Clinical Research Associate (CRA) - Part-time

sition of Clinical Research Coordinator. The ideal candidate will possess certification such as an MA, phlebotomy, or similar and have a strong desire to work directly with patients.lt;brgt;lt;brgt;lt;stronggt;Who We Arelt;brgt;lt;/stronggt;lt;brgt;
lt;/divgt;lt;divgt;Healing Kidneys Clinical Research is a Nephrology clinical trials focused company in Rare disease space that uses proprietary technology to:lt;brgt;Increase patient access to research trials within our communities,lt;/divgt;lt;divgt;Deliver superior clinical research enrollment metrics to Pharma sponsorslt;/divgt;lt;divgt;All with the goal of lt;emgt;Improving Patient Outcomes at the Point of Carelt;/emgt;. We want you to join us in doing just that.lt;brgt;lt;brgt;
lt;/divgt;lt;divgt;
lt;stronggt;Desirable Candidate:lt;brgt;lt;/stronggt;lt;brgt;
lt;/divgt;lt;ulgt;
lt;ligt;A lover of patient interaction and skilled at providing patient carelt;/ligt;
lt;ligt;A team player with a bias for action and an attitude that takes personal responsibilitylt;/ligt;
lt;ligt;Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.lt;/ligt;
lt;ligt;Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.lt;/ligt;
lt;ligt;Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherencelt;/ligt;
lt;ligt;An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and otherslt;/ligt;
lt;/ulgt;lt;divgt;Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studieslt;/divgt;lt;ulgt;lt;ligt;Energized by the idea of playing a role in the future of new therapy development in Nephrology amp; Rare diseaseslt;/ligt;lt;/ulgt;
lt;/divgt;
lt;div class=quot;benefitsquot;gt;
lt;divgt;lt;stronggt;Benefits:lt;/stronggt;lt;/divgt;
lt;ulgt;
lt;ligt;Bonus based on performancelt;/ligt;
lt;ligt;Company partieslt;/ligt;
lt;ligt;Flexible schedulelt;/ligt;
lt;ligt;Profit sharinglt;/ligt;
lt;/ulgt;
lt;/divgt;
lt;div class=quot;trix-contentquot;gt;
lt;divgt;Our clinical research group is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certification such as an MA, phlebotomy, or similar and have a strong desire to work directly with patients.lt;brgt;lt;brgt;lt;stronggt;Who We Arelt;brgt;lt;/stronggt;lt;brgt;
lt;/divgt;lt;divgt;Healing Kidneys Clinical Research is a Nephrology clinical trials focused company in Rare disease space that uses proprietary technology to:lt;brgt;Increase patient access to research trials within our communities,lt;/divgt;lt;divgt;Deliver superior clinical research enrollment metrics to Pharma sponsorslt;/divgt;lt;divgt;All with the goal of lt;emgt;Improving Patient Outcomes at the Point of Carelt;/emgt;. We want you to join us in doing just that.lt;brgt;lt;brgt;
lt;/divgt;lt;divgt;
lt;stronggt;Desirable Candidate:lt;brgt;lt;/stronggt;lt;brgt;
lt;/divgt;lt;ulgt;
lt;ligt;A lover of patient interaction and skilled at providing patient carelt;/ligt;
lt;ligt;A team player with a bias for action and an attitude that takes personal responsibilitylt;/ligt;
lt;ligt;Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.lt;/ligt;
lt;ligt;Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.lt;/ligt;
lt;ligt;Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherencelt;/ligt;
lt;ligt;An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and otherslt;/ligt;
lt;/ulgt;lt;divgt;Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studieslt;/divgt;lt;ulgt;lt;ligt;Energized by the idea of playing a role in the future of new therapy development in Nephrology amp; Rare diseaseslt;/ligt;lt;/ulgt;
lt;/divgt;