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Related keywords
- Clinical Research Manager
- Clinical Research Administrator
- Research Clinical Coordinator
- Clinical Research Supervisor
- Clinical Research Project Manager
- Director Clinical Research
- Clinical Research Intern
- Clinical Research Program Manager
- Clinical Research Data Manager
- Clinical Research Quality Manager
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Clinical Coordinator Jobs
Recruited by The US Oncology Network 9 months ago
Address Germantown, KY, United States
Clinical Research Manager (Hybrid)
Company | Elligo Health Research |
Address | Paducah, KY, United States |
Employment type | FULL_TIME |
Salary | |
Category | Transportation, Logistics, Supply Chain and Storage |
Expires | 2023-06-02 |
Posted at | 1 year ago |
Elligo Health Research is partnering with Aledade to find qualified candidates.
- Manage multiple concurrent trials
- Comply with Aledade, Clinic, Sponsor, and partner policies, standard operating procedures (SOPs) and guidelines
- Collect and provide all documents required for research-related regulatory purposes
- Assist with the screening, recruiting and enrollment of research subjects
- Collect and maintains source documentation
- Serve as the primary contact for clinical trials across the ACO to ensure appropriate communications, trial management, and meeting of timelines
- Coordinate and conduct the informed consent process
- Work closely with Aledade, practice leadership, and other partners to refine clinical trial approaches and identify strategies to bring clinical research as part of care to other Aledade markets
- Ensure all research-required equipment is appropriately calibrated
- Coordinate protocol related research procedures, study visits, and follow-up
- Perform data entry and query resolution
- Working closely with partners on all areas of clinical trials including start-up, vendor management, subject recruitment, protocol training, data entry, and reporting in compliance with sponsor requirements
- Develop strong working relationships and maintain effective communication with study team members and key stakeholders
- Maintain all trial-related training records as required
- Adhere to an IRB approved protocol
- Facilitate pre-study, site qualification, study initiation, monitoring visits, and study close out activities
- Complete all protocol related training
- Order supportive study supplies (e.g., contracts, IXRS, lab kits, nonclinical supply materials, imaging and laboratory handling manuals, etc.)
- Other duties as assigned
- Perform patient/research participant scheduling
- Collect patient/research participant history
- Communicate with internal teams, investigators, ACO board, and stakeholders
- Support the collection and review of required essential study documents and reports
- Support the safety of research subjects, report adverse events
- Collect, process and ship laboratory specimens
- Extensive knowledge of clinical research studies, protocols, etc.
- BS/BA in Life Sciences or related discipline
- Thinks beyond their immediate team and contributes to making Aledade holistically better (active engagement in D&I efforts, culture initiatives, facilitating training, leading roundtables, etc.)
- 5+ years of clinical research coordinator experience
- Exceptional interpersonal skills, the ability to work independently
- Previous GCP training and certification
- Self starter with the ability to run with things
- Demonstrated proficiency with word processing, spreadsheet, database, and presentation software
- Strong verbal and written communication skills
- Ability to travel for clinical activities, attend investigator meetings or vendor visits/audits, as required
- Demonstrated ability to build strong teams and relationships
- Preferred: Nursing experience in a clinical setting
- Strong organizational/prioritization skills for the management of multiple concurrent projects
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