About this opportunity
The Clinical Consultant is responsible for offering Treatment Planning Service (TPS) so as to guide doctors on ClinCheck treatment plan set up and explain about it with expertise. This role is to build Invisalign providers’ clinical confidence and competencies by demonstrating the clinical application through giving guidance and support to doctors’ own cases.
In this role, you will…
• Address any questions or concerns of the Customers related to the features and applicability of ClinCheck software and ClinCheck treatment plans as provided on the Invisalign Doctor Site (IDS).
• Assist Customers with new functions related to ClinCheck including the latest ClinCheck software, and any other update or new release of the foregoing Invisalign treatment planning software from time to time and other associated services.
• Assist Customers to assess case and provide guidance on case suitability.
• Review and advise on ClinCheck plan to have a more predictable set up
• Be a core member of projects for treatment planning, clinical support model projects or any other projects that require product or clinical input.
• Engage and influence cross-functional teams to deliver an excellent clinical customer experience for all Invisalign providers.
• Drive efficiency and effectiveness through all Clinical processes.
• Participate in proactive team efforts to achieve departmental and company goals where applicable
• Comply with all safety policies, practices and procedures. Report all unsafe activities to manager and/or Human Resources
• Adhere to all company policies, procedures and business ethics codes and ensure that they are communicated and implemented within the team
• Other duties as assigned from time to time
In this role, you’ll need …
• Graduate of Doctor of Dental University, Bachelor Dental school (Must have)
• With Invisalign patient treatment planning and management at clinic or working in a corporate environment would be a plus.
• At least 2 years of Invisalign patient treatment planning and management at clinic
• Good technical knowledge and experience in dental
• Experience in training dentists/orthodontists
• Proficient in English
• Effective communication and presentation skill
• Regular business hours. Some outside hours in evenings and weekends, and travelling may be required from time to time
Job Responsibilities:
Essential duties include but are not limited to the following:
Deliver Results
• Achievement of Monthly, Quarterly and Annual Sales Targets, Operational Plan and Profitability Plan for Taiwan.
• Responsible for the working with assigned accounts and team within the organisation, including direction, motivation and development of sales plans, targets, and strategies and the removal of obstacles to success.
• Provide all appropriate reporting to Manager including feedback from customers on a weekly and monthly report
• Responsible for the sales area as ‘their business’ and be willing to take responsibility for its planning and development in what is a high growth business.
• Work closely with co-colleagues to develop a high-performance team in Taiwan.
Drive the Best Outcomes
• Acquire and maintain detailed knowledge of the company's products;
• Provide training in product knowledge, selling skills, and territory management, and Align Terms and Conditions of Business
• Co-operation with co-colleagues through observation during co-travel, frequent feedback and the analysis of data
• Evaluate levels of customer, product and systems knowledge via in-field assessment
• Provide appropriate training and field coaching as required.
• Build strong ethical business relationships with customers to ensure usage of our products and gain greater market share by focusing high value activity and selling,
• Ensure professional dress code and attitude is maintained at all
• Participate in proactive team efforts to achieve departmental, company goals and comply with all policies, practices and procedures.
• Work with the Manager to set Operational plan for future periods and perform other duties as assigned.
• Keep abreast of what competitors are doing; and update Marketing Manager of market intelligence and pulses in the market.
• Be responsible for all quality updates records and customer product feedback for Taiwan market.
• Perform other duties as assigned
Lock in Key Relationships
• Engage certified doctors and develop potential for new cases; engage non-certified doctors and establish their potential as an Invisalign provider and current submitters to develop Invisalign business
• Balance the short term operational needs with the long term organizational needs of the business
• Work closely with Marketing Manager to develop and implement sales and marketing strategies; such as management of Platinum Elite Accounts as well as opening new accounts and assist customers to achieve sales, distribution and display objectives.
Learn more about the role:
https://video.digi-me.com/align-technolog/jobs/marketing-sales/global-field-sales/jv_Align-Technolog_3
We are seeking a Clinical Operations Coordinator to oversee the planning and execution of clinical studies in compliance with GCP/ICH guidelines and company SOPs. This role serves as the primary contact for clinical trial operations and manages day-to-day activities to ensure successful study completion.
1.. Study Oversight & Compliance
- Lead planning, execution, and management of clinical studies.
- Ensure compliance with GCP/ICH guidelines, applicable regulations, and company SOPs.
- Act as the primary point of contact for all clinical trial operational activities.
2.. Team Leadership & Coordination
- Manage day-to-day activities of the clinical operations team.
- Provide guidance and oversight to ensure timelines, budgets, resources, and quality standards are met.
3.. Cross-Functional Collaboration
- Work closely with clinical project managers, medical monitors, pharmacokinetics, data management, regulatory affairs, and pharmacovigilance teams.
- Ensure efficient and effective study conduct through cross-functional alignment.
4.. Stakeholder Communication
- Communicate study progress to internal and external stakeholders.
- Identify and mitigate study risks and issues proactively.
5.. Site & Vendor Management
- Oversee investigational sites and third-party vendors to ensure high-quality execution.
6.. Documentation & Systems
- Ensure clinical project-related documents and systems are developed and maintained to high standards.
We are seeking a highly skilled Website & Digital Content Specialist to join our pharmaceutical company in Taiwan. This role will be responsible for managing, updating, and optimizing our global website content, ensuring accuracy, compliance, and timely execution of updates. The ideal candidate will have strong experience in biopharma or life sciences content management, excellent English proficiency, and the ability to serve as a key liaison with cross-functional teams, including our U.S. headquarters, medical/legal/regulatory (MLR) review boards, and brand planning committees.
This position goes beyond execution: the selected candidate will also contribute strategic insights on how to improve website engagement, align digital content with brand strategy, and enhance our global online presence.
<Key Responsibilities>
1.Website Content Management
• Own the process of updating and maintaining company website content (corporate, product, medical education, and brand-related pages).
• Ensure scientific and medical accuracy of all published content, with special attention to regulatory compliance.
• Coordinate urgent or time-sensitive content updates, ensuring flawless execution under tight timelines.
2.Cross-Functional Collaboration
• Act as the key owner and liaison for Medical-Legal-Regulatory (MLR) review processes, ensuring all digital content passes required approvals.
• Work closely with U.S. and Asia-based teams, bridging time zones and cultural contexts to ensure seamless communication.
• Participate in brand planning discussions, contributing recommendations on content strategy and alignment with brand goals.
3. Digital Strategy & Social Media
• Support and enhance the company’s digital presence across owned media (website, social media, corporate communications).
• Leverage social media management experience to recommend content strategies and community engagement initiatives.
• Monitor digital content performance and propose optimization opportunities.
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.
【Job Description / Capsule】
WHAT YOU WILL DO:
- Collaborate closely with Marketing team in Oncology Business Unit to develop and execute campaign strategies and marketing collateral.
- Support to manage the end-to-end campaign lifecycle, including content creation, approval workflows, execution monitoring, performance tracking, and data-driven analysis.
- Serve as a liaison for internal teams and external vendors, ensuring clear and timely communication.
- Provide logistical support for Marketing events, coordinating all associated operational details.
- Oversee alliance coordination activities and maintain accurate data records.
- Organize and facilitate internal meetings to support Marketing initiatives.
Anne Yao
Direct:02-7720-5802
Email:anne.yao@adecco.com
CRA for BE study/New drugs/Medical devices
1.Clinical research study setup/study procedure setup/site staff training
2.Site monitoring visits/source data verification/deviation reporting in compliance with GCP
3.Trial documents maintenance/regular site visits and maintenance/study materials supply/interim reports
4.regular report to sponsor/communication between sponsor and site.
5.site close-out/trial materials retrieval
6.audits/regulatory inspection participation upon request