• 3-4年经验
  • 博士
  • 招2人
  • 11-15 发布

职位描述

职位描述: Essential Functions:1. Playing the role in scientific leadership, including study design, literature reference research, project direction, and scientific discussion;2. Interacting with clients to initiate and finalize outline protocols;3. 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;4. Leading/mentoring, training, coaching and delegating all direct reports (study coordinators) on project and time management;5. Ensuring adhesion of project timelines by proactive scheduling with managers of operational laboratories;6. 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;7. Developing and integrating new models /assays and technology into current evaluation system;8. Being responsible for contributing to the preparation and submission of invention disclosures, and patent applications, to secure intellectual property;9. Writing technical reports or manuscripts to peer-reviewed journals;10. Initiating and managing internal collaborative projects.Requirements:1. Ph.D. or M.D. with a specialty in pre-clinical in vivo pharmacology research.2. Strong background in in vivo pharmacology models is critical. Minimum 3 years of work experience, preferably in the biopharmaceutical industrial setting.3. Ability to communicate and apply concepts of recent R&D strategic scientific and operational initiatives.4. Excellent oral and written communication skills, including ability to relate information concisely at a strategic level.5. Good organizational and prioritization skills, and flexibility to adapt to changing priorities.6. Excellent interpersonal skills, with the ability to be a team player.7. Very good skills in writing and speaking both in Chinese and English.8. 3 years experience in a CRO company is preferred. 职能类别: 医药技术研发管理人员 医药技术研发人员 关键字: 药效 药理

联系方式

上海市浦东新区张江高科技园区伽利略路388弄7号楼

公司信息

Phar***gacy Laboratories is a preclinical Contract Research Organization (CRO) providing specialty pharmacology services in Oncology, Bone, Inflammation, Immune Diseases, and Orthopaedics in Tissue Repairs and Tissue Engineering. The core business of Phar***gacy stems from our pioneering work and unique knowledge in developing and running specialized animal models to test drug candidates and medical devices for their pharmacological effects and biocompatible repairs, along with the adjacency studies of in vitro biology and PK/PD. Backed by a US private equity investment, Phar***gacy is strategically located in the heart of the Biotech and Pharmaceutical Base of Zhangjiang High Tech Industrial Park, Shanghai. We have a 45,000 square-ft facility with SPF labs. Our facility can house > 10,000 rodents and non-rodent animals. 澎立生物医药技术(上海)有限公司是一家临床前合约研究机构,致力于提供肿瘤学、骨骼、炎症、免疫性疾病领域的专业服务、以及与组织修复与组织工程相关的骨外科医疗服务。澎立生物医药的核心业务立足于公司的创新工作和独有的专业技能,研发服务涵盖专用动物模型的开发与运用、试用药物与医疗器械的药理效用和生物相容性测试、以及体外生物学与药代动力学(PK)和药效动力学(PD)的关联研究等。 澎立生物医药技术(上海)有限公司由美国投资,位于中国的生物产业‘硅谷’-上海张江高科技园区生物制药基地的中心区域。公司拥有占地45,000平方英尺的研发中心 ,其中包括大型SPF实验室和能容纳超过1万只啮齿类及非啮齿类动物的动物房。 公司邮箱 hr@phar***gacy.com

猎才二维码