of the deliverables and ensure the database is ready for lock

    Proficiency with data management systems such as ClinTrial™, InForm™

    Basic knowledge of SQL is a plus

    Good knowledge of SAS

    Understanding of relational database design

    Proficient Computer Skills e.g. word processing, spreadsheets

    Knowledge of medical terminology required

    Excellent knowledge of regulations and guidances with regard to clinical development and the systems used in this context

    Excellent written and verbal communication skills

    Excellent organization skills

    Individual must be detail oriented and have strong prioritization skills

    Excellence in planning and self coordination

    Ability to handle multiple projects

    Problem solver with consensus building skills, critical thinker

    Leadership skills and team player

    Proven leadership and project management skills and experience

    Mentoring and training skills

 

HR95601

Functional area: Regulatory & Medical affairs

职位需求编号: 197021

位置: 合肥

职业阶段: C - 工作年限（1 - 3年）

工作时间模型: 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.

职位细分: Oncology, Pathology, Biotech, Medical, Developer, Healthcare, Science, Technology