项目PM

面议

上海市

刷新时间：2021-04-26

职位描述

职位信息
o Responsible to work with the Business Development Department and/or Key Client Management Department to finalize the project budget and scope

o May act as a key contact for the Sponsor and Project(s) and establish and maintain good relationship with the Sponsor

o Lead, manage and communicate with multi-functional teams on regional or global interdisciplinary projects/studies to ensure on-time, and within budget deliverables for projects and be responsible for managing one or more projects concurrently

o May manage projects as Project Director or Project Manager to meet Company and Sponsor’s requirements and satisfaction. This includes managing resources, budgets, milestones, timeline and quality

o Plan, initiate, develop and organize clinical trials in accordance to the highest standards required in the good clinical practices, regulatory obligations, investigator integrity and compliance with study protocols and procedures

o Assess project resource requirements on a continual basis to ensure appropriate resources are allocated

o Work and coordinate directly with both pharmaceutical and biotechnology companies (collectively refers to sponsors) with overall responsibilities for managing the budget, timelines, qualities of all aspects of the assigned clinical trials/projects

o Work closely with sponsors to oversee the implementation of project specific procedures and requirements to ensure that the study goals and expectations (on-time, on-budget, quality performances) are met

o Resolve and recommend solutions and manage any deviation from plan or budget

o Set up, maintain, execute and implement project-related documents, dossiers and files, project databases, project timelines and processes, as well as tracking systems or other tracking/analysis tools for Sponsor and Management

o Review , finalize and approve all study-related regulatory and administrative documents (including investigator study budgets and contracts) from investigator sites, monthly client/site invoices, monthly monitoring reports, work progression reports and other documents

o Plan, coordinate and provide leadership in regular study team meetings and present at the Investigator’s meetings , site initiation meetings and/or site close-out meetings


Line Management

o Responsible to supervise and assess the performance of line staff whenever applicable, as well as motivate, train and develop line staff’s expertise to ensure efficient and effective day-to-day work tasks as well as to achieve targets

o Work with the Project Management Head to support business development activities or tasks as assigned by Business Development Department, Key Client Management and/or the Company

o Identify specific training needs and supervise, train and mentor project team/clinical research staff within the company on project related policies, procedures, project management tracking tools, and other relevant SOPs

o Measure and keep track team overall performance indices against projected baselines, timeline and milestones to ensure that all project work are completed and delivered to sponsor’s requirements and satisfactions

o Bachelor degree, major in nursing, pharmacy or other science-related background from a recognized institution, and/or equivalent combination of training and experience

o Minimum 6 years experience in clinical research, with at least 3 years prior experience in managing projects

o Advance knowledge of ICH-GCP guidelines, local GCP guidelines and regulations in the region

o Advance understanding of cross-functional processes, clinical trial processes and the regulatory environment

o Strong computer/technology skills including MS Word, MS Excel, PowerPoint, and MS Project (or similar Project Management tools)

o Effective written and verbal communication skills, preferably with good command of English in addition to local language

o Excellent organizational, leadership and interpersonal skills

o High integrity in personality and professionalism

o Ability to manage time and work independently

o Self-initiative to perform duties, with good analytical and problem-solving capabilities

o Ability to handle multiple tasks and expected to follow through with completion of assigned tasks with minimal supervision

o Meticulous and able to work in a fast-paced environment

o Able to work under pressure and under challenging timelines when required

o Ability to travel when required

o Possess strong sense of responsibility, dedication with strong work ethic and personal discipline

其他要求

招聘人数：1人
所属部门：临床部
汇报对象：总监
职能类别：临床项目经理PM

公司介绍

诗迈医药猎头是一家专业从事医药行业猎头服务的科技型企业，总部位于杭州，下属有上海、南京、广州、武汉等多家分公司，同时自主开发国内领先的猎头办公系统及医药人才网站，全面致力于海内外制药、生物、医疗、器械等行业线上线下人力资源整合。
公司与全国各地研发企业、生产企业及销售经营等企业及业内同行建立了良好互动平台，在欧、美、日等国家建立了海归引进平台，同时积极开展医药高等院校公益系列讲座，搭建了以人力、企业为主体的立体化咨询服务网，为医药企业人才队伍建设发挥了积极重要作用，为很多医药企业解决了高端人力之困。