Clinical Research Coordinator

Position: Clinical Research Coordinator 1
* Performs various aspects of clinical research, such as collecting and processing specimens, interviewing subjects, taking vital signs, and contributing to the case report.
* Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
* Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
* Responsible for all aspects of research projects involving patients on IRBs.
* Organizes recruiting, consenting and scheduling research subjects.
* Oversees development and amendments of study protocols.
* Directs collection and analysis of bio specimens collected for clinical trial.
* Works collaboratively with the team and collaborators.
* Develops data collection tools.
* Maintains and builds databases; maintains bio specimen storage.
* Provides general administrative supports including maintenance of documentation.
* Writes and updates all protocols for specimen collection and processing. Ensures compliance with institutional, state, and federal regulatory policies, procedures, directives, and mandates.
* Processing and banking of bio specimens (serum, plasma, ascites, tumor, benign tissues) and extraction of DNA.
* Accountable for all tasks in basic clinical studies.
* Assists with various professional, organizational, and operational tasks under direct supervision.
* Supports quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
* Uses knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples.
* Performs other related work as needed.
* Experience and knowledge in relevant scientific field strongly preferred.
* Experience and knowledge of research techniques or methods strongly preferred.
* Experience contributing to research publications strongly preferred.
* Demonstrates working knowledge of research regulatory policies, procedures, and compliance requirements, including human subjects protections.
* Applies analytical thinking to review study materials, identify inconsistencies, and support accurate data collection and documentation.
* Uses sound judgment and basic problem solving skills to address routine study related issues and escalate concerns appropriately.
* Maintains strong attention to detail to ensure accuracy in data entry, specimen handling, and regulatory documentation.
* Effectively organizes and prioritizes multiple tasks, maintaining orderly and audit ready files and tracking systems.
* Communicates clearly and professionally in both written and verbal interactions with research participants and team members.
* Works independently on assigned tasks while collaborating effectively within a multidisciplinary research team.
* Demonstrates proficiency in Microsoft Office applications to support data management, documentation, and reporting.
* Adapts to shifting study priorities, protocol updates, and evolving research needs with flexibility and professionalism.
* Applies basic medical and research terminology accurately in documentation and communication.
* Knowledge of Microsoft Office.
* Lab environment.
* Ability to stand for extended periods of time.
* Able to move greater than 15 LBS as needed on the job.

When applying, the document(s)
** MUST
* * be uploaded via the
** My Experience
** page, in the section titled
** Application Documents
** of the application.

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