Job Information
Robert Half Project Coordinator - Paralegal in Danvers, Massachusetts
Description
Job Title: Clinical Research Coordinator - Paralegal Cordinator
Location: Robert Half Legal
Job Overview:
The Clinical Research Coordinator (CRC) at Robert Half Legal will be primarily responsible for coordinating and overseeing the collection and management of patient clinical data for participation in clinical studies. This includes ensuring timely collection and management of protocol-related samples, maintaining regulatory adherence to state, federal and IRB requirements, screening patients for protocol eligibility, obtaining informed consent, and participant registration.
Key Duties and Responsibilities:
Manage the entire research study start-up process from receiving protocols to the Scientific Review Committee and IRB submissions.
Carry out data reporting and management, including gathering of source documents, development of case report forms, adverse reactions reporting, filing, and archiving of study records, and resolution of data queries.
Prepare and complete regulatory related reports and IRB submissions, maintain and organize study regulatory binders, and enter required study data on a continual basis.
Ensure all study-related samples are collected, prepared, and dispatched according to the protocol requirements and IATA/DOT regulations.
Organize and prepare for both internal and external auditing and study monitoring visits.
Handle coordination and management of clinical studies, including frequent communication with sponsors and regulatory authorities.
Oversee close-out of studies, including contributing to research articles, audit preparation, and communication with regulatory agencies and other involved disciplines.
Screen and select participants for protocol eligibility, obtain informed consent, recruit and register study participants, manage data collection, and report adverse events.
Interact with study participants as per the protocol and/or study team directives.
About Robert Half Legal:
Robert Half Legal is a premier legal employment agency providing a wide range of legal professionals, on a temporary, project, and full-time basis. We specialize in the placement of attorneys, paralegals, legal administrators, and other legal professionals. With a strong commitment to ethics, expertise, and innovation in the legal field, as a Clinical Research Coordinator, you will be part of the team that contributes to the advancement of healthcare.
Requirements Clinical Trial Agreement, Contract Administration
Robert Half is the world’s first and largest specialized talent solutions firm that connects highly qualified job seekers to opportunities at great companies. We offer contract, temporary and permanent placement solutions for finance and accounting, technology, marketing and creative, legal, and administrative and customer support roles.
Robert Half works to put you in the best position to succeed. We provide access to top jobs, competitive compensation and benefits, and free online training. Stay on top of every opportunity - whenever you choose - even on the go. Download the Robert Half app (https://www.roberthalf.com/us/en/mobile-app) and get 1-tap apply, notifications of AI-matched jobs, and much more.
All applicants applying for U.S. job openings must be legally authorized to work in the United States. Benefits are available to contract/temporary professionals, including medical, vision, dental, and life and disability insurance. Hired contract/temporary professionals are also eligible to enroll in our company 401(k) plan. Visit roberthalf.gobenefits.net for more information.
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