- 3-4年经验
- 本科
- 招2人
- 02-22 发布
- 五险一金
- 补充医疗保险
- 通讯补贴
- 专业培训
- 年终奖金
- 弹性工作
- 定期体检
职位描述
SUMMARY: Reviews and analyses project specific data and medical literature. Manages study-related committees such as Data Monitoring Committees (DMCs), Data Safety Monitoring Boards (DSMBs), and Adjudication Committees. ESSENTIAL FUNCTIONS: Performs review of medical data listings, Case Report Form (CRF) line and lab listings, and medical coding; highlights areas for medical review.Performs analysis to identify trends within data, line, and lab listings.Performs initial assessments for Medical Affairs Pre-Enrollment Review process. Assists Medical Monitor(s) with creation of Medical Management Plans.Creates project plans related to Medical Data Review, Endpoint Management, and Pre-Enrollment Review. Primary interface between Company and sponsors, vendors, and other departments in the area of DMC, DSMB, Safety Committee and Adjudication Committee management. Provides specialized knowledge for international guidance regarding the conduct of study-related committees.Uploads and manages documents collected for pre-enrollment review and endpoint adjudication into TrialEASTM. OTHER RESPONSIBILITIES:Performs other work related duties as assigned. Minimal travel may be required (up to 25%). REQUIREMENTS: BA/BS in the biological sciences or related discipline in the natural sciences/health care field, nursing degree, or equivalent combination of education and experience. MS in a Healthcare, Business Administration, Public Administration, Public Health, or equivalent degree preferred. Moderate clinical research experience and management experience. Experience in a Clinical Research Organization and related therapeutic specialties preferred. Knowledge of financial budgets and various financial analysis tools. Superior proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, MS Project), email, and internet. Strong presentation skills, interpersonal skills, as well as a team oriented approach. Excellent verbal, written, and communication skills. Ability to multitask under tight deadlines while providing attention to detail and high quality work. Ability to be flexible, adapt to change, work independently, as well as work in a matrix environment. 职能类别: 其他
联系方式
国贸
公司信息
InVentiv Health通过分布在全球70多个国家的14000名员工,为医药、医疗器械和生物工程客户提供临床研发、销售及商务咨询服务,inVentiv Health的目标是通过自身的专业服务将客户的商业理念真正地转化为现实,帮助客户提升业绩,现在inVentiv Health服务于约550家客户的850个品牌。 2011年12月,inVentiv Health在中国设立盈帆达医药咨询(上海)有限公司,正式在中国区域为医药行业客户提供服务。 inVentiv Health Clinical, formerly PharmaNet/i3, is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 7,000 employees in more than 36 countries, inVentiv Health Clinical offers therapeutically specialized capabilities for all phases of clinical development, bio-analytical services, and strategic resourcing from a single clinical professional to an entire functional team.
北京相关职位
-
临床协调员CRC 工作地点 广州 4-6千/月
-
高薪聘医疗器械销售 0.3-1万/月
-
技术高级经理 10-20万/年
-
临床协调员/CRC/临床试验/临床研究员/研究护士/SMO 3.5-7千/月
-
临床协调员/CRC/临床试验/临床研究员/研究护士/SMO 3.5-7千/月
-
临床协调员/CRC/临床试验/临床研究员/研究护士/SMO 3.5-7千/月
-
临床协调员/CRC/临床试验/临床研究员/研究护士/SMO 3.5-7千/月
-
CRA Trainee(面向CRC/CTA)J10239 6-8千/月
-
CRA Trainee(面向CRC/CTA)J10242 6-8千/月
-
质量主管 6-8千/月
-
质量主管 6-8千/月
-
销售代表 4.5-6千/月
-
试剂研发技术人员 3-4.5千/月