▪ Full scope of Clinical Research Associate I responsibilities▪ Train entry level Clinical Research Associates with In-Field Training Visits. ▪ Reconcile investigator site files to confirm that sites are audit ready at all times.▪ Review investigational product accountability logs to monitor the administration and storage of study drugs.

▪ Full scope of Clinical Research Associate I responsibilities.▪ Collaborate with Quality Assurance to investigate critical deviations and serious site non-compliance findings. ▪ Work in close collaboration with Clinical Leads to achieve study objectives. ▪ Utilize risk-based monitoring to resolve and mitigate site issues.

▪ Perform site selection, initiation, routine monitoring, pharmacy, and close-out visits per the monitoring visit plans.▪ Provide site support to meet recruitment goals.▪ Conducted source data review and verification to ensure that sites follow ALCOA principles.▪ Create site visit and contact reports to accurately records the conduct of clinical trials.

▪ Review research consents and protocols to ensure that research studies are compliant with federal regulations.▪ Coordinate the submission of regulatory documents required to open new research trials.▪ Track the expiration and renewal dates of regulatory approvals. ▪ Serve as a guide to physicians/researchers in the design of oncology treatment studies and pharmaceutical trials.

▪ Coordinated the collection, distribution, and storage of data obtained during clinical trials.▪ Was responsible for keeping clinical trials on track with clinical objectives.▪ Facilitated the research of oncology trials by collecting medication toxicities.▪ Ensured Serious Adverse Event (SAE) reporting was completed per protocol specifications.

▪ Provided technical support to new clinic providers and taught them how to utilize the EMR system.▪ Reviewed providers’ documentation to ensure proper visit charges and Dx codes were applied to patient visits.▪ Co-managed 5 ambulatory clinics in EMR conversion project.▪ Assisted providers and all hospital/clinical staff with any EMR questions and technical problems.

▪ Responsible for processing all pediatric referrals in the clinic.▪ Obtained insurance authorizations for every patient’s specialty visits.▪ Followed up with patients' specialty visits for consultation and progress notes.▪ Scanned medical documents into patients' electronic health records.

▪ Ensured availability of treatment information by filing and retrieving patient records▪ Registered new patients and updated existing demographics▪ Checked insurance eligibility according to office guidelines▪ Obtained referrals and pre-authorizations as required for providers.

▪ Supervised all CNAs on shift.▪ Managed medication administration for all residents/patients in the community.▪ Monitored terminally ill patients/residents and administered hospice medications as needed.▪ Responsible for drug inventory including narcotics.▪ Filed incident reports per state and federal guidelines.

▪ Triaged patients and took vital signs.▪ Administered medications including injections.▪ Practiced basic wound care and bandaging.▪ Assisted in all outpatient procedures.