Healthcare Support
Senior clinical research coordinator
Healthcare Support, Chicago, Illinois, United States, 60290
Senior Clinical Research Coordinator – Oxnard, CA
HealthCare Support is actively seeking a
Senior Clinical Research Coordinator
to fill a job opening. This role’s location is
in Chicago, IL
(this role may periodically require travel to a secondary site to provide support or temporary coverage as needed).Daily Responsibilities for Senior Clinical Research Coordinator:
Manages and oversees the day-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants)Regularly interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocolCreates standard operating procedures (SOPs) that adhere to all Food and Drug Administration (FDA) and Office for Human Research Protections (OHRP) regulationsContributes to the training of clinical trial staff and accountable for compliance with the operational requirements of the clinical trialFunction as participants’ primary point of contact, keeping them informed on the study progress, and facilitate involvement of other study team members, as needed (e.g., notify Principal Investigator of safety events)Manage participant visit scheduling and technical troubleshooting, escalating issues to the appropriate individual(s)Solicit and record information regarding safety events and preparing safety event documentation for review by the Principal InvestigatorProvides accurate and timely data collection, documentation, entry, and reporting in both Sponsor and Walgreens databasesSupports the regulatory staff in the maintenance of regulatory documents in accordance with Walgreens SOPs and applicable regulationsCommunicates and collaborates specific study requirements to the research team, including internal and external parties, sponsor, monitors, PI, and study participantsMaintain regular contact with the Principal Investigator and team to review study details (e.g., progress, adverse events, enrollment)Maintain study supplies and issue appropriate participant stipendsEnsures appropriate credentialing and training of the study teamFacilitate meetings with the study monitors, auditors, and investigatorsEnsure timely response to queries and documentation of study-related issuesIf applicable, disburses investigational product, manages inventory of equipment and study supplies, and provides patient education regarding administration, as necessaryContribute to the development and implementation of tools, processes and training to enhance the administration and execution of clinical studies (e.g., GCP, ALCOA-C)Accountable for site compliance with subject safety reporting, escalate issuesDemonstrate professionalism and apply basic leadership practices in all aspects of the roleTrain and support study team members on a range of communication and teamwork best practicesPerforms other duties related to the clinical trials as delegated by the Principal InvestigatorThe shifts for the position will be Monday to Friday, 8am to 5pmThis is a one-year contract role, with a potential for perm placement afterwardsRequired Qualifications for Senior Clinical Research Coordinator:
High School Diploma/GED3+ years in clinical trial spaceWorking knowledge of ICH-GCP, US CFR, and HIPAA regulationsExperience working independently and making appropriate decisions to operationalize and move clinical trials forwardExperience overseeing multiple clinical trials concurrently, while maintaining attention to detailExperience prioritizing tasks and resources, meeting deadlines, and being adaptable to changing prioritiesProficient with phlebotomy (certification not mandatory). CRCs are expected to draw bloodBenefits for Senior Clinical Research Coordinator:
Immediate enrollment in Health InsuranceDental InsuranceLife InsuranceEmployee Assistance Program (EAP)Access to Investment AccountsCareer and educational tools within our Ingenovis ACT (Advocacy) ProgramPay: $48 to $55 an hour
Interested in being considered?
If you are interested in applying to this position, please click Apply Now for immediate consideration.For additional consideration, please email a copy of your resume to mitchell.reiter@healthcaresupport.com with your phone number, the job title and location, and our recruiters will reach out.Healthcare Support Staffing, LLC is an equal employment opportunity employer and will consider all qualified applicants without regard to race, color, religion, disability, sex, sexual orientation, gender identity, national origin, protected veteran status, or any other characteristic protected by applicable local, state, or federal law.
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HealthCare Support is actively seeking a
Senior Clinical Research Coordinator
to fill a job opening. This role’s location is
in Chicago, IL
(this role may periodically require travel to a secondary site to provide support or temporary coverage as needed).Daily Responsibilities for Senior Clinical Research Coordinator:
Manages and oversees the day-to-day operations in the administration of clinical trial activities at the site-level (i.e., direct interactions with study participants)Regularly interfaces with current and potential clinical trial participants to determine eligibility and consent of study participants in alignment with clinical trial protocolCreates standard operating procedures (SOPs) that adhere to all Food and Drug Administration (FDA) and Office for Human Research Protections (OHRP) regulationsContributes to the training of clinical trial staff and accountable for compliance with the operational requirements of the clinical trialFunction as participants’ primary point of contact, keeping them informed on the study progress, and facilitate involvement of other study team members, as needed (e.g., notify Principal Investigator of safety events)Manage participant visit scheduling and technical troubleshooting, escalating issues to the appropriate individual(s)Solicit and record information regarding safety events and preparing safety event documentation for review by the Principal InvestigatorProvides accurate and timely data collection, documentation, entry, and reporting in both Sponsor and Walgreens databasesSupports the regulatory staff in the maintenance of regulatory documents in accordance with Walgreens SOPs and applicable regulationsCommunicates and collaborates specific study requirements to the research team, including internal and external parties, sponsor, monitors, PI, and study participantsMaintain regular contact with the Principal Investigator and team to review study details (e.g., progress, adverse events, enrollment)Maintain study supplies and issue appropriate participant stipendsEnsures appropriate credentialing and training of the study teamFacilitate meetings with the study monitors, auditors, and investigatorsEnsure timely response to queries and documentation of study-related issuesIf applicable, disburses investigational product, manages inventory of equipment and study supplies, and provides patient education regarding administration, as necessaryContribute to the development and implementation of tools, processes and training to enhance the administration and execution of clinical studies (e.g., GCP, ALCOA-C)Accountable for site compliance with subject safety reporting, escalate issuesDemonstrate professionalism and apply basic leadership practices in all aspects of the roleTrain and support study team members on a range of communication and teamwork best practicesPerforms other duties related to the clinical trials as delegated by the Principal InvestigatorThe shifts for the position will be Monday to Friday, 8am to 5pmThis is a one-year contract role, with a potential for perm placement afterwardsRequired Qualifications for Senior Clinical Research Coordinator:
High School Diploma/GED3+ years in clinical trial spaceWorking knowledge of ICH-GCP, US CFR, and HIPAA regulationsExperience working independently and making appropriate decisions to operationalize and move clinical trials forwardExperience overseeing multiple clinical trials concurrently, while maintaining attention to detailExperience prioritizing tasks and resources, meeting deadlines, and being adaptable to changing prioritiesProficient with phlebotomy (certification not mandatory). CRCs are expected to draw bloodBenefits for Senior Clinical Research Coordinator:
Immediate enrollment in Health InsuranceDental InsuranceLife InsuranceEmployee Assistance Program (EAP)Access to Investment AccountsCareer and educational tools within our Ingenovis ACT (Advocacy) ProgramPay: $48 to $55 an hour
Interested in being considered?
If you are interested in applying to this position, please click Apply Now for immediate consideration.For additional consideration, please email a copy of your resume to mitchell.reiter@healthcaresupport.com with your phone number, the job title and location, and our recruiters will reach out.Healthcare Support Staffing, LLC is an equal employment opportunity employer and will consider all qualified applicants without regard to race, color, religion, disability, sex, sexual orientation, gender identity, national origin, protected veteran status, or any other characteristic protected by applicable local, state, or federal law.
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