Local Trial Manager(oncology)-BJ
职位描述
职位描述:
Responsibilities
1. Responsible for customizing the Master Clinical Trial Agreement (mCTA) including site / vendor and study specific information;
2. Responsible for analyzing contract requests/needs and translating into appropriate contracts/budgets for company sponsored clinical trial agreements;
3. Lead negotiation of third party contracts and budgets, ensuring the budget meets HCC/HCBI requirements (including budget verification with fair-market value) and contract contains appropriate wording for the third party
4. Acts as primary local/country contact for clinical trial agreements and site specific (budget) templates with clinical trial sites. In case of legal matters, act as liaison between the local study site , Local Trial Manager and the (local) legal department;
5. Calculate study budget based on results of negotiations with third parties;
6. Keep cross-trial and cross-site oversight to create consistency and ensure accumulated learning and updated records from each negotiation round;
7. Create local budget overviews with LTM support;
8. Evaluate potential needs for contract amendments and manage amendment lifecycle; ensuring that contract amendments are appropriately executed;
9. Work with the global C&G, HCC&P,legal affairs, finance teams and GCO Q&C as necessary to review and analyze contractual terms and conditions in order to reach acceptable language. Act as liaison in risks assessment of budget and legal provisions in conjunction with members of the C&G team and support functions and communicate such to stakeholders. Liaise with C&G management, Healthcare Compliance, Risk Management, Privacy and other stakeholders to obtain guidance and escalate issues as appropriate.
10. Work proactively to improve processes and establish refinements that reduce cycle time, create savings and improve efficiency in the initiation of clinical trials and activation of clinical trial sites.
11. Comply with requests from QA and auditors.
12. Responsible for managing the mCTA data oversight: provide qualitative and quantitative input into any revisions of the mCTA and maintain metrics on %adherence to mCTA standards, time to contract sign off to inform strategic discussions with the Research networks
13. Establish and maintain excellent working relationships and networking with external stakeholders, in particular hospital administration and contracting and internal stakeholders, including but not limited by Legal Affairs, Health Care Compliance and global C&G
14. Actively contributes to budgeting, contracting and payment to third party process improvement;
15. May represent functional area in internal and external contracting initiatives
Requirements
University degree or other relevant tertiary education, with relevant working experience and affinity with the legal domain
Minimum of (2 to 6) years of pharmaceutical and/or clinical trial experience is preferred, however, other relevant experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility.
Solid understanding of the drug development process including ICH/GCP and local regulatory requirements. Must have a working knowledge of the clinical development process with 2 years of negotiation and contract experience
Familiarity with healthcare compliance and other relevant guidance (HIPAA, FCPA, Safe Harbor, Sarbanes-Oxley,etc.)
Ability to work effectively in cross function teams and able to influence individuals at all levels within multiple organisations;
Ability to negotiate over conflicting issues and develop win-win outcomes
Previous experience working in virtual teams preferred
Must demonstrate innovative spirit, have strong interpersonal skills, and ability to accomplish substantial tasks with minimal supervision
Computer literacy – advanced computer skills and detailed knowledge of a variety of software packages (Microsoft applications like Excel, PowerPoint, and Word …). Able to use a range of computer based systems (e.g. CTMS, internet applications, SharePoint) to track and monitor trial and investigational site-related activities.
Excellent communication, negotiation, networking and interpersonal skills. Proficient in speaking and writing the country language and English. Proven track record in contract negotiation and problem resolution.
企业简介
美国强生公司创建于1886年,目前在全球60个国家建立了250多家分公司,是目前世界上最具综合性、业务分布范围最广的卫生保健产品的制造商和相关服务提供商,业务领域主要包括制药,医疗器械和消费品。
西安杨森制药有限公司是美国强生公司在华最大的子公司,成立于1985年。公司管理中心在北京,生产基地位于西安,在全国28个城市设有办事处,在华员工超过3000人。在过去的25年中,西安杨森保持持续稳定发展,成为了中国领先的合资制药企业。
西安杨森不断引进和生产多种创新的、高品质的药品,其产品包括多种高质量的处方药,以及广受患者信赖的非处方药物。西安杨森依托强生公司全球强大的研究开发体系,着眼于未来,不断引进新的药品,计划上市生物制剂、肿瘤、心血管、风湿和泌尿等更多领域的产品以服务于中国的广大患者。
西安杨森公司遵从强生信条的原则,致力于公司的长期发展。这是公司在过去取得成功的基石,也是未来成长的保障。
西安杨森公司获得众多奖项和赞誉,比如《财富》杂志评选的“中国最受赞赏的外资企业”及“人力资源经理眼中的热门雇主”;中国中央电视台 “2005CCTV中国年度雇主”;CRF评选的2007-2008年度北京地区“中国杰出雇主”;2008年与强生在华公司一起荣获“第六届中国大学生最佳雇主奖和进步飞速奖”称号,和2009年“第七届中国大学生最佳雇主奖”,并位列医药行业第一名。2010年强生在华公司荣获“第八届中国大学生最佳雇主制药/医疗行业最佳雇主第一名”。这是继上届强生公司获得医药行业第一名后再次蝉联这项荣誉。
北京相关职位: 医药信息代表(儿童肥胖DSM)
热门区域招聘: 重庆 北京 上海 浙江 江苏 广东 山东 湖南 安徽 河北
北京招聘企业: 叮当智慧药房(北京)有限公司 北京久峰润达生物技术有限公司 北京协和医院 北京海斯美医药技术有限公司 北京策知易咨询有限公司 北京万泰生物药业有限公司 百济神州 北京凯霖娜国际贸易有限公司好益生医院分公司 中国生物制药有限公司 国药集团工业有限公司
职位发布日期: 2016-11-23