CTI Clinical Trial and Consulting Services

The Patient Recruiter is responsible for telephone interviewing, pre-screening, qualifying and setting appointments for patient's clinical study participation. This position is office based at our headquarters…

HybridNorth AmericaFull-time

2 weeks ago

Study Activation Manager

data-quality gcp process-improvement

What you'll do: Develop and lead the global study start-up and site activation strategy for assigned trials, including activation assumptions, country and site sequencing, critical path dependencies, milestone…

2 weeks ago

Clinical Project Manager III/ Senior CPM (level dependent on experience)

UKSenior

United Kingdom

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…

3 weeks ago

Director, Business Development & Client Management - Level Dependent On Experience

LATAM, North America

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…

3 weeks ago

Clinical Project Manager II

MENA

Egypt

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…

4 weeks ago

Clinical Project Coordinator

North America

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…

4 weeks ago

Clinical Project Manager II

MENA

Egypt

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…

Senior Regulatory Affairs Study Start Up Specialist

North AmericaSenior

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…

Regulatory Affairs Study Start Up Specialist II

APAC

Australia

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…

Clinical Project Manager

APAC

Australia

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…

Clinical Project Coordinator/Clinical Trial Assistant

APAC

Australia

** 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…

Financial Systems Analyst

Europe

Portugal

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…

Project Manager, Laboratory Services

Europe

Spain

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,…

2 months ago

IT Support Specialist

HybridEuropeFull-time

Portugal

What You'll Do: Provide first-level support to all CTI employees for computer system hardware, software, and telecommunications Procure and install all new electronic devices such as PCs; set up as required Meet…

2 months ago

Regulatory Affairs Study Start Up Specialist II

HybridAPACFull-time

South Korea

What You'll Do Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements and document any activity discovered; notify Project…

gcp xml

HybridNorth AmericaFull-timeSenior

9 months ago

Senior Clinical Project Manager - up to $15K sign-on bonus!