1. Drive Sales Success: Achieve sales targets through the direct promotion of diagnostic equipment and reagents. Develop and implement sales strategies to optimize product mix and drive market share growth.
驅動銷售成功:通過推廣診斷設備和試劑,達成銷售目標。與部門主管共同討論並制定、執行銷售策略,以優化產品組合並推動市場佔有率的增長。
2. Engage and Influence: Proactively engage with potential customers, deliver persuasive sales presentations, and provide in-depth product demonstrations. Organize educational seminars for healthcare professionals and offer competitive pricing to meet customer needs.
擴張影響力:主動開發潛在客戶,提供具說服力的銷售簡報及深入的產品展示。為醫療檢驗專業人員組織研討會,並提供具有競爭力的價格以滿足客戶需求。
3. Track Performance: Continuously monitor sales performance against forecasts, contributing to market potential assessments and strategic planning for your assigned territory.
績效追蹤:持續監控銷售績效與預測進行對比,為市場潛力評估及區域的策略規劃做出貢獻。
4. Collaboration: Work closely with product specialists, customer service, and operations teams to deliver superior customer satisfaction and ensure seamless service throughout the sales cycle.
團隊合作:與產品專家、客戶服務及營運團隊緊密合作,提供卓越的客戶滿意度,確保銷售過程中的無縫服務。
**Preferred qualifications: Candidates with a background in Medical Technology, Laboratory Science, or related fields in Biology will be given priority consideration.
具醫學技術、檢驗科學或生物學相關科系背景者將被優先考量。
1. Drive Sales Success: Achieve sales targets through the direct promotion of NPWT, Collagen, and Dermal Matrix products. Develop and implement sales strategies to optimize product mix and exceed market share goals.
2. Engage and Influence: Proactively reach out to potential customers, deliver compelling sales presentations, and provide comprehensive product demonstrations. Organize educational seminars for hospitals and deliver competitive pricing tailored to customer needs.
3. Track Performance: Continuously monitor sales performance against forecasts, contributing to market potential assessments and strategic planning for the territory.
4. Collaborate for Customer Excellence: Partner with product specialists, customer service, and operations teams to deliver superior customer satisfaction and ensure seamless service.
驅動銷售成功:推廣負壓傷口治療(NPWT)、膠原蛋白和皮膚基質產品等產品來達成銷售目標。與區域業務經理共同討論並執行銷售策略,優化產品組合並超越市場佔有率目標。
擴張影響力:主動開發潛在客戶,提供專業的銷售簡報及全面的產品展示。為醫院組織教育研討會,並提供符合客戶需求的具有競爭力的價格方案。
績效追蹤:持續監控銷售績效與預測進行比較,為區域市場潛力評估及策略規劃提供支持。
團隊合作:與產品經理、客戶服務及營運等團隊間密切合作,提升客戶滿意度,並確保無縫的服務體驗。
1. Provide clinical and product service to customers
2. Responsible for sales target in assigned territory
3. Develop and execute sales plan to achieve sales target in assigned territory.
4. Build up customers' profile and ability to analyze customer data.
1. 推廣造口護理產品,教育及示範產品使用方式。
2. 拜訪、開發或維護客戶關係,並達成區域業績。
3. 規劃並執行區域計畫,達成區域目標。
4. 收集市場訊息,建立客戶資訊。
Brief Position Description:
The Site Management Associate (SMA) is responsible for planning, directing, and managing clinical trials at site. The SMA also implements remote site management activities according to the Site Management Plan, ensuring that clinical trials are conducted and documented, as per protocol, ICH GCP guidelines and applicable regulatory requirements and SOPs.
工作內容:
1. 協助醫師執行臨床試驗計畫
2. 完成資料及試驗數據之收集、記錄
3. 有研究護理師經驗者佳
4. 計畫及管理臨床試驗
5. 執行試驗場地管理 (依據試驗場地管理計畫)
6. 確保臨床試驗的執行及紀錄,是依據ICH GCP準則、本地及全球性的法規要求、諾佛葛及試驗場地的標準作業程序
Reporting to:
As indicated on current organisation chart.
Responsibilities:
Conduct and complete remote site management activities and/or on-site visits according to the Site Management Plan. Specific duties include:
Serve as a primary point of contact for site communication.
Implement study start-up activities including but not limited to gathering feasibility information, negotiation of contract and budgets, planning for subject recruitment, communication with IRB/IEC.
Collaborate with the principal investigator to prepare IRB/IEC and any other regulatory submission documents as required per protocol, ICH-GCP and local regulations.
Ensure amendments to an approved protocol, informed consent form, and other relevant documents are submitted to IRB/IEC for approval as required and assure that changes are not implemented prior to approval.
Arrange with monitor the scheduled date, time and location of site initiation visit. Prior to the site initiation visit, review the Investigator's Brochure and any up-to-date information on the investigational product for assessment of risk/benefit ratio of study participation in order to set Site Management Service Plan.
Perform study-related tasks delegated by the principal investigator within the contracted scope. SMA is responsible for performing tasks appropriate for its role, unless otherwise noted on a protocol specific delegation of authority log.
Support the investigator to identify suitable subjects for screening according to the eligibility criteria. If necessary, assist the principal investigator to use directed and IRB/IEC approved advertising (newspaper, TV, Internet advertisements, posters, etc.) materials.
Provide written and verbal site updates on study progress to the line manger according to the
study requirements/timelines. Ensure adequacy of information and data contained in site visit reports and other site management documents.
Manage the site expenses of clinical trial including but not limited to subject reimbursement,
material cost, travelling expense, cost for technical information, utilities and fees.
Main Responsibilities:
- Develop well thought out business plans and account profiles and execute sales and marketing strategies to achieve planned targeted revenue for those product lines responsible for.
- Develop business opportunities with new and existing clients to maintain product loyalty and increase market share. This includes identifying Key Opinion Leaders and building strong business relationships with these customers.
- Maintain close relationships with key accounts and ensure full customer satisfaction by providing appropriate Abbott products and services in response to the customer’s needs. This involves appraising customer needs and advising on product application or services.
- Provide clinical and technical support during case and inform the clinician of patient treatment options. Engage customers in meaningful clinical discussions, which can positively impact patient outcomes, while being presented in the procedure.
- Monitor territory sales performance on an ongoing basis, initiate corrective actions, and prepare reports, summaries, analysis and document an all aspects of territory management.
- Conduct product in-services, including physical demonstrations using non-sterile product and evaluation for successful account conversation.
- Strive to provide win-win outcomes for Abbott and customers while maintaining premium ASPs (annual sales prices) through leveraging of propriety products.
- Ensure all sales activities comply with legal and ethical standards, and that documented processes, procedures and internal quality management system are followed and adhered to.
- Initiate actions to prevent the occurrence of any non-conformities or customer complaints relating to the products, procedure and quality system.
- Assist in the development of lesser-experienced sales reps to extend skills sets and expertise of these individuals.
- Demonstrate a primary commitment to patient safety and product quality. Understand and comply with all regulations governing the quality systems for which I have executive responsibility.
- Commit to patient safety and product quality. Understand and comply with all other regulations governing their work.
- Attend all Quality related trainings and fully complied with SOPs including Traceability, PER (Product Experience Reporting)/Vigilance, Field Corrective Actions, Consignment Stock Management (where applicable), Customer Feedback Report.
We are seeking a drug development professional to join TaiMed's Clinical Development & Regulatory Affairs team.
Play a key role in advancing innovative therapies through clinical development and regulatory pathways.
- Coordinate global regulatory submissions (IND, BLA, and other CTD dossiers).
- Support GMP-related change controls to ensure regulatory compliance.
- Ensure efficient project execution with CROs.
- Coordinating communication among internal teams and external partners, many of whom are international. **Strong English communication skills REQUIRED **
- Study scientific literature, clinical guidelines, and global regulatory requirements for drug development.
- Title depends on experience.