Medical Assistant to function in a clinical research role

Mid-Atlantic Nephrology Associates PA•Catonsville, MD

9d•Onsite

About The Position

Large nephrology practice in Baltimore seeks a Medical Assistant to function in a clinical research role to be responsible for coordination of all aspects of assigned clinical trials from pre-study planning through successful completion of all patient/subject visits and study documentation; directly involved in patient/subject care and study subject’s procedures and activities. The Medical Assistant to function in a clinical research role for the nephrology practice is responsible for overseeing all aspects of clinical research studies, ensuring compliance with regulatory standards, and facilitating the conduct of the study.

Requirements

Must be proficient with computers, Microsoft Office applications and Windows operating systems.
Ability to communicate and maintain effective interpersonal relations at various levels of the organization.
Strong organizational and communication skills
High School diploma or graduation equivalent.
Prospective employees must pass a criminal background check and provide proof of Influenza Vaccination including booster.

Nice To Haves

1-year of related experience preferred.
1-2 years of clinical trials/research experience are preferred.

Responsibilities

Collect study data by recruiting and coordinating activities of study participants.
Utilize a basic understanding of the clinical study background and rationale to explain the study to potential and current participants.
Responsible for patient enrollment, verify patient conformity to inclusion/exclusion criteria prior to patient enrollment in the study.
Assist in developing recruitment strategies for one or more studies.
Maintains detailed knowledge and understanding of assigned protocols, including all protocol requirements for patient/subject visits, obtaining informed consent, visit schedules, tests, procedures, laboratory information, and drug accountability requirements.
Set up tools and procedures for data collection and study processes.
Perform data entry and organize data in approved systems.
Serve as liaison between study team and IRB for routine administrative matters.
Prepare routine reports related to study accrual, study trends, efficiency-related issues.
Contact participants to confirm, schedule, and retain.
Responsible for all study documentation forms.
Other duties as assigned.