Research Coord Associate- Lutheran General
3 weeks ago
Department:
80028 Research - Clinical Trials: OncologyStatus:
Full timeBenefits Eligible:
YesHou rs Per Week:
40Schedule Details/Additional Information:
Hybrid (onsite/remote) Monday through Friday
Not a full remote position. Must be able to work a hybrid schedule.
Major Responsibilities: Assists in screening for research trials/projects and gathers patient information from medical record in order to complete case report forms and resolve queries.Reviews patient medical records, database records, and other sources to screen and identify potential subjects for inclusion in research protocols/projects. Obtains patient consent, registers the patient, and submits data as required. Maintains confidential materials and records.Enters and maintains patient and study information in electronic systems.Maintains accurate records of the receipt, inventory and distribution of research materials (i.e. lab kits, study specific supplies, dry ice, and office supplies.)Facilitates the collection, processing, and tracking of submission of research specimens according to protocol/project requirements to the appropriate location.Collaborates with sponsors to schedule and facilitate study related visits.Other duties as assigned by the AARI Manager.Develops understanding of Good Clinic Practice and International Conference on Harmonization Guidelines, Federal Code of Regulations, FDA Guidance, Institutional and AAH policies and departmental SOPs.Licensure, Registration, and/or Certification Required: None Required.
Education Required: Associate's Degree (or equivalent knowledge) in Health Science or related field.
Experience Required: Typically requires 1 year of experience in Research or prior healthcare preferred.
Knowledge, Skills & Abilities Required: Medical terminology.Good understanding of computer software, Microsoft Office, Word, Excel and Teams.Excellent communication and organizational skills and the ability to work within a team environment.Ability to understand and communicate research protocol requirements to others.Ability to work independently with a high degree of accuracy and attention to detail.
Physical Requirements and Working Conditions: Must be able to sit, stand, walk, lift, squat, bend, reach above shoulders and twist throughout shift.Must have functional sight and hearing.Ability to function in a latex environment.May be exposed to mechanical, electrical, chemical, and radiation hazards as well as blood and body fluids on a continuous basis; therefore, protective clothing (i.e., gown, mask, goggles, gloves, etc.) must be worn as necessary.Exposed to a normal office environment.Operates all equipment necessary to perform the job.Position may require travel among sites and therefore there is exposure to road and weather conditions.
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