Jobs at Novotech

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 a distributed global commercial marketing team to drive pipeline, conversion, and revenue. Define global strategy, execute integrated campaigns (digital, ABM, content, events), develop performance dashboards, align marketing with sales and business development, mentor regional managers, and deliver metrics-driven optimization across regions to meet commercial targets.

Lead and scale Novotechs global brand and digital presence. Own brand strategy, creative direction, digital channels (social, SEO/SEM, web), marketing technology, analytics, and global team development. Drive marketing operations, governance, vendor relationships, AI adoption, and performance measurement across regions.

Lead global thought leadership strategy for Novotech, translating scientific and clinical insights into high-impact content. Manage SME relationships, develop editorial assets (white papers, POVs, webinars, conference content), direct agencies, measure performance, and align initiatives with brand and commercial goals while executing and managing cross-regional projects.

Lead multi-country clinical teams to deliver on-time, high-quality trial deliverables. Oversee site selection, monitoring, CMP/MVR development, CTMS oversight, recruitment strategies, data query resolution, safety reporting, TMF quality, and mentor CRAs while managing risks and stakeholder communications.

The Proposals Manager leads the proposal lifecycle, collaborates with teams to develop strategies, creates pricing models, and manages internal reviews for submissions.

Manage financial management and controls for assigned projects, support revenue recognition and forecasting, analyze realization and profitability, partner with Project Managers on budgets/forecasts, oversee month-end and project close-out activities, and ensure compliance with contracted project finance requirements.

The Inhouse Clinical Research Associate supports clinical team activities, manages study documentation, and ensures compliance with regulatory standards.

Manage site relationships and monitor clinical trial conduct to ensure participant safety and data integrity per ICH GCP, regulatory requirements, and sponsor/SOPs. Conduct site selection, initiation, monitoring and close-out (onsite or remote), support regulatory submissions, maintain TMF and clinical systems, drive recruitment, report visit findings, and assist project management for successful study execution.

The Clinical Research Associate (CRA) manages site relationships, ensures trial compliance, supports recruitment, and verifies trial data. They maintain documentation and facilitate regulatory submissions while monitoring site performance.

Manage and mentor a team of CRAs, SCRAs, CTAs and administrative staff to ensure clinical trials comply with GCP, SOPs and regulatory requirements. Oversee resourcing, performance management, training, site/vendor relationships, feasibility assessments, and support business development and country/office operations as needed.

Lead oversight of multiple early clinical projects and Project/Senior Project Managers, ensuring resource alignment, revenue recognition, change order governance, client account development, and project financial health. Establish account governance, engage senior client stakeholders, support CO negotiations and revenue recovery, collaborate with workforce planning for resourcing and succession, and provide line management, coaching, and performance management for S/PMs to secure phase pull-through and repeat business.

The Contracts Manager ensures accurate and compliant contract processing, collaborates with Sales and Legal, identifies risks, and drives operational excellence.

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

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

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