Clinical Research Coordinator - Cancer Genetics

Primary Duties And Responsibilities

• Responsible for participant recruitment, data reporting and management, collection of source documents, use and development of case report forms, adverse event reporting, filing and archiving of study records, and resolution of data queries
• Interact with study participants as directed/required by the protocol and/or study team
• Ensure all study related samples are collected, properly prepared and shipped according to the protocol requirements and IATA/DOT regulations
• Coordinate and manage studies, including communication with regulatory authorities
• Closure of studies, including contributing to research articles, audit preparation, and communication with regulatory agencies and other disciplines involved
• Facilitation of blood and tissue specimen collection processes, with potential travel needed to other local institutions via shuttle network. Training and supervision will be provided

Knowledge, Skills, And Abilities Required

• Excellent interpersonal skills and the ability to communicate and relate effectively with diverse groups of patients, medical personnel, and research staff in-person and/or remotely via telephone, e-mail, and videoconferencing
• Detail-oriented with excellent organizational, communication, problem-solving, and time management skills
• Strong computer skills, including proficiency with Microsoft Office products, knowledge or ability to learn other systems such as Epic and REDCap
• Knowledge or ability to learn study data entry and/or CRF completion, research study coordination, and regulatory requirements
• Dependable, motivated, and willing to learn new processes and procedures as needed
• Able to work on-site or remotely, as needed

Supervisory Responsibilities

None

Patient Contact

Will have contact with patients of all ages and populations.

Pay

$48,100.00 - $54,400.00