Jobs at Novotech

Reviews, redlines, processes, and executes customer contracts, amendments, renewals, and related documents. Ensures compliance with approved templates, policies, approval workflows, and fallback positions while identifying and escalating risks. Manages contract data and documentation in CLM and CRM systems, meets processing SLAs, improves workflows, and collaborates with Sales, Legal, Finance, and Operations to support deal velocity and accurate, audit-ready execution.

Reviews, redlines, processes, and executes commercial contracts, amendments, renewals, and related documents. Applies contract policies and approval workflows, identifies risks and non-standard terms, and escalates issues appropriately. Manages contract data and documentation in CLM and CRM systems, meets processing SLAs, supports process improvements, and collaborates with Sales, Legal, Finance, and Operations to accelerate deal execution.

Develop operational strategies for clinical trial proposals across non-oncology therapeutic areas. Review feasibility, enrollment projections, timelines, budgets, resources, risks, and execution assumptions. Partner with Business Development, Clinical Operations, Finance, Medical, and regional teams to create customer-focused proposals, support sponsor meetings and bid defenses, and transition awarded studies into execution. Improve operational strategy methodologies, document decisions, and translate complex data into strategic recommendations.

Leads clinical development project delivery for the CNS/Neuroscience therapeutic area, overseeing portfolios, client relationships, business growth, financial performance, risk management, regulatory compliance, and resource allocation. Manages and develops senior project management leaders, drives strategic planning and operational excellence, and serves as executive sponsor for major accounts. Ensures projects meet timeline, budget, quality, ICH-GCP, and client satisfaction objectives.

Leads the Operational Strategy function for global clinical trial proposals across non-oncology therapeutic areas. Oversees team development, opportunity prioritization, operational strategy, feasibility, budgets, risk mitigation, proposal quality, bid defense, process governance, and strategic tool adoption. Partners with executive and cross-functional leaders to align study execution plans, sponsor requirements, organizational capabilities, and business objectives. Guides complex, high-value opportunities and drives consistent operational excellence across a geographically distributed portfolio.

Manages Clinical Leads and administrative staff overseeing clinical trial operations, compliance with GCP and regulatory requirements, staffing, performance, training, and operational processes. Conducts monitoring assessments, supports feasibility and business development activities, maintains relationships with clinical sites and vendors, contributes to SOP development, and resolves operational issues across clinical research projects.

Leads multi-country clinical trial teams, coordinating site management, monitoring, recruitment, training, data quality, safety reporting, and risk management. Develops clinical plans, reviews monitoring reports and data trends, oversees supplies and regulatory compliance, and ensures timely delivery of study milestones. Requires strong clinical research leadership, mentoring, communication, analytical, and problem-solving skills, with extensive CRA experience and knowledge of GCP and multi-country regulations. Senior leads additionally manage complex global trials, project financials, bid defenses, and process improvements.

Lead portfolio growth and oversee multiple global clinical development projects, ensuring regulatory compliance, client satisfaction, risk mitigation, financial performance, and delivery success. Manage and coach Project Directors and Project Managers, allocate resources, support business development, develop strategic offerings, and contribute to therapeutic-area planning. Serve as a senior client contact while monitoring project KPIs, budgets, timelines, profitability, and operational performance.

Lead planning and execution of clinical trials from site selection through closeout, ensuring compliance with ICH GCP, local regulations and SOPs. Manage budgets, vendors, CTMS/eTMF/IRT systems, recruitment, safety coordination, risk mitigation, change orders, and client communications to deliver projects on time and to budget.

Manage clinical trial projects end-to-end as primary Novotech client contact. Oversee timelines, budgets, vendors, site selection, recruitment, eTMF/CTMS maintenance, risk management, regulatory/GCP compliance, and team deliverables to ensure on-time, on-budget study delivery.

Lead and manage oncology clinical trial projects from site selection through closeout. Oversee timelines, budgets, vendors, regulatory/ethics submissions, patient recruitment, safety coordination, eTMF/CTMS maintenance, and ensure compliance with ICH‑GCP, SOPs and Project Agreements.

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.

Leads and manages Clinical Support staff, including Inhouse CRAs, through mentoring, onboarding, performance reviews, resource planning, and training. Ensures clinical trials follow ICH GCP, regulatory requirements, company SOPs, and project agreements. Supports project delivery, staff utilization, timesheet and expense approvals, recruitment, process improvement, and clinical operations activities. The Associate Manager may also perform billable Inhouse CRA responsibilities on assigned projects.

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.

Provide commercial, corporate, employment, privacy and compliance legal support for US operations of a global CRO. Lead drafting, review and negotiation of commercial agreements; manage disputes, investigations and external counsel; support acquisitions, due diligence, post‑acquisition integration, and legal/risk frameworks; advise stakeholders across functions and collaborate with global legal team to deliver pragmatic, commercially focused solutions.

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

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

Lead and continuously improve the global IT Compliance function for a CRO, ensuring IT governance, ISMS and ISO 27001 certification support, GxP computerised system compliance, audit readiness and vendor/third-party compliance oversight. Provide regulatory guidance, manage audit responses, run risk assessments, maintain compliance documentation, and drive remediation and continual improvement across IT and business stakeholders.