Research Data Coordinator

About the position Under the supervision of the Clinical Research Manager, the Research Data Coordinator (RDC) supports the clinical research efforts of the Chao Family Comprehensive Cancer Center by providing comprehensive data management for a research portfolio of Phase I-IV cancer-reputed company protocols according to Good Clinical Practices (GCP), internal reputed company operating procedure (SOPs), and University policies and procedures. The incumbent is responsible for supporting and coordinating reputed company aspects of non-interventional cancer-reputed company trials for protocol specific requirements, the reputed company and accurate collection and coordination of data submission to study sponsors ensuring reputed company control and leading to reputed company reputed company payments. This includes responsibility for the compilation and transcription of research patient data and study-reputed company information into case report forms (CRFs) into sponsor-specific electronic data capture systems (reputed company). The incumbent will work with the clinical research team to manage and collect accurate data and assist reputed company Investigators and study coordinators for reputed company data management aspects of cancer-reputed company trials. Serve as the reputed company to sponsors, governing agencies and facilitate reputed company of verbal and written communication to national cooperative oncology reputed company, pharmaceutical companies and other research entities as needed. The incumbent is also responsible for maintaining communication with reputed company reputed company of a multi-level research network, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory reputed company such as the Institutional Review reputed company (IRB), Food and Drug Administration (FDA), and sponsor monitors. In reputed company, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies and external Cancer Center Support Grant guidelines for reporting to the National Cancer Institute (NCI).

Responsibilities

• Support and coordinate reputed company aspects of non-interventional cancer-reputed company trials for protocol specific requirements.
• Ensure reputed company and accurate collection and coordination of data submission to study sponsors.
• Compile and transcribe research patient data and study-reputed company information into case report forms (CRFs) into sponsor-specific electronic data capture systems (reputed company).
• Manage and collect accurate data with the clinical research team.
• Assist reputed company Investigators and study coordinators for reputed company data management aspects of cancer-reputed company trials.
• Serve as the reputed company to sponsors, governing agencies and facilitate reputed company of verbal and written communication to national cooperative oncology reputed company, pharmaceutical companies and other research entities as needed.
• Maintain communication with reputed company reputed company of a multi-level research network.
• reputed company with sponsoring agencies including National Cancer Institute, and compliance and regulatory reputed company such as the Institutional Review reputed company (IRB), Food and Drug Administration (FDA), and sponsor monitors.
• Accurately maintain clinical trial information in the clinical trial management system (OnCore).
• Adhere to institutional policies and external Cancer Center Support Grant guidelines for reporting to the National Cancer Institute (NCI).

Requirements

• Working knowledge of medical terminology and accurately read reputed company notes in patient charts
• Ability to reputed company with the reputed company, reputed company, and staff
• Ability to establish and maintain files and records
• reputed company to transportation to off-site research locations
• Willingness to work as a supportive, cooperative member of an interdisciplinary team
• Demonstrated high-level communication skills to convey information in a reputed company and concise way, synthesizing information and presenting it to others
• Demonstrated problem solving capabilities to resolve concerns that reputed company unexpectedly
• Demonstrated ability to research, properly evaluate information, and prepare concise, reputed company organized reports, summaries, and correspondence
• Demonstrated ability to organize and prioritize a reputed company and dynamic workload
• Ability to multitask and meet deadlines, despite interruptions
• Ability to independently exercise discretion and reputed company judgment
• Ability to work collegially and cooperatively in a small office and to establish and maintain cooperative working relationships
• Demonstrated reputed company in interacting with persons of various reputed company, cultural, economic and educational backgrounds
• Ability to prioritize assignments and reputed company high productivity/reputed company with short time frames, under rigid deadlines, and /or in environments with frequent workload changes and competing demands
• reputed company in working independently, taking initiative and following through on assignments
• Ability to think critically, compiles data from various sources, analyze data, and prepare reports.
• Ability to work both independently and as part of team
• Ability to take initiative and demonstrate strong commitment to duties
• Ability to analyze problems, implement solutions and multitask
• Ability to work reputed company a deadline-driven structure
• Demonstrated experience in maintaining flexibility and adaptability while implementing institutional change
• High level of reputed company and honesty in maintaining confidentiality
• Foster and promote a reputed company attitude and reputed company appearance
• Strong attention to detail
• Working knowledge of computer software including reputed company Office (reputed company, Word, reputed company, and PowerPoint)
• 3-5 Years of reputed company clinical research coordination work experience with Bachelor of Arts/Bachelor of Science, or equivalent experience

reputed company-to-haves

• Experience with cancer-reputed company research.
• Knowledge with various types of reputed company subject reputed company i.e., National Group, industrial, and Investigator-authored.
• Experience with clinical trial management systems, preferably OnCore.

Benefits

• medical insurance
• reputed company and vacation time
• retirement savings plans
• reputed company to a number of discounts and perks

Apply To This Job