Clinical Trial Specialist - New Brunswick

We are seeking a dedicated Clinical Trial Specialist to join our team, focusing on protocol activation and study accrual. · This role involves collaborating with various departments to initiate and activate new clinical trial protocols, ensuring compliance with regulatory require ...

We are seeking a dedicated Clinical Trial Specialist to join our team, · focusing on protocol activation and study accrual.This role involves collaborating with various departments to initiate · and activate new clinical trial protocols, · ensuring compliance with regulatory requ ...

We are seeking a dedicated Clinical Trial Specialist to join our team, focusing on protocol activation and study accrual.This role involves collaborating with various departments to initiate and activate new clinical trial protocols, ensuring compliance with regulatory requiremen ...

We are seeking a dedicated Clinical Trial Specialist to join our team. · Collaborate with the Protocol Activation office to initiate and activate new clinical trial protocols. · Prepare and review study tools. · ...

We are seeking a dedicated Clinical Trial Specialist to join our team, focusing on protocol activation and study accrual.The successful candidate will facilitate communication between patients and research teams, manage protocol-specific orders, and ensure adherence to study guid ...

This role will support the Trialing Manager in executing research level yield trials on time, · with high precision and accuracy in a safe, compliant manner to generate the highest quality data. · A culture that celebrates diversity & inclusion, · Paid Vacation, · ,Paid Holidays ...

We are seeking a dedicated Clinical Trial Specialist to join our team. This role involves collaborating with various departments to initiate and activate new clinical trial protocols, · Collaborate with the Protocol Activation office to initiate and activate new clinical trial pr ...

This is a Contract to Hire position based out of Newark, NJ. · As Clinical Trial Specialist you will coordinate the initiation and activation of new clinical trial protocols. · ...

We are seeking a Clinical Trial Specialist to coordinate the initiation and activation of new clinical trial protocols. · Coordinate clinical trial protocols verification approvals · Prepare study tools such as binders diaries eligibility checklists flow sheets · ...

We are seeking a dedicated Clinical Trial Specialist to join our team, focusing on protocol activation and study accrual. This role involves collaborating with various departments to initiate and activate new clinical trial protocols, ensuring compliance with regulatory requireme ...

The Clinical Trial Specialist will support the planning and execution of clinical studies for AI-enabled disease detection. This role bridges clinical trial administration and site-facing activities, providing critical support in study execution, · data quality, and regulatory co ...

The Clinical Trial Results Reporting Specialist is responsible for creation of the clinical trial summary results report form for and EudraCT, the management of the review and approval process for these forms, and timely upload into the databases. · Identifies result summary data ...

The Clinic Trials Support Specialist responsible for coordinating and supporting the conduct of clinical research protocols and projects. · Prepare, submit, and maintain IRB and regulatory documentation. · Screen, enroll, and consent participants in collaboration with the Princip ...

The Clinic Trials Support Specialist responsible for coordinating and supporting the conduct of clinical research protocols and projects, with a primary focus on screening, enrolling, and monitoring patient participants. · ...

The Clinical Trial Disclosure Senior Specialist will provide operational support of redaction of clinical trial documents in accordance with evolving global regulations.CW can work from Summit West NJ or Lawrenceville NJ. · ...

The Clinical Trial Registration Specialist will report to the Clinical Trial Registration Lead and prepare and provide operational support for the registration of clinical trials into public registries in US and EU. · Drives the processes for assigned protocol registration activi ...

The Clinical Trial Disclosure Senior Specialist will provide operational support in redacting clinical trial documents according to evolving global regulations. · Manage and Coordinate redaction of clinical documents in accordance with EMA Policy 0070, Health Canada Public Releas ...

The Clinical Trial Registration Specialist will report to the Clinical Trial Registration Lead and prepare operational support for the registration of clinical trials into public registries in US and EU. · ...

The Clinical Trial Disclosure Senior Specialist will provide operational support of clinical trial document redaction according to evolving global regulations. · ...

+The Office of the Special Narcotics Prosecutor seeks a junior Trial Presentation and Evidence Support Specialist. · +Edit, enhance, prepare, and format audio and video evidence for use in hearings trials attorney review. · Collect digital surveillance footage from various system ...