Join The CTI Team Jobs in United States

Independently manage essential regulatory documentation for submission to country/regional/site Institutional Review Boards (IRB), Ethics Committees (EC), Competent Authorities (CA) and/or other Regulatory Bodies for all clinical studies performed globally. · ...

We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department. · Advance Your Career – We support ...

This person will serve as the primary CTI Clinical Data Management (CDM) contact with sponsors and represent the DM group on CTI project teams. · Perform and/or direct activity of CDM team members to complete project deliverables on schedule according to quality standards, requir ...

The Governance Coordinator is responsible for providing organizational and administrative support to CTI's governance structure and associated procedures. The role involves managing client governance frameworks, preparing governance materials, supporting new client onboarding and ...

Assist in the daily functions and operations of the Accounting Department within the assigned specialty area. · ...

The Director, Study Start-Up & Process Improvement is responsible for leading and optimizing cross-functional processes that support site activation activities. · This role serves as the central point of responsibility in driving clinical trial site activation cycle time, · colla ...

Build and execute multi-year global category strategies for that align with CTI's growth, risk posture, and budget targets Conduct market intelligence benchmarking and should-cost analysis to inform sourcing decisions Define category KPIs savings targets and value levers cost qua ...

The Project Manager Laboratory Services will be responsible for planning and implementing assigned laboratory clinical trials/projects; may function as a global lead, where applicable. · ...

The Clinical Project Manager III (CPM III) is responsible for execution and oversight of assigned clinical trials to ensure client's goals of time, cost, and quality performance are met. · ...

This position is responsible for selling the full range of Real-World Evidence (RWE) services at CTI and will lead the identification and development of new opportunities for the RWE Organization. · Secure and maintain relationships with qualified targets and decision makers with ...

This Regional Clinical Monitoring Executive Director will lead regional CM staff for high-quality site management and monitoring of clinical trials. They will serve as senior internal CM contact for engagement with other company leaders and client representatives. ...

A Clinical Programmer will support the design development and validation of clinical trial databases. · Act as a primary database architect for client clinical databases using Medidata Rave OmniComm TrialMaster or other database applications as needed for Clinical TrialsCreate da ...

The Executive Medical Director will lead a therapeutic portfolio through medical development expertise. · Drive growth of a therapeutic area portfolio through medical development expertise. · Participate in clinical trials. · ...

As Global Vice President, Commercial Sales, you will report to the CCO and be responsible for developing commercial and business development strategies that are optimized for both short-term results and long-term strategy. · ...

Perform moderate and high complexity testing, as defined by CLIA, while following the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of test results. · ...

+Job summary · Oversees the department and manages all regulatory aspects of clinical trials conducted at the Clinical Research Center (CRC). Ensures regulatory compliance with FDA, ICH-GCP, and IRB regulations. · ...