is seeking to hire a Clinical Research Coordinator for our client in Brandon, FL!

Benefits Available!
Weekly Pay!
6 Month Contract

Pay Rate - $35.86/hr
1st Shift: Monday-Friday, 7am-4pm

Job Description
The Research Coordinator position is responsible for Coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a fundamental understanding of human subject research.

Major Responsibilities
· During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.
· Performs routine operational activities for multiple research protocols
· Liaise between site research personnel, industry sponsors, and Supervisor
· Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
· Coordinates schedule of assessments from initial submission of feasibility until study closeout
· Reviews the study design and inclusion/exclusion criteria with physician and patient
· Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
· Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data
· Creates study specific tools for source documentation when not provided by sponsor
· Collects, completes, and enters data into study specific case report forms or electronic data capture systems
· Generates and tracks drug shipments, device shipments, and supplies as needed
· Ensures timely and accurate data completion
· Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations
· Communicates all protocol-related issues to appropriate study personnel or manager
· Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required
· Reviews and responds to any monitoring and auditing findings

Required Education and Experience
Bachelors degree in a related field
1+ years of relevant experience

Clinical Research Coordinator certification preferred.

Knowledge, Skills, and Abilities

Knowledge
· Knowledge of organizational policies, standard operating procedures, and systems
· Emerging understanding and application of ICH guidelines and the Code of Federal Regulations within the clinical research environment.
· Basic understanding of medical terminology

Skills
· Effective communication skills
· Strong organizational skills and time management
· Basic clinical trial procedures, including ECG acquisition, phlebotomy, and specimen processing, handling, storing, and shipping

Abilities
· Interpersonal skills
· Self-motivated
· Meticulous eye for detail