Clinical Research

• In collaboration with other members of the clinical research site team, works to support source document requirements for assigned studies.
• Creation of source documents that will follow GCP Guidelines and 21 CFR Part 11 Compliance in addition to internal SOPs.
• Create templates, worksheets, supplemental source for visits based on detailed review of protocol-defined exams, tests, evaluations, and assessments.
• Initial creation of source documents will use all available protocol specific documents (i.e., current IRB approved protocol, blank or annotated CRF, Sponsor provided source templates/worksheets, or reference manuals) to create a source document that is accurate and complete and to ensure that the source document is equipped to record all the required data for the visit.
• Creating, maintaining, updating, control, and release source documents, including paper and electronic source documents in line with the study protocol, and relevant sponsor guiding documents.
• Reviewing draft source and ensuring it is accurate and complete and to ensure that the source document is equipped to record all the required data for the trial.
• Coordinating initial source review and update process.
• Filing, maintaining, distributing, organizing, and archiving source documents for each clinical trial.
• Updating current source documents according to new clinical study protocol amendments.
• Activating studies and visits at the appropriate time.
• Supporting Quality Control (QC) of source documents before it goes to the users.
• Attending all relevant meetings to stay up to date with upcoming studies, progress on current studies, and studies closing out.
• Maintaining a single tracker for the department to track source document design activities and the status of the activities.
• Maintaining version control of all source documents.
• Managing daily communication with site staff and other internal departments.
• Remaining up to date with all assigned Clinical Study Protocol for study.
• Developing and maintaining excellent working relationships with internal and external clients to understand and meet their needs in line with company policies and procedures.
• Maintaining a positive, results-oriented work environment, building partnerships within the team and across the organization at large, and modeling teamwork.
• Participating in continuing education activities to maintain current knowledge of source document design and relevant software.
• Performing all other duties that may be requested or assigned.

Clinical Research Source Development Coordinator

• Join our Clinical Surveillance & Training (CST) team as a Clinical Scientist
• Lead Rater Training Excellence: Design and deliver scientifically grounded rater training programs to ensure consistent, high-quality endpoint assessment and reduce variability across sites
• Drive Patient Eligibility Quality: Perform comprehensive eligibility reviews, providing a second level of scientific oversight to confirm appropriate patient selection and minimize protocol deviations and safety risks
• Deliver Data-Driven Insights: Analyze clinical and endpoint data to identify trends, variability, and potential risks—translating findings into actionable insights that improve study execution
• Shape Protocol Strategy: Partner with sponsors and study teams to review protocols and provide expert guidance on endpoint strategy, scale selection, and study design feasibility
• Act as a Scientific Leader: Collaborate cross-functionally with clinical operations, medical, and sponsor teams to proactively identify risks and deliver solutions that protect study integrity

Clinical Scientist – Clinical Surveillance & Training, Clinical Psychologist/Neuropsychologist

• Develop medical plans and coordinates with Medical Directors
• Perform medical reviews of data listings
• Author and review medical data queries
• Manage project scope and quality of deliverables
• Collaborate with study team members to identify risks

Clinical Scientist – Immunology, Ulcerative Colitis, Crohn’s Disease, Rheumatology

• Provide primary support to investigator-initiated and pharmaceutical research studies
• Assist with data collection, documentation, intake/registration
• Maintain source documents
• Participant recruitment and retention
• Data entry into research systems and data audits
• Research supply inventory maintenance
• Perform administrative tasks and clinical assessments as assigned

Clinical Research Assistant – Cardiometabolic Program

• Reviewing all applicable study documents to complete the Cost and Coverage Analysis
• Completing CCA for all BH research studies utilizing clinical skills, good clinical practices and knowledge of research and government regulations
• Creating study budgets for all research activity occurring within a BH facility
• Ensuring regulatory compliance and financial coverage
• Developing and maintaining effective project relationships
• Evaluating approximately 100 new study proposals per year with a research budget in excess of $3 million

Senior Clinical Research Financial Analyst

• Ability to phone screen patients or caregivers in caring and empathetic manner.
• Document patient information correctly in the computer database.
• Schedule/reschedule patient screen and prescreen appointments.
• Manage incoming calls from patients interested in taking part in research studies.
• Evaluate eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with site clinic staff.
• Learn and maintain knowledge regarding clinical research studies including inclusion and exclusion criteria for different studies.
• Record contact status of patients and document information in the database.
• Review, call and update sponsor patient portals as needed.
• Perform all other duties that may be requested or assigned.

Clinical Research Patient Recruiter

• Review all applicable study documents to complete the Cost and Coverage Analysis
• Ensure analytical evaluations provide relevant and complete measures of cost, revenue, and billing projections and processing
• Ensure regulatory compliance and financial coverage
• Develop and maintain effective project relationships
• Complete Cost and Coverage Analysis for all BH research studies
• Negotiate study budget and assess study financial risk/benefit ratio
• Coordinate closely with Banner Research and University of Arizona staff in the study approval process

• Lead end-to-end clinical trial execution, ensuring delivery against timelines, quality standards, and budget
• Provide operational oversight of site management and monitoring activities, including on-site and centralized monitoring
• Identify, assess, and proactively mitigate clinical and operational risks using a risk-based management approach (RACT)
• Serve as the primary escalation point for CRAs, investigative sites, and cross-functional stakeholders
• Partner closely with Study Start-Up, Data Management, Biostatistics, Safety, and Patient Recruitment teams to drive milestone achievement
• Leverage integrated systems and data (CTMS, EDC, ePRO, TMF, dashboards) to monitor performance, trends, and risk indicators
• Ensure ongoing inspection readiness and compliance with ICH-GCP, SOPs, and global regulatory requirements
• Lead study-specific training and foster alignment across the clinical trial team
• Review metrics and operational data to anticipate challenges and implement timely solutions
• Mentor and support CRAs, contributing to a culture of accountability, continuous improvement, and collaboration

See all jobs on JobTailor

Clinical Research Source Development Coordinator

Clinical Scientist – Clinical Surveillance & Training, Clinical Psychologist/Neuropsychologist

Clinical Scientist – Immunology, Ulcerative Colitis, Crohn’s Disease, Rheumatology

Clinical Research Assistant – Cardiometabolic Program

Senior Clinical Research Financial Analyst

Clinical Research Patient Recruiter

Senior Clinical Research Financial Analyst

Clinical Trial Manager – US