Jobs at Novotech

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 role involves conducting lab analyses, managing lab logistics, drafting documents, ensuring compliance with regulations, and participating in training. Responsibilities also include maintenance and project management in a GLP environment.

Manage lab operations, conduct analyses, draft and review documents, oversee logistics, and ensure compliance with regulations. Support system validation and participate in training courses.

The Clinical Research Associate is responsible for managing site relationships, ensuring compliance with regulations, and monitoring clinical trials progress.

Conduct lab analysis, draft and review documents, manage lab logistics and inventory, and support analytical study project management. Ensure compliance with regulatory guidelines and maintain laboratory systems.

Conduct analyses according to SOPs, manage lab logistics, review documentation, and support GLP projects. Requires strong lab knowledge and communication skills.

The role involves conducting laboratory analyses, drafting and reviewing documents, managing lab logistics and compliance with regulatory standards, and participating in project management.

The Inhouse Clinical Research Associate supports the clinical team by managing study documentation, coordinating trials, and ensuring compliance with regulatory standards.

The Project Specialist assists the Project Manager in managing project deliverables, timelines, finance, and compliance in clinical research projects.

The Senior Business Development Director leads business growth through strategic planning, team development, resource management, and execution of clinical trial projects while fostering a positive team culture.

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 Business Development Director leads department operations, manages hiring, develops business processes, and maintains client relationships to achieve organizational goals in a CRO or biotech setting.

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

The Quality Assurance Manager oversees QA functions in bioanalytical and central laboratories, ensuring compliance with regulations, leading inspections, and driving continuous quality improvement.

The Clinical Document Specialist manages Trial Master File activities, ensuring adherence to SOPs, regulatory guidelines, and driving process improvements, while mentoring new team members.

Manage accounts receivable processes: prepare and post invoices, record customer payments (cash, check, wire), follow up on collections, resolve discrepancies, produce AR reports, review credit memos, and support process improvements to ensure timely, accurate payment recording and collections.

The Regulatory Start-Up Associate manages submissions for clinical trials, ensuring compliance with regulations and timelines while coordinating cross-functional efforts and stakeholder communication.

The Senior Document Management Associate manages Trial Master Files, ensures document quality, oversees uploads, trains team members, and supports audits.

The Inhouse Clinical Research Associate supports the clinical team's activities, manages documentation, ensures compliance, and assists with monitoring visits, specifically for clinical trials.