位于上海市, c23的 20 个优质clinical study management职位（正在招聘！）

In line with overall product strategy, the Medical Advisor is responsible for supporting the design, implementation and execution of Medical Affairs plans for assigned Therapy Area, providing scientific information, helping design & organise clinical studies, building educational dialogue with KOLs and regulatory stakeholders

About the Role

Major accountabilities:

Ensure medical enquiries are responded to in a high quality, timely manner, and in accordance with applicable standards; establish standard response documents as appropriate, for frequently asked questions.
Provide medical/scientific input into the development and execution of clinical trial or clinical research related activities, including initiation and oversight of clinical studies / clinical research within the respective therapeutic area.
Support country strategy for Non Interventional Studies/Investigator Initiated Trial activities.
Coordinate review and approval of medical materials and locally developed promotional materials; ensure medical materials provided from global or region for stakeholder engagement and events are tailored to local needs, and reviewed/approved per local/P3 guidelines.
Ensure medical insights are provided to cross functional groups, including, but not restricted to: Pharmacovigilance, Regulatory affairs, Market Access, QA, Commercial teams, Brand team and others.
Responsible for risk identification and assessment, mitigation planning as well as implementation and monitoring of appropriate internal controls within the area of responsibilities.
Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key performance indicators:

Works within Ethics & Compliance policies -Achievement of annual targets for medical activities

Minimum Requirements:
Work Experience:

Collaborating across boundaries.
Operations Management and Execution.
Project Management.

Skills:

Building Construction.
Clinical Practices.
Clinical Research.
Clinical Trials.
Drug Development.
Hazard Identification.
Health Sciences.
Immunology.
Intensive Care UnIT (Icu).
Internal Control.
Internal Medicine.
Job Description.
Medical Information.
Organization Skills.
Patient Care.
Stakeholder Engagement.
Tcp/Ip Protocols.
Utilization Management (Um).

Languages :

English.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

Division

International

Business Unit

Development

Location

China

Site

Shanghai (Shanghai)

Company / Legal Entity

CN06 (FCRS = CN006) Beijing Novartis Pharma Co., Ltd

Functional Area

Research & Development

Job Type

Full time

Employment Type

Regular

Shift Work

Accessibility and accommodation

Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

立即申请

完善您的搜索

在上海市, c23的clinical study management个职位

MSL Manager-IMMU

Meidical - Clinical Operation Manager - Shanghai

Sr.Compliance Manager

Principal Clinical Data Scientist II

Field Medical Lead - Immunology South, Medical, Shanghai

CRA (Level II)

FSP SCRA I(Changsha)

R&D Assistant

Director Clinical Supply Chain Operations

Operations Excellence Lead, Clinical Operations China

Regulatory Program Manager

Senior Direct GTM FSP APAC - Shanghai

Head of GCD China

Lead QA Specialist – New Product Implementation

Manager, Medical Affairs

Clinical Research Associate II/I

Feasibility Manager

Site Contracts Manager

Head of HGRAC and Operation Excellence

Therapeutic Area (Associate) Director

我想收到关于上海市, c23 的 clinical study management 的最新职位提醒

Related Searches

查看更多地区的职位

Summary

About the Role

Accessibility and accommodation

求职者工具

雇主工具

浏览

保持联系

完善您的搜索

在上海市, c23的clinical study management个职位

我想收到关于 上海市, c23 的 clinical study management 的最新职位提醒

Related Searches

查看更多地区的职位

Summary

About the Role

Accessibility and accommodation

我想收到关于上海市, c23 的 clinical study management 的最新职位提醒