An experienced and qualified Clinical Research Coordinator/study Nurse is essential to all successfully enrolled, protocol and ICHGCP compliant clinical trials. Not all settings have access to this resource in-house. An excellent solution with proven results is to engage a specialist study coordinator dedicated to your project on a contract basis.Dedicated Clinical Research Coordinators are not just dedicated in their attitude but also dedicated to your project, not stretched thin across several protocols. Dedicated CRC is on site when needed for patient visits and coordinating operational tasks remotely. No overheads.

Clinical Site Specialist. Hands on solutions to site challenges. Patient recruitment a specialty.Working independently to facilitate clinical trials in Australia and New Zealand by providing expertise to all members of clinical research teams in both private and public settings overcome obstacles in all areas from HREC approvals, ICHGCP compliance, clinical site set up and ongoing support, patient visits, data entry.

Alternate dispute resolution practitioner. Working respectfully and with compassion to help resolve issues that might be causing distress. Including conflict in the workplace, neighbourly disputes, elderly disputes . A passion for relationship problems such as adults and adolescent children communication break down. Confidential, affordable and very worthwhile.

Because your health is everything! Passionately working to build partnerships with leaders in clinical research in support of patient recruitment to clinical trials in Australia and New Zealand.

Coordination of all clinical trial activities from site selection to CTA negotiations, HREC submission, study visit conduct, safety reporting, study closeout and archiving.Phase II, III and IV in Type 1, Type 2 Diabetes and Obesity as well as associated complications such as cardiovascular disease, peripheral nephropathy, hyperlipidaemia.Experience with devices such as Insulin pumps and continuous Glucose monitoring.

Clinical Trial Coordination of investigator initiated as well as Pharmaceutical Company Sponsored Clinical Trials in Pain Medicine as well as other areas including vaccine and Device Trials. Experienced in Phase I to Phase IV Clinical Trials.Coordination of all activities from feasibility to CTA negotiations, Ethics Submission, participant recruitment and conduct of study visits. Adverse Event and Serious Adverse Event Reporting.CRF Entry, Drug accountability, Closeout and Archiving

Collection and processing of Pathology samples including Urine Drug Screen, Routine Biochem and Haematology, swabs, ECG, spirometry.

Disability/Mental Health Nursing in Hospital and Community settings.