Duties a CRC is required to perform include the following core functions, but are not all inclusive of:

· Direct interaction with and caring for human research participants

· Evaluate patients for inclusion and exclusions criteria on multiple protocols

· Schedule and coordinate all subject visits from screening to final follow up

· Perform chart review to evaluate for inclusion/exclusion criteria

· Perform venipuncture using universal precautions

· Perform EKG, vitals and any required trial specific procedures

· Ensure accuracy of data at each visit

· Adhere to GCP, ICH, HIPAA, NIH, FDA Regulations and SOPs guidelines

· Understand and working knowledge of being “Audit Ready at all times”

· Maintain regulatory documents to ensure most current documents are being utilized

· Support team members and cross-train to maintain knowledge of all delegated trials

· Create and maintain project timelines

· Maintain good relationships with Principal Investigator, site staff, patients and Sponsor/CRO

· Coordinate, record and manage subject data by maintaining accurate and complete source

· Complete case report forms and queries in a timely manner, per SOP guidelines

· Maintain records of receipt, storage and distribution of investigational product

· Attend and facilitate sponsor visits and audits

· Maintain accurate records of subject visits, to complete monthly study invoicing, per CTA

· Complete budget and CTA initial negotiation and amendments as necessary

Salary is based on experience.'

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Work Remotely

• No