Jr. Clinical Research Coord

• 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 sponsors 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.

• Associate or Bachelors Degree or working toward one


• Clinical experience in Retina or other optical care


• Prior research experience


• Current IATA Human Subjects protection training or GCP training highly desirable
  
  
  
  • Certificates Licenses Registrations:
  
  
  
  


• Specialty certification such as CCRC preferred

Your health happiness and your future matters! At AVP we offer everything from medical and dental insurance significant eye care discounts child care assistance pet insurance continuing education funds 401(k) paid holidays PTO Sick Time opportunity for growth and much more!