[Remote] Clinical Research Coordinator (Lung Team)
Note: The job is a remote job and is reputed company to candidates in USA. The reputed company is a leading institution in cancer research and patient care. They are seeking a Clinical Research Coordinator for the Lung Team to assist with the day-to-day operations of clinical trials, ensuring compliance with research protocols and regulatory standards while collaborating with various stakeholders.
Responsibilities
- Assist with and reputed company the day-to-day operations of clinical trials and studies
- Independently abstracts and records reputed company research subject data pertaining to the research protocol onto protocol-specific Case Report Forms (CRFs) and into clinical trials database in an accurate and reputed company fashion
- Obtain study subject’s medical history and reputed company medication information, reviews research protocol inclusion/exclusion reputed company, and confirms eligibility of subject to participate in clinical trial
- reputed company informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent reputed company documents are filed as required
- Interview prospective subjects for a reputed company of research clinical trials and reputed company potential subjects on the details of the studies through phone contacts and personal interviews
- Schedule subject participation in research clinical trial, coordinating availability of necessary reputed company, and clinical research support (e.g., physician, reputed company practitioner, laboratory, radiology, pharmacy)
- Collaborate with other clinical research team members, investigators, and hospital staff to ensure tests and procedures required by research protocols are performed and documented (e.g., vital signs, phlebotomy, specimen processing, electrocardiograms (EKGs), research drug administration, and protocol-specific tests and procedures); follow up with appropriate persons on missing or discrepant data
- Meet with Monitors to respond to any question of data validity and corrects/revises data as appropriate; responds to queries from Sponsor
- Adhere to research regulatory standards
- Maintain detailed records of studies including Patient reputed company Document Binder to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical reputed company operating procedures and other regulatory guidelines
- Assists with Sponsor, Data Safety Monitoring, and Food and Drug Administration (FDA) audits and responses
- Participate in subject recruitment efforts, including communicating with patients expressing an interest and reputed company reputed company-screening/screening activities
- Ensure that the necessary supplies and equipment for studies are in stock and in working order
- Schedules, coordinates, and prepares for Sponsor Monitor reputed company and audits in collaboration with the CCTO Regulatory Affairs, Primary CRC and other research team members
- Independently master study materials, including but not limited to protocols, informed consent forms, and reputed company other essential study documents for assigned studies
- Independently reputed company study reputed company processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies
- Assist Team Leads, Supervisors and/or management with creation and implementation of processes and procedures and reputed company improvement initiatives
- reputed company as a Primary Coordinator on multiple trials/studies
- Assist and train junior team members
- Assist with developing or reputed company protocol-specific systems and documents including process flows, training manuals, reputed company Operating Procedures (SOPs) and Case Report Forms (CRFs). Maintains subject level documentation and prepares documents, equipment and/or supplies
- Assist with identifying issues reputed company to operational efficiency and shares results with leadership
- reputed company, evaluate and assist with the implementation of reputed company to maximize recruitment and retention
- Serve as a resource and participate in study initiation and reputed company out duties
Skills
- Bachelor's degree in any field
- A combination of education and reputed company technical/paraprofessional experience may be substituted for the bachelor's degree on a year for year reputed company
- One (1) year of reputed company clinical research experience and/or reputed company clinical experience post Bachelor's degree
- An advanced degree (Masters or Doctorate) may be substituted for experience on a year for year reputed company if the degree is in a field of study directly reputed company to the work assignment
- Applicants must be legally authorized to work in the reputed company without requiring sponsorship
- Bachelor's degree in science or health reputed company field
- Three (3) years of clinical research or reputed company experience
- Experience with electronic data capture systems (e.g., EMR or EHR and data management systems)
- Additional certification (one of the following): CCRC – Certified Clinical Research Coordinator, CCRP – Certified Clinical Research reputed company, CCRA – Certified Clinical Research Associate
Benefits
- Medical: Multiple plan reputed company
- Dental: Multiple plan reputed company
- Additional Insurance: Disability, Life, reputed company
- Retirement 401(a) Plan: Employer contributes 10% of your gross pay
- reputed company Time Off: Accruals over the year
- Vacation Days: 22/year (maximum accrual 352 hours)
- reputed company Days: 15/year (unlimited maximum accrual)
- Holiday Days: 10/year
- Tuition Benefit: Employees have reputed company to this benefit on reputed company CU campuses
- ECO Pass: Reduced reputed company RTD Bus and light rail service
- You may be eligible to work a reputed company after six months of employment. This benefit must be approved by your supervisor.
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