Clinical Research Coordinator II - Cardiology - Drug & Device Team

MedStar • Washington, DC

132d • $58,656 - $98,384

About The Position

We have an opportunity available for an experienced Clinical Research Coordinator II to join our cardiology drug and device team with MedStar Health Research Institute in Washington, DC. Implements and coordinates research and administrative procedures for the successful management of clinical trials. Performs diverse administrative duties requiring analysis, sound judgment and a high level of knowledge of study specific protocols. Enters study and/or research participant data into the Clinical Trial Management System (CTMS) as applicable. We are unable to offer visa sponsorship for this position. Applicants must be authorized to work in the United States on a full-time, permanent basis without the need for current or future sponsorship.

Requirements

• Bachelor's degree or an allied health or related professional degree, or equivalent work experience.
• 2 years of relevant clinical research experience required.
• Experience in a healthcare setting preferred.
• Undergraduate and/or work experiences that demonstrate aptitude for research facilitation preferred.
• Verbal and written communication skills.
• Basic computer skills preferred.

Responsibilities

• Oversight and/or responsibility for the Institutional Review Board (IRB) submissions and other related regulatory forms.
• Developing informed consent documents and supporting the safety of clinical research participants.
• Explaining the informed consent process and the study to the research participant.
• Developing an effective recruitment plan and recruiting research participants.
• Completing and maintaining case report forms and reviewing data against the research participant's medical record.
• Ensuring proper collection, processing, and shipment of biospecimens and pharmacokinetics.
• Conducting research participant interviews and assessments at study visits.
• Receiving and maintaining test articles from sponsor and inventory test articles.
• Ensuring that non-serious and serious adverse events are properly identified, documented, and reported.
• Understanding and complying with rules for billing Medicare, Medicaid, and third-party payors.
• Returning or disposing of unused supplies per sponsor's requirement during study close-out.
• Acting as a liaison with research participants, investigators, sponsors, and healthcare professionals.

Benefits

• This position has a hiring range of $58,656 - $98,384.

What This Job Offers

• Industry: Administrative and Support Services
• Education Level: Bachelor's degree