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Recently posted jobs
Biotech
The Application Specialist CSV/SLDC leads GxP validation and software testing strategies, ensuring compliance in regulated industries through documentation, testing, and audits.
Biotech
The Accounts Payable Associate processes vendor invoices using Concur, ensuring accuracy and timely payments while maintaining relationships with suppliers and stakeholders.
Biotech
The Investigator Grants Specialist supports project teams in managing investigator payments, processing site budgets, and ensuring timely payments using industry-standard systems. Responsibilities include tracking payments, developing investigator grants, communication with stakeholders, and adherence to Novotech's guidelines.
Biotech
The Document Management Associate supports clinical teams by managing Trial Master Files (TMF) through tracking, reviewing, and maintaining electronic and paper documentation according to guidelines, ensuring quality and compliance during clinical study processes.
Biotech
The Senior Document Management Associate manages TMF activities for clinical teams, ensuring document quality, compliance with regulations, and mentoring team members.
Biotech
The Clinical Data Manager plans, conducts, and manages data for clinical trials, ensuring compliance with guidelines and overseeing all data management aspects.
Biotech
The Senior Clinical Lead Analyst supports project delivery by monitoring clinical performance, ensuring compliance with regulations, and managing project data effectively. They collaborate with the Clinical Lead to evaluate and report on KPIs, oversee site-level performances, and ensure quality in clinical protocols.
Biotech
The role requires managing social media presence, including organic and paid efforts, optimizing performance, and collaborating across teams to drive brand awareness and engagement.
Biotech
The Clinical Document Specialist manages Trial Master File activities, ensuring adherence to SOPs, regulatory guidelines, and driving process improvements, while mentoring new team members.
Biotech
The Senior Document Management Associate manages Trial Master Files, ensures document quality, oversees uploads, trains team members, and supports audits.
