Jobs at Novotech

Lead and manage clinical trials from site selection to closeout, ensuring compliance with ICH GCP and local regulations, meeting timelines and budgets, coordinating cross-functional teams, vendors, data and safety activities, and maintaining project documentation (CTMS/eTMF). Act as primary client contact and drive recruitment, risk mitigation, and audit readiness.

Lead global IT service delivery and Enterprise Service Management (ESM), manage regional service teams, own ServiceNow, enforce SLAs/KPIs, implement QA and compliance frameworks, oversee incident/problem/request/knowledge processes, drive continuous improvement and automation, manage budgets and stakeholder reporting, and ensure regulatory validated system adherence.

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.

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

Manage site relationships and ensure trials follow ICH GCP, local regulations, and SOPs. Perform site monitoring (selection, initiation, monitoring, close-out), support regulatory/ethics submissions, drive site recruitment, and collaborate with internal teams to ensure accurate, complete, verifiable trial data and participant safety.

Coordinate full recruitment lifecycle and HR administration: onboarding/offboarding, employee records, performance management support, reporting, payroll tracker updates, benefits/compensation support, policy counseling, and HR systems administration.

Manage all aspects of clinical trial data management, ensuring GCDMP and SOP compliance. Plan and execute database design, validation, data cleaning, develop data management documentation, liaise with clients and vendors, support protocol development, and supervise/train junior staff.

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.

Manage and monitor assigned clinical trial sites independently, ensure participant safety and data integrity, drive site performance and recruitment, build relationships with investigators and site staff, and partner with sponsors and internal teams to deliver Phase I-III studies.

Manage and support conduct of multi-country clinical studies, liaise between PM and local teams, ensure compliance with ICH GCP and local regulations, oversee vendor and site activities, support budgeting and reporting, and act as PM backup or lead for smaller studies.

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.