Apply on Employer Site

American Vision Partners · 21 hours ago

Jr. Clinical Research Coordinator

US-AZ-Mesa

Full-time

Onsite

New Grad, Entry Level

American Vision Partners (AVP) is focused on building the nation’s largest and most comprehensive eye care practices. As a Junior Clinical Research Coordinator, you will assist with the management and coordination of all aspects of conducting clinical trials, ensuring protocol compliance and patient safety.

Health CareMedical

Responsibilities

Acts as a representative of clinical research and as liaison between investigators, other study staff, primary care providers, IRB and sponsor

Screens, consents, enrolls and follows study subjects ensuring protocol compliance and close monitoring while subjects are on study utilizing Research Nurses’ oversight for help with clinical decision making

Responsible for all data and source documentation, and adverse experience reporting

Responsible for following departmental policies

Responsible and for assuring proper billing for research subjects. Assures that charges for tests and treatments are appropriately communicated and processed

Assists as needed in preparing study for submission to IRB and ensures all regulatory documents are completed

Attends study-related meetings as appropriate

Travels between RCA research offices as needed for patient and business needs

Develops screening/enrollment/follow up mechanisms

Ensure adherence to protocol requirements

Schedules and performs patient procedures, assessments, evaluations and testing as required by the protocol, including but not limited to blood sample collection, processing and shipping, ECG, vital signs, etc., as applicable

Organizational maintenance of all aspects of the trial, including but not limited to timeliness in completing CRFs, reporting adverse events, managing caseload and study files

Responsible for quality data entry into sponsor’s database (electronic data capture systems or paper CRFs) and query resolution

Ensures proper study drug administration, compliance and accountability, including receipt and , storage and dispensing

Ensures patient safety and ensures coordination of patient care as needed

Assists with maintenance of regulatory documents, IRB reporting and submissions of amendments, renewals, etc

Assists with study initiation visits, monitoring visits, closeout visits and audit visit, ensuring all study documentation and study issues are addressed

Communicates regularly with the Manager of Clinical Research at RII and Principal Investigators about study related issues

Ensures compliance with department standards and all federal regulations and international guidelines of good clinical practice

Maintain job related certifications (IATA, Human subjects, subjects’ protection training, GCP, and protocol specific required training)

Active in acquiring professional growth by obtaining CRC certification when eligible and joining a professional association such as SOCRA or ACRP

Performs other duties and responsibilities as required

Promotes a positive work environment and works to be an integral member of the team

Encourage a team-oriented environment supporting the AVP Mission, Vision and Core Values

Participate in on-going training and continuing education

Show respect and deal appropriately with co-workers, patients, and visitors

Perform any and all duties assigned

Qualification

Clinical research coordinationRegulatory complianceData managementClinical experienceIATA certificationGCP trainingTeamworkCommunication skillsOrganizational skillsProblem-solving