Life Sciences Job at ICON, Taiwan | Apply Online
If you are an experienced clinical research coordinator, a trial document specialist, or a life sciences professional looking to transition your site readiness skills into a global Contract Research Organization (CRO), this hybrid opportunity at ICON plc is an exceptional choice. Located at our regional office in Taipei, Taiwan, this position places you at the operational forefront of international regulatory submissions, ethics committee coordination, and clinical site activation. For organized data administrators tracking a competitive Life Sciences Job, this role (Study Start Up Associate I/II / Site Specialist I/II) offers direct ownership over regional trial milestones, investigator documentation networks, and essential document quality control. It serves as an elite corporate platform to advance an exceptional ICON Career and stands out as a premier selection for individuals looking to lock in a high-trajectory Life Sciences Job in Taiwan within a world-leading clinical research infrastructure.
About The Company
ICON plc is a world-leading healthcare intelligence and global Contract Research Organization (CRO) dedicated to delivering end-to-end clinical development services. Partnering with elite global pharmaceutical, biotechnology, and medical device innovators, ICON manages multi-center clinical trials across the globe, driving the underlying medical data, regulatory submissions, and clinical logistics required to bring next-generation therapeutics to market safely. The dynamic corporate office in Taipei, Taiwan, serves as a critical strategic node for East Asian clinical development. Joining the Study Start Up division embeds you within an agile, high-performance network that handles strict international protocols. Within this structure, your daily site-level document collection and milestone tracking serve as the primary defensive line ensuring that clinical trial pipelines remain uncompromised, structurally transparent, and continuously audit-ready.
Life Sciences Job – Key Responsibilities
The Study Start Up Associate functions as a vital central anchor for study teams and field monitors, taking primary operational responsibility for site readiness trackers, investigator communication networks, and administrative submissions steps.
Your core site tracking, document control, and coordination duties include:
- Dossier Collection & Review: Coordinating site-level essential document collection, review, and maintenance, ensuring complete accuracy and full compliance for assigned research sites or protocols.
- Operational Site Liaison: Acting as the primary operational liaison for site staff, principal investigators, and coordinators regarding documentation, systems access, and process-related questions to advance this Life Sciences Job.
- CTMS Database Administration: Maintaining up-to-date site activation status, metrics, and key milestones in internal clinical trial management tools to ensure data transparency.
- Logistics & Meeting Coordination: Supporting planning and logistics for investigator meetings, site initiation meetings, and baseline clinical monitoring visits.
- Process Improvement Contribution: Identifying operational opportunities to streamline site onboarding workflows and contributing directly to regional process improvement initiatives.
- Peer Mentorship & Guidance (Level II): Providing structured guidance, operational onboarding, and technical support to Site Specialist I or junior colleagues, sharing best practices to support their professional ICON Career progression.
Qualifications & Profile Requirements For Life Sciences Job
ICON seeks a systematic, detail-oriented team player who demonstrates excellent time management habits and a service-focused approach to site support.
- Required Academic & Experience Criteria:
- Educational Foundation: A completed formal Bachelor’s degree in the Life Sciences or a related field (or equivalent clinical research experience) to anchor your track for this Life Sciences Job in Taiwan.
- Professional Background: Relevant experience in site support, clinical trial administration, study start-up, or similar roles within a CRO, pharmaceutical corporation, or hospital healthcare environment.
- Good baseline understanding of clinical trial processes, Good Clinical Practice (GCP) guidelines, and localized site documentation requirements.
- Core Skills & Competencies:
- Strong organizational and problem-solving skills, with the proven capability to manage multiple research sites and changing project priorities simultaneously.
- Excellent written and verbal communication traits, with a proactive, service-focused mindset when interfacing with hospital personnel.
- High comfort level working independently in a virtual workspace while collaborating effectively with international, cross-functional teams.
- Proficient computer literacy, featuring a solid working knowledge of Microsoft Office applications and comfort working with electronic databases.
In short, the Study Start Up Associate position at ICON plc is a definitive route to translating your clinical coordination or trial administration background into a premium asset within global clinical trial management. Securing an appointment here allows you to bypass general laboratory testing loops and take direct, hybrid operational charge of the CTMS data fields, site activation dossiers, and regulatory documents that activate clinical trials safely. If you reside in Taipei, meet the bachelor’s science baseline, and possess an analytical, zero-error approach to tracking documents, apply today via the recruitment portal to secure this premier choice in a Life Sciences Job, accelerate an exceptional ICON Career, and lock in this outstanding Life Sciences Job in Taiwan.
