深圳招聘

Key Accountabilities:

·       Playing the role in scientific leadership, including study design, literature reference research, project direction, and scientific discussion;

·       Interacting with clients to initiate and finalize outline protocols; Must be able to scientifically articulate the value of various pre-clinical models to clients

·       Taking full accountability on precise execution of the signed experimental protocol, submission of intermittent data to clients, resolution of operational schedule conflicts, documentation of modification/revisions to the study protocol, examination of data validity and analysis, interpretation of data, completion of study report, and collation and archive of study related materials according to company’s policies and client’s requests;  

·       Leading/mentoring, training, coaching and delegating all direct reports (study coordinators) on project and time management;

·       Ensuring adhesion of project timelines by proactive scheduling with managers of operational laboratories;  

·       Transferring technical skills and providing scientific literatures required in executing the animal models/procedures to operational staff and ensuring documentation of the transfer and the standard operation procedures;

·       Developing and integrating new models /assays and technology into current evaluation system;

·       Being responsible for contributing to the preparation and submission of invention disclosures, and patent applications, to secure intellectual property;

·       Writing technical reports or manuscripts to peer-reviewed journals;

·       Initiating and managing internal collaborative projects.

Requirements:

·       Ph.D. or M.D. with a specialty in pre-clinical in vivo toxicology/pharmacology research.

·       Strong background in in vivo pharmacology evaluations is critical. More than 1 year of work experience and the experience in biopharmaceutical industrial setting are preferred. Management and client communication skills are highly required.

·       Knowledge of the drug discovery process and role of pre-clinical disease models in supporting IND filings

·       Understanding of PK, PK-PD and target engagement assays in drug development,

·       Mature, open and team player.

·       High proficiency in both  written and spoken Chinese and English.

·       Good organizational and prioritization skills, and flexibility to adapt to changing priorities.

·       Excellent interpersonal skills, with the ability to be a team player.

·       Ability to communicate and apply concepts of recent R&D strategic scientific and operational initiatives.

                                                                                        

  

  

澎立是2008年成立的港澳台投资公司，提供一站式临床前药效学综合评价服务，即建立一套稳定的各领域动物疾病模型，测试客户候选药物的药效反应，以及医疗器械的生物适用性。服务的疾病领域包括炎症、自身免疫性疾病、肿瘤学、***疾病、代谢类疾病、骨代谢以及骨外科。非人灵长类动物疾病模型是为公司特色型服务代表之一。公司服务对象包括全球制药企业、生物科技单位及医疗器械公司等。公司建立的药效学综合评价服务平台，已在张江高科建成总面积为4300平方米的基地设施，其中包括1600平方米的普通级和SPF级动物房设施。成立后一年内，即先后获得美国实验动物管理认可协会(AAALAC)专业认证、上海市科委颁发的实验动物使用许可证和上海市病原微生物实验室BSL-2资质。公司内大小动物房、手术室均安装高清摄像机，数据信号经由实时影像系统，可为世界各地的合作客户实时监控。为规范实验数据管理，公司成为中国***家购买BioBook软件的CRO，所有原始数据直接录入数据库，无法篡改，达到美国FDA第11部分对于实验数据标准的要求。澎立的管理团队具有丰富的创业和外包服务运作经验，是国内药效学动物模型服务领域的领军人物。

澎立目前已建立起中国一流的药理学平台，立足于为国际国内药企提供国际水准的专业药理药效检测与评价服务，拥有世界领先的各类疾病动物模型、国内最出色的免疫药理平台和先进的人源化动物评价系统。