Clinical Research Coordinator

Trinity Health•Central City, IA

2d•Onsite

About The Position

MercyOne is seeking a Research Coordinator for their MercyOne Iowa Heart Center in West Des Moines. This role supports the execution of clinical trials and research studies for adult patients, acting as a resource for each research protocol. The position is in-person within the clinic.

Requirements

Prior patient and clinical research experience
Basic Life Support (BLS) for the Healthcare Provider certified or obtained within three (3) months of hire
Proof of completion of Mandatory Reporter abuse training specific to population served within three (3) months of hire
High-school diploma required
Basic Computer proficiency (e.g., Microsoft office, data entry systems)
Excellent communication and interpersonal skills
Valid Iowa Driver’s/Chauffeurs License required, must meet Mercy’s Motor Vehicle Safety Standards, must be at least 18 years of age and be eligible to drive per Iowa state law
Three years of paramedic experience recommended for paramedic candidates
Two years of critical care experience preferred or clinical cardiac equivalent experience preferred

Nice To Haves

Bachelor of Science (e.g., biology, health sciences)
Medical assistant, LPN, and/or Paramedic certification
Clinical Healthcare experience in cardiology or research
Ability to manage multiple tasks and meet deadlines
Knowledge of medical terminology

Responsibilities

Coordinate and manage day-to-day clinical trial activities
Recruit, screen, and enroll study participants according to study protocol criteria
Obtain informed consent and ensure participant understanding of study procedures
Coordinate, schedule, and conduct study visits, including follow-up visits
Collect, record, and maintain accurate study data and source documentation
Organize and assist with site visits by protocol sponsors monitoring CRAs (clinical research associates)
Participate in professional development activities and maintain professional affiliation and certification as per licensure requirements
Monitor patient safety and report adverse events as required
Complete necessary correspondence with drug company and IRB
Maintain inventory of study supplies and IP - (study product/device/drugs)
Ensure compliance with Good Clinical Practice (GCP), institution policies, and federal regulations
Complete necessary paperwork and electronic data collection for research studies
Assist in preparation of information for submission to Institutional Review Board (IRB) for approval
Travel to Iowa Heart offices as needed