广州招聘

General Description The Clinical Research Manager will coordinate and manage clinical research projects according to appropriate quality standards and regulations. He or She will provide all clinical planning and study management to development projects according to established budget and timelines.
Roles & Responsibilities
Together with the Country Manager performs the following:
1. Project Planning – Create a project team, communicates final protocol and explains scientific approach/performance measures to the team (e.g., cost, time, quality).
2. Project Monitoring and Guiding - Monitors/evaluates/reviews the scientific performance of the study. Provides client with periodic updates including technical and time/cost issues.
3. Project Problem Management - Discusses study problems or scope changes with the client, suggests solutions and actions to solve study problems, manages the impact on time and cost, reviews protocol changes, and communicates the status of changes to client.
4. Learning Process - Performs scientific mentoring activities (e.g., training study specific techniques, assisting with complex analytical work/problem solving). Participates in post project assessment by providing input on team performance (accomplishments and glitches). Responsible for the design, conduct, and reporting of studies to meet scientific, regulatory, and client requirements.
5. Initiate a long-range planning and technical policies of the department.
6. Responsible for the planning and delivery of the clinical component of the project in accordance with the scope of work and contracted timelines, and for managing the clinical portion of the study budget.
7. Responsible in resource allocation, task oversight and delegation, development of monitoring plans, contingency planning, and management of client communications and reporting.
8. Lead in preparation and delivery of study documents for example SDV plan, study management plan for deliverables, confidentiality agreements and clinical trial applications.
9. Provide clinical monitoring expertise and leadership for large, complex protocols and/or international programs.
10. Lead and motivate the clinical team. Act as a mentor and train CRA in the responsibilities of the position.
11. Promote effective teamwork among project team members.
12. Key client contact for assigned projects.
13. Establish excellent working relationships with client project teams to ensure client satisfaction and operational excellence.

14. Provide performance evaluation and feedback of team members.
15. Work independently and to effectively prioritize tasks, actively seek input, problems solve and work within a matrix team environment.
16. Effective verbal and written communication skills. Highly effective interpersonal and organizational skills. Effective presentation skills, is able to prepare a presentation for an investigators meeting.
17. Coordinate operational aspects of study and lead and participate in activities that ensure quality, consistency, and integration of study data and progress deliverables to time cost and quality from study concept through database lock and study close-out activities.
18. Establish and maintain key interactions with major customers (internal/external) and interface with clinical departments (e.g. Biometrics) to ensure quality of study deliverables.
19. Provide input into non-project work, training activities, and development of procedures as needed.
20. Manage external service provider (Third Party Vendor)
21. Help in the development and implementation of plans associated with audits and regulatory inspections
22. Planning and conduct of Investigator/monitors meetings.
23. Manage/Coordinate the supply and reconciliation of Study Materials and Investigational product.
24. Demonstrate willingness to take on any level project activity consistent with current or past experience in support of study delivery.
25. Quality contact person of the department and in charge on the development and implementation of all HQ SOP and Local SOPs.
26. Assist the Country Manager with the staff recruitment.
27. Assist in business development in proposal generation and undertake feasibility work.
28. Provide monthly reporting to the Country Manager on the following
a. Project Status
b. KPI
c. Project Revenue
29. Perform other related duties as assigned.
Qualification
Physician, General Practitioner; or university biological sciences or science/engineering degree.

Experience
Minimum of 4 years of clinical research experience.

Skills
Demonstrated leadership and management skills.Excellent written and verbal communication skills.
Ability to solve problems, work in teams, present complex data, handle multiple tasks, and to understand and work with multiple different types of complex disease entities.
Knowledge of clinical trial design, analysis and reporting

Gleneagles Clinical Research Centre is a leading Pan-Asian Contract Research Organization (CRO), that caters to the unique needs of clinical research and drug development companies in their operations across the region. Gleneagles CRC has a network of over 50 hospitals sites for conducting clinical trials in Asia - Singapore, Malaysia, Indonesia, Thailand, Vietnam, the Philippines, Mainland China, Hong Kong, Taiwan, India, Australia and New Zealand.
Due to expansion and rapid growth, we are offering the following positions for suitably qualified and experienced individuals to manage our China business
Please send both English (compulsory) and Chinese CV. to us.

百汇鹰阁医药技术咨询有限公司隶属于新加坡百汇集团。新加坡百汇集团是亚太地区最大的私立医院系统，在新加坡拥有3家私立医院，包括鹰阁医院，伊丽莎白医院及东海岸医院，在海外还拥有8家医院的股份。百汇鹰阁医药技术咨询有限公司最初是为在百汇集团的医院进行临床研究服务，后来，由于我们高质量的服务，严格的GCP规范，在同行业中建立了良好的声誉，业务得到了迅速的发展，我们于2001年5月在北京建立了代表处，并于2002年1月正式在北京成立了分公司。
随着临床研究监查及统计项目的不断增多，百汇鹰阁在中国大陆已同数十个临床药理基地建立了紧密的联系，我们的临床研究涉及各个领域，在消化内科、内分泌科、肿瘤科、精神科、血液科、心血管科、中医学科等方面与多个专家建立了良好的合作关系。于30多家世界知名药企建立了伙伴关系。
请将中英文简历发送至指定邮箱，我们将根据公司的需要慎重考虑，如果您符合我公司的需要，我们将尽快通知您面试。一经录用将提供有竞争力的外企薪酬和相关的福利待遇。