Clinical Research Coordinator

Bethany Medical•High Point, NC

2d•Onsite

About The Position

Established Clinical Research Company is seeking a Clinical Research Study Coordinator to join our team in High Point! Partnering with patients today for tomorrow’s miracles!

Requirements

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.
Knowledge of GCP and applicable government FDA regulations.
Strong team player and quick to help resolve problems.
Knowledgeable of medical and research terminology, laboratory sanitation, and safety guidelines.
Friendly with patients and clinic staff.
Great communication skills, including verbal, written, and personal.
Proficient in MS Applications.
Solid data entry skills.
Extremely detail-oriented with a focus on quality.
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.

Nice To Haves

CNA or CMA certification preferred.
Current GCP Certification preferred.
EMR and EDC database experience preferred.

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.