邢台招聘

Responsibility(工作职责)

• Medical Governance: To ensure Health Care Compliance on promotional material and Health Care Professional qualification in accordance with J&J policy, company GOP/SOP and related working procedure.
• To ensure the contents and medical claim in following parts of IFU, including Indication, contraindication, potential complications, clinical trial related contents, caution & precaution and adverse event, are accurate, fair and objective.
• MIR: To provide scientific and medical information to internal and external customers, including unsolicited requests from healthcare professionals, to ensure clinically appropriate and safe use of company products.
• Safety Vigilance: To work with other stakeholders as a team to ensure that all the information regarding Adverse Events in the field is collected to facilitate a correct and transparent communication of Adverse Events internally, and properly review the Adverse Events. Evaluate and submit the reportable Adverse Events to the competent Health Authorities in compliance with the company’s procedures and the local regulations. Keep good documentation on Adverse Event reported to the competent Health Authorities.
• To provide medical strategic plans and solutions to support business team on product and/or procedure management for related therapeutic area, in terms of evidence generation plan and proposal, evidence publication and dissemination, and other related activities.
• To collect investigators’ proposals (IIS) for local and regional clinical activities，to ensure that these proposals are discussed within the local clinical trial review committee, to coordinate Global Franchise approval processes, and to provide timely feedback to investigators. Coordinate and track the progress on contracting, project conduction and reporting after IIS approval.
• To develop and maintain professional relationship with external experts, in accordance with the company strategy to further understand and gain both insight and/or input into treatment patterns，including the scientific activities taking place within the disease area，and the needs and behaviors of healthcare professionals.
• To provide strategic medical support to the clinical research operation team on medical activities relating to the conduct of a trial or survey，e.g. protocol preparation, safety review, study report writing and publication. Maintain scientific contacts with local investigators.
• To partner with other functional stakeholders, to prepare Clinical Evaluation Report to support product registration.
• To develop an understanding SOPs and proper working instructions to ensure the internal process are in compliance with company policy and related regulation, if applicable.
• Other responsibilities defined in written procedures.（流程中规定的其它职责）

• At least master degree of Clinical Medicine.
• At least 4 years’ experience practicing medicine or products develop experience.
• Industry experience in pharmaceutical marketing, clinical operation, or medical affairs would be preferred.
• Good communicate skills in English, both orally and in writing.
• Having good co-operation abilities and a positive character.

Required Competencies 胜任能力要求 (Level 1- 4, see Appendix A)

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