Jobs at Novotech

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.

Plan, coordinate and drive regulatory start-up activities for regional CRO projects. Develop RSU strategies and management plans, oversee submissions to authorities and ethics committees, manage site activation packages, track progress in CTMS, identify and mitigate start-up risks, liaise with clients and cross-functional teams, present at meetings, support bids, and recommend process improvements.

Lead global end-to-end executive recruitment (Director to C-suite), build in-house executive search capability, drive global TA strategic programs (operating model, governance, D&I), and partner with senior leaders and Finance on headcount planning and workforce governance.