**ALL CV´s MUST BE SUBMITTED IN ENGLISH IN ORDER TO BE REVIEWED!** Independently manage essential regulatory documentation (as applicable) for submission to country/regional/site Institutional Review Boards (IRB),…
The Study Activation Manager leads global study start-up and site activation strategy and realization for assigned Phase I–IV clinical trials. This role is accountable for driving the activation path from award through…
The Clinical Project Manager III (CPM III) is responsible for execution and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, cost, and quality performance are met. The…
This position is responsible for selling CTI clinical trial and regulatory and scientific affairs consulting services, including Phase I-III clinical trials and regulatory consulting services spanning pre-IND to NDA…
**ALL CV´s MUST BE SUBMITTED IN ENGLISH IN ORDER TO BE REVIEWED!** Provide administrative and regulatory assistance to the Regulatory Affairs Study Start-up (RASSU) Department.
The Clinical Project Manager II (CPM II) is responsible for management and oversight of assigned clinical research trials (Phase I through Phase IV) to ensure client’s goals of time, cost, and quality performance are…
The Clinical Project Coordinator position is responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, budgets and quality standards are being achieved. **Please note…
Responsible for management and oversight of assigned clinical research trials (Phase I through Phase IV) to ensure client’s goals of time, cost, and quality performance are met. The CPM II is expected to perform most…
Responsible for project activities associated with monitoring functions of Phase I through Phase IV clinical research studies and Real World Evidence (RWE) studies, as an expert in the drug development process,…
Independently manage essential regulatory documentation (as applicable) for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other…
Manage essential Regulatory documentation (as applicable) for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for…
The Clinical Project Manager (CPM) is responsible for execution and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, cost, and quality performance are met. The CPM is…
** Please do not apply if you are not fully eligible to work in Australia. CTI doesn't offer Sponsorship ** Responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring…
The Financial Systems Analyst is responsible for the administration, optimization, and support of global financial systems. This role supports Finance, IT, and business stakeholders to ensure systems are effectively…
Responsible for management and oversight of assigned laboratory clinical trials/projects to ensure client’s goals of time, cost, and quality performance are met. The LPM is expected to perform most tasks independently,…
The Information Technology (IT) Support Specialist I provides first level use support to CTI Employees and sets up and maintains all phone and computer equipment.
Manage essential regulatory documentation (as applicable) for submission to country/regional/site Institutional Review Boards (IRB)Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for…
The Senior Clinical Project Manager is responsible for execution and oversight of assigned clinical trials (Phase I through Phase IV) to ensure client’s goals of time, cost, and quality performance are met. The Senior…
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