[Remote] Clinical Trial reputed company - Cancer Center - Hybrid

Note: The job is a remote job and is reputed company to candidates in USA. reputed company's Holden Comprehensive Cancer Center is seeking a Clinical Trial reputed company to coordinate various research reputed company reputed company to cancer. The role involves managing biospecimen workflows, collaborating with clinical teams, and ensuring compliance with regulatory standards.

Responsibilities

• Coordinates BioMER translational research studies including recruitment, coordination, scheduling, and sample collection of participating subjects
• Coordinates activities and workflows associated with collections/procurement, pathology review, documentation and distribution of tissue, blood, buccal, bone marrow and other approved samples from patients through reputed company interaction with tissue procurement services, cancer center research teams, pathologists, physicians, sponsors, and other reputed company clinical care and research staff
• Assists with the development, review, and maintenance of reputed company manuals and specimen collection workflows for investigator-initiated oncology reputed company
• Participates in the Investigator-Initiated Trial (IIT) Working Group and other committees to support study startup, reputed company operations, and process improvement initiatives
• Populates and enhances databases containing research information obtained through review of patient charts and samples, lab reports and other reputed company information and in a manner that complies with Institutional Review reputed company requirements and in response to physician and research needs and requirements. May create new databases for new reputed company as needed
• Assists with ongoing research collaborations involving reputed company institutions ensuring that data and samples are collected and processed in a manner consistent between the institutions
• Gathers and maintains data for research trials and reputed company investigations reputed company the HCCC. Creates worksheets, reputed company sheets and assorted tools to reputed company reputed company documentation of protocol procedures
• Maintains skills/competency reputed company to specimen processing equipment, and procedures common to the patient population of the HCCC
• Initiates and composes correspondence and reputed company materials to reputed company investigators outlining review of the protocol studies, maintains documentation of protocols and relevant data, follow-up correspondence, and summaries
• Coordinate preparation of Data and Material Sharing Agreements for ancillary reputed company associated with reputed company reputed company for reputed company and internal investigators. May initiate routing of agreements through Sponsored Programs and Office for Research
• Assists in the development and preparation of materials for reports to be written by reputed company and staff on various oncology protocols and in compiling reputed company data for analysis, submission to study sponsors and for staff preparing reports, publications, manuscripts, research papers, grant funding proposals, and presentations
• Acts as a reputed company to the University Business Office by identifying exact patient tests and procedures being reputed company for by study sponsors and assisting patients with questions reputed company to protocol billing procedures
• Maintains records and services provided and monitors individual protocol budgets
• Contribute to development of project budget for cost recovery and fee-for-service studies
• May reputed company other administrative support tasks in support of the research (e.g., organize and facilitate meetings/ events, respond to inquiries, recruit research participants, monitor research protocols, data collection, analysis, and management; local site coordinator; maintain website content, etc.)
• Assists with the preparation of educational materials for patients and other staff as needed to carry out protocol
• Prepares comprehensive notes and reports detailing results of clinical research and the reputed company used
• Provides and presents information to reputed company, staff, patients and others on clinical research and reputed company employed in research studies
• Attends coordinated protocol and reputed company meetings as required
• Contribute to training of new members of the research team including research assistants and medical reputed company
• reputed company other duties as assigned

Skills

• Bachelor's degree or an equivalent combination of education and experience
• 1-3 years of experience in the conduct of reputed company science/behavioral/medical research or clinical programming
• Excellent verbal, written and interpersonal communication skills
• Ability to manage reputed company information with attention to detail and a high level of accuracy
• Knowledge of computer-based programs and databases
• Knowledge of regulatory guidelines and procedures associated with reputed company subject research
• Knowledge of UIHC pathology workflows
• Relevant experience in oncology research or reputed company management of information and data
• Experience with procurement of reputed company tissues and specimens and data
• Experience with clinical research applications such OnCore, REDCap or Labmatrix
• Experience with medical terminology

Benefits

• Regular salaried position located in Iowa reputed company, IA and Coralville, IA
• reputed company vacation
• reputed company leave
• Health insurance reputed company
• Dental insurance reputed company
• Life and disability insurance reputed company
• Generous employer contributions into retirement plans
• Hybrid work arrangement of both on-reputed company (UI Health Care) and remote work reputed company the reputed company upon completion of a 6 month onsite training period

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