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Job type: Contract

Discipline: Clinical Trial Assistant (CTA)

Location: United States

Clinical Study Associate - Contract - Remote, MA

Work from anywhere and shape powerful clinical study that drive results! Enjoy the freedom of remote work while making a global impact.

��Ƶ is seeking a Clinical Study Associate to support the execution of clinical trials.

Primary Responsibilities:

This role involves coordinating various aspects of trial operations, ensuring data quality, and maintaining compliance with regulatory standards. You will work closely with cross-functional teams, sites, and vendors to facilitate smooth trial progression.

Skills & Requirements:

Resourceful and adaptable in dynamic environments.
Highly organized with strong multitasking abilities.
Collaborative team player with excellent communication skills.
Self-starter who takes initiative and drives deliverables independently.
Familiarity with GCP guidelines, SOPs, and clinical study phases.
Proficiency in Microsoft Word, Excel, PowerPoint, and basic database management.
Experience in a pharmaceutical, CRO, or clinical research setting.
Preferred: Medical-scientific experience in clinical research, and experience in monitoring, study coordination, or data handling.

The Clinical Study Associate's responsibilities will be:

Assist in trial execution, including site start-up, enrollment, monitoring, and data flow management.
Prepare essential study documents such as consent forms, site instructions, manuals, and pharmacy binders.
Track and review essential documents in the Trial Master File (TMF) for accuracy.
Monitor patient status, sample collection, and manage lab schedules and vendor coordination.
Collaborate with CROs and sites on sample handling and reporting.
Review monitoring reports, data queries, and site performance metrics.
Attend site visits and co-monitor with CROs.
Ensure data quality and address eligibility or protocol deviation issues.
Support investigator and vendor meetings, as well as feasibility assessments.
Review site contracts and budgets, and coordinate third-party vendor activities.

Compensation:

$56 to $63 per hour.

If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at j.cerchio@proclinical.com

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

��Ƶ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ��Ƶ is acting as an Employment Agency in relation to this vacancy.

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