Jobs at Novotech

Support start-up phase of clinical trials by preparing, submitting, and tracking country- and site-level ethics and regulatory authority applications per ICH-GCP and local requirements. Act as contact for sites, manage submission timelines, respond to reviewer queries, and advise project leads on local regulations to enable timely approvals.

Manage accounts receivable processes: prepare and post invoices, record customer payments (cash, check, wire), follow up on collections, resolve discrepancies, produce AR reports, review credit memos, and support process improvements to ensure timely, accurate payment recording and collections.

Prepare and manage proposals, budgets, RFIs and RFP responses for medium-complexity clinical research projects. Coordinate cross-functional inputs, assemble compliant proposal content, support contract drafting and negotiations, manage timelines and records, and escalate risks to ensure timely, accurate submissions.

Lead and scale the Global Shared Services finance function as 2IC to Head of Finance. Own end-to-end AP/AR/Billing/Banking/Expense/Balance Sheet operations, month-end close, reconciliations, payments, controls, and metrics. Drive process transformation, automation, M&A integrations, team leadership, stakeholder management, and deliverable quality across global locations.

Lead clinical systems, reporting and AI/automation initiatives for clinical operations. Manage end-to-end project delivery, stakeholder governance, KPI/reporting definition (Power BI/Excel), and drive adoption, compliance and process improvements across Veeva/Obvio and eClinical platforms.

The Clinical Research Associate manages relationships with site personnel to ensure clinical trials comply with regulatory standards and protect participant wellbeing, while overseeing site monitoring and data accuracy.

The Senior Pharmacovigilance Associate conducts PV-related work, supports system setup and updates, manages clinical project safety tasks, and prepares safety reports in compliance with regulations.

Prepare and manage submissions for IRB approvals, clinical trial agreements, site budgets, and training; monitor project status and ensure compliance.

The Inhouse Clinical Research Associate supports the clinical team's activities, manages documentation, ensures compliance, and assists with monitoring visits, specifically for clinical trials.

Support and maintain paper and electronic Trial Master Files (TMF) for assigned studies, perform comprehensive QC reviews, mentor/train junior DMAs, prepare reports, ensure TMF inspection readiness, support audits/closeout, and run TMF-related processes and documentation according to ICH GCP and SOPs.

Manage and monitor clinical trial sites in Taiwan to ensure GCP compliance, data quality, and patient safety. Conduct site visits, source data verification, trial documentation, and liaise with investigators and project teams to support study timelines and regulatory requirements.

Clinical Research Associate responsible for monitoring clinical trials, ensuring GCP and regulatory compliance, performing site visits, verifying data quality and source documents, and preparing monitoring reports to support study conduct and safety.

The Director Centralized Clinical Monitoring oversees Risk-Based Quality Management and centralized monitoring strategies, ensuring high-quality clinical trials and leading multidisciplinary teams.

The Senior Director of Quality Assurance leads the global Quality Management System, ensuring regulatory compliance, operational excellence, and quality strategy aligned with organizational goals. They oversee audits, support client engagements, and manage a high-performing QA team through budget and resource allocation.

The Clinical Research Associate manages site relationships, ensures compliance with ICH GCP and regulatory requirements, and verifies trial data accuracy in clinical studies.

The Inhouse Clinical Research Associate supports clinical teams, coordinates documentation, manages trial materials, and assists in preparing study submissions to ensure compliance with regulatory standards.

The Director leads the pharmacovigilance function, ensuring quality and financial targets are met while managing staff and cross-collaborating with various departments. Responsibilities include compliance with regulations, project management, staff development, and contributing to business development.

The Clinical Research Associate (CRA II/III) ensures trial participant safety and data accuracy, manages site relationships, and adheres to regulatory requirements.

The Project Manager oversees clinical projects from site selection to closeout, ensures compliance with regulations, manages risks, and maintains client relationships.

The Project Specialist assists the Project Manager in managing project deliverables, finances, timelines, and liaising with clinical teams for project success.