北京招聘

POSITION SUMMARY 

Responsible for preparing, negotiating, and finalizing agreements and budgets related to clinical trials.  Provide support to the clinical team in the pricing, planning, execution and control of site/investigator budgets and contracts.

RESPONSIBILITIES

？ Prepare, negotiate, and finalize clinical trial agreements and ancillary agreements for company sponsored and/or investigator initiated studies through direct negotiation with Clinical Trial Sites. Responsible for delivery against established targets/measurements.

？ Provide support for negotiations in confidentiality agreements, informed consent forms and other ancillary contract documents as required.

？ Participate in discussions related to the development of site/investigator budgets aligned with fair market value. 

？ Manage the contract amendment life cycle.

？ Work with the global C&G team as necessary to review and analyze contractual terms to reach resolution.  Assess risks of budget and legal provisions in conjunction with members of the C&G team and support functions.   Escalate issues as appropriate.

？ Work proactively to provide recommendations to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trial sites.

？ Assume responsibility for all aspects of legal document and metrics tracking.

？ Provide support to review, authorize and/or understand aspects of site payments.  Assist clinical operations or clinical team in ensuring that investigator grants comply with overall study costs and compliance guidelines.

？ Adhere to SOPs, ethics and departmental compliance as determined by departmental management as well as operating companies, corporate, HCC and QA guidelines.  Ensure familiarity with departmental and appropriate corporate processes.

？ Comply with requests from QA and auditors.

？ This is not an exhaustive, comprehensive listing of job functions. Other duties may be performed as assigned.

Requirements

？ 1- 3 years’ SSU experience and/or equivalent competencies in legal/pharmaceutical industry/clinical research

？ Excellent communication skills (both oral and written)

？ Familiarity with healthcare compliance and other relevant guidance 

？ Familiarity with clinical research processes

？ Ability to work effectively in cross function teams

？ Strong and proven negotiation and problem resolution skills

？ Working knowledge of PCs (MS Office suite at a minimum) and database management

？ Fluency in English is required

？ Must demonstrate innovative spirit, have strong interpersonal skills, and ability to manage a high volume of work

？ Previous experience working in virtual teams preferred

We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.