新加坡商安健醫療器材國際有限公司台灣分公司

本公司主要產品為治療心臟血管相關疾病之耗材(心臟&周邊血管塗藥球囊DEB、一般球囊Balloon)。 工作範圍為各大教學醫院、區域醫院心臟內、外科及心導管室。 工作內容： 1。顧客服務及維繫。 2。協助訂單處理、送貨、交發票。 3。各區定期盤點。 4。行政文書、主管交辦事項.....等。 ※歡迎應屆畢業生。 ※有對帳經驗者佳。

本公司主要產品為治療心臟血管相關疾病之耗材。（周邊&心臟擴張球囊、塗藥氣球、塗藥支架） 業務工作為拜訪教學醫院、區域醫院心臟內科及相關臨床與行政單位。 1.開發或維護客戶關係。 2.銷售及推廣公司產品。 3.教育及示範產品使用方式。 4.協助客戶使用產品。 5. 配合行銷活動並隨時更新客戶以及市場競爭資訊。 6. 工作地點：南部地區依公司規定分派

本公司主要產品為治療心臟血管相關疾病之耗材。（周邊&心臟擴張球囊、塗藥氣球、塗藥支架） 業務工作為拜訪教學醫院、區域醫院心臟內科及相關臨床與行政單位。 1.開發或維護客戶關係。 2.銷售及推廣公司產品。 3.教育及示範產品使用方式。 4.協助客戶使用產品。 5. 配合行銷活動並隨時更新客戶以及市場競爭資訊。 6. 工作地點：中部地區依公司規定分派

本公司主要產品為治療心臟血管相關疾病之耗材。（周邊&心臟擴張球囊、塗藥氣球、塗藥支架） 業務工作為拜訪教學醫院、區域醫院心臟內科及相關臨床與行政單位。 1.開發或維護客戶關係。 2.銷售及推廣公司產品。 3.教育及示範產品使用方式。 4.協助客戶使用產品。 5. 配合行銷活動並隨時更新客戶以及市場競爭資訊。 6. 工作地點：北北基地區依公司規定分派

SynergAsia Health Pte Ltd is a new Clinical Research Organisation focusing on clinical research in the medical device industry. We are looking for an organized Project Manager to implement and oversee projects, and to ensure quality of trials. The Project Manager outline project together with client and clinical monitoring team. The Project Manager regularly visits Clinical Trial Investigators, issues them supplies, such as Case Report Forms and Investigational Product. You will gather Case Report Forms and ascertain their quality, and collaborate with Clinical Trial Investigators to write final technical reports. To be successful in this role you need to ensure the project meets the client's goals within budget and on time. Top candidates are proficient multitaskers, client-oriented and have the ability to prioritize tasks. Project Manager Responsibilities: •Set targets for clinical monitoring staff, and ensuring recording of trial in compliance with project goals. •Creating and implementing study-specific clinical monitoring tools and documents. •Creating and overseeing trial budget. •Coordinating and supervising clinical monitoring team. •Providing Clinical Research Associates with project-specific training and having regular meetings with them. •Recording and sharing interactions with client, and acting as their representative. •Arranging and overseeing site visits. •Gathering and examining trial documents. •Assuring compliance SOPs and local regulations, and CFR, ICH and GCP guidelines.