Clinical Research Coordinator

Valkyrie Clinical Trials (VCT), a Flourish Research Company, is a leading Oncology multi-site clinical research network with expertise in Oncology research. VCT approaches clinical research with a deep sense of humanity, compassion, and sincere kindness. VCT was founded by leading Clinical Oncologist, Dr. David Berz, and has multiple sites spanning California in Century City, Panaroma City, and Murrieta, and has recently expanded to Denver, Colorado.

Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status.

We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities.

WESEEYOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

We are actively hiring a Clinical Research Coordinator to support our Valkyrie Clinical Trials Denver, Colorado site.

LOCATION
:
Onsite
FLSA
:
Non-Exempt
HOURS
:
Monday to Friday, Day Shift, 40 hours per week
COMPENSATION
: $27-44 per hour (depending on experience)

• Read,understand,andensurethecompletion ofallprotocolrequiredpatientvisitsandprocedures
• Clearly and concisely document patient assessments,treatments,observations, test results and other study related information per federal regulations, protocolrequirementsand GCPGuidelines.
• Obtainpatientinformedconsent, and reconsent as required,accordingtofederalregulations,GCPandIRBrequirementswhile educating patients on study requirements, timelines, and visit expectations.
• AsSenior CRC, lead and mentor otherresearchstaffand serve as an escalation point and SME.
• Isdiligentinenrolling qualifiedstudyparticipantsintoappropriateprotocolswithinthe sponsor’s timeline while following regulations and rules governing medical ethics, IRB, GCP and ICH guidelines.
• Completeallrequired traininginatimelymanner.
• Scheduleandconductpatientvisitsaccordingtoprotocol requirementsandtimelines.
• Maintainwrittensource documentation of patient visits and protocol relatedactivitiesper ALCOA guidelines
• Accurately complete case report forms (CRFs &/or eCRFs) and/or worksheetsandrespond toqueriesgenerated by thesponsorina timely manner
• Maintain confidentialityofallpatient and protocol activities and informationasappropriateand as boundby
  
  Confidentiality Agreements with Valkyrie/Flourish Research,between
  
  Valkyrie/Flourish and sponsors, and between
  
  Valkyrie/Flourish and other entities, as well as HIPAA regulations.
• Promptly document andreportadverseeventstosupervisorand/or Principal
  
  Investigator/Sub-Investigatorasdeemednecessary.
• Report Serious Adverse Events (SAEs) to sponsor within 24 hours of becoming aware of the SAE. Also report the SAE to the supervisor, Principal Investigator and/or Sub-Investigator immediately.
• Account for clinical trial materials (i.e., CRFs,studydrug, lab supplies, and/or other required items) and ensure availability of appropriate amounts for the conduct of the study.
• Maintain ongoing communication with
  
  Team Lead I;
  Team Manager/Research Manager;
  
  Principal Investigator;
  Sub-Investigators and other peopleassistingwiththetrial anddocumentingthese communications…