Jobs at Novotech

The Associate Project Manager assists in managing multi-country clinical trials, ensuring compliance, vendor oversight, and client communications under the Project Manager's guidance.

Lead operational strategy for complex early phase trials (FIH, HV, SAD/MAD, adaptive designs). Develop integrated delivery models, scenario budgets, and risk mitigations; drive cross-functional alignment, prepare executive bid defenses, maintain audit-ready documentation, and mentor junior strategists to ensure scalable, high-quality early clinical development execution.

Lead and coordinate statistical programming across clinical studies: review protocols and SAPs, develop SDTM/ADaM specifications, program SDTMs/ADaMs/TFLs, ensure standards and regulatory compliance, mentor and supervise programmers, provide estimates and status updates, represent the company at client meetings, and contribute to process improvements and training.

The IT Analyst provides technical support within the IT service desk, resolves tickets, improves processes, and assists with IT projects.

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 the planning, execution, and management of clinical projects, ensuring timelines, budgets, and regulations are met. They act as the main contact between Novotech and clients, leading project deliverables and contributing to process improvements.

The Clinical Research Associate (CRA II/III) manages clinical trial activities, maintains communication with site personnel, ensures compliance with guidelines, and oversees participant recruitment and monitoring.

The Clinical Research Associate ensures trial participant rights and data integrity, manages site relationships, and oversees clinical trial compliance with regulations and guidelines.

The Director leads drug development consulting engagements, focusing on clinical pharmacology strategies, regulatory submissions, mentoring juniors, and business development in a collaborative life-sciences context.

The Clinical Research Associate is responsible for managing relationships with trial sites, ensuring data integrity, compliance with regulations, and supporting trial participant recruitment.