Research Assistant - Medical Assistant

New Yesterday

Position Overview--The role of the Clinical Research Assistant is to perform a wide variety of clinical and administrative tasks to assist the clinical research coordinator in conducting clinical trials. The research assistant is responsible for study support activities to ensure each study is completed accurately, according to protocol, and on time. --To consistently embody AMR's Core Values:--Excellence and ConsistencyCollaborative InnovationRespect for our Subjects, Sponsors and Team MembersCommunityUnimpeachable EthicsThe Clinical Research Assistant reports to the Team Lead/Site Manager/General Manager.--Classification: Non-Exempt--Primary Responsibilities:--Assist coordinators with administrative study activities in a timely manner as necessary.Assist monitor during all site visits if applicable.Maintain accurate enrollment/drug logs if applicable.Assist in general office workflow which includes telephone answering.Responsible for assisting regulatory administration work for necessary periodic IRB reviews, both ongoing and final.Establish and maintain patient rapport during clinical drug trials to include management of subjectsClinical data collection such as vital signs, EKG recording, subject weightsMedical record retrieval and review when requiredSubject interviewsPhlebotomySpecimen collection, processing, and storageComplete source documentationFiling and pulling study recordsTransporting clinical specimens to the laboratoryAnswering and triage of research office callsWork with physicians and other staff to maintain a more effective and systematic method to investigate clinical problems related to the support of the clinical trial patients.Facilitate communication between the site and various monitors, to include telephone and written correspondence as well as monitoring visits.Scheduling of various visits/procedures--Assists providers with various visits/procedures--Perform site and protocol specific training in a timely mannerOther duties as assigned----Additional Responsibilities (Check If Applicable):-- Cross train in lab coordinator duties to serve as a backup.-- Monitor patient arrivals and check-in subjects according to receptionist duties-- Responsible for filing source documents in the subjects charts-- Take patient history-- Train subjects on diaries-- Create screening charts once the screen source is available-- All screening chats and randomization charts for the next day pulled-- Clinic rooms and subject bathrooms are stocked including necessary medical supplies----Desired Skills and Qualifications:--At least 6 months of past medical office experience, medical certificate, or equivalent previous work experience required.--Phlebotomy skills preferredAbility to work consistently and effectively as part of a high-performance work team.Ability to effectively devote keen and acute attention to detail.--Demonstrated ability to exercise standard Universal Precautions, or ability to quickly learn and apply Universal Precautions.--Positive attitude and the ability and desire to work in a company that embraces collaboration and a team approach.--Demonstrated ability to operate basic office equipment including (but not limited to) copy machines, facsimile machine and computers.Strong verbal and interpersonal skills--Professional and highly motivated "self-starter" with the ability to exercise initiative, together with ability to work as a team player as well as independently while managing a variety of skills in a variety of software environments, i.e., Word, Excel, Internet.Excellent task management and prioritization skills.Proven ability to successfully build and cultivate excellent long-term relationships--Excellent follow up--AMR Clinical does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non-merit factor.----** This job description is intended to be a representative summary of the major responsibilities and accountabilities of the staff holding this position. The staff may be requested to perform job-related tasks other than those stated in this description.--Compensation details: 23-27 Hourly WagePI3089c0c94021-25660-38135817
Location:
Oak Brook, IL, United States

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