Clinical Research Coordinator

Benefits

Qualifications

• •Employee must be available during “core” clinic hours of 8:00 a.m. to 5:00 p.m., Monday through Friday with some flexibility to work from 1-3 hours on Saturday, if needed
• •This is not a remote position as it requires direct patient care in a clinical setting
• •2+ years of Clinical Research experience is required
• •Bachelor’s Degree is required
• •Phlebotomy certification is required
• •Ability to collect patient vitals and ECGs
• •A medical degree is not required
• •Great communication skills, including verbal, written, and personal
• •Proficient in MS Applications
• •Solid data entry skills
• •Capable of multi-tasking in a fast-paced clinic environment
• •Reliable and dependable to finish projects, deliverables, and tasks on time without close supervision
• •Outstanding organizational skills in managing paper and electronic documents
• •10 more items(s)

Responsibilities

• •Complete QC of patient medical records and source documentation
• •Assist in managing all regulatory documents
• •Assist with managing clinical trials, collecting data, informing participants about study objectives, and administering questionnaires
• •Act as a point of contact for sponsors/CROs
• •Facilitate and coordinate monitoring visits
• •Support marketing activities, as needed
• •Maintain clinical research professional credentials
• •4 more items(s)