Novotech

The Senior Investigator Grant Specialist is responsible for the development, negotiation, and management of investigator grants and site payments for global clinical trials. This role serves as a subj

The Statistical Programmer II is primarily responsible for undertaking all statistical programming tasks on one or more clinical studies under the supervision of more senior Statistical Programmers an

The core responsibility for this position is as a member of Novotech's Data Management group. The Clinical Data Manager's (CDM's) role is to control all aspects of data management and to ensure compli

The core responsibility for this position is as a member of Novotech' s Data Management group. The Senior Clinical Data Manager's (SCDM's) role is to control all aspects of data management and to ensu

Responsible for day-to-day data processing operations for data management projects, including CRF (or other study data document) tracking, entry, and filing. Provides administrative and project manage

The core responsibility for this position is as a member of the Data Management department at Novotech. The Clinical Data Programmer-II (CDP-II) will be responsible for programming activities on clini

The Senior Clinical Data Programmer Analyst (SCDPA) is responsible for data analysis and business intelligence activities related to study related clinical and operational data for the purpose of faci

The Clinical Document Specialist (CDS) will provide support for Trial Master File (TMF) activities to the clinical teams for assigned projects. This role will be responsible for the overall management

The Investigator Grants Specialist will provide support to project team in managing the payment for investigators and developing the Investigator grant using the standard system such as Grant Plan. Th