Clinical Research Coordinator

Adult Pediatric Urology & Urogynecology is hiring a Clinical Research Coordinator to coordinate clinical research studies, including participant recruitment, screening, and enrollment. The role manages study visits, consent, data and regulatory documentation, compliance, collaboration, monitoring and audit preparation, reporting, and study closeout.

Responsibilities

This position is responsible for coordinating clinical research studies, including participant recruitment, screening, and enrollment according to established protocols

The role involves managing study visits, obtaining and documenting informed consent, collecting and entering data, maintaining regulatory binders, and ensuring adherence to Good Clinical Practice and institutional policies

The coordinator will collaborate with physicians, research staff, and external partners, prepare materials for monitoring and audits, and assist with reporting and study closeout activities

Preferred

Hands-on Clinical Research Experience, preferably in urology or related specialties, with exposure to clinical trial workflow

Registered Nurse or LPN license or other healthcare related field experience preferred

Two years in a clinical research setting, preferably working as a clinical research coordinator on Industry-Sponsored clinical trials

Urology experience, preferred not required

Two years of related work experience, preferred; or equivalent combination of experience and education

Two years of related work experience, preferred; or equivalent combination of experience and education.

Clinical research experience

Clinical trial workflow

Urology experience

Registered Nurse (RN) license

Licensed Practical Nurse (LPN) license

Healthcare experience

Clinical research coordination

Industry-sponsored clinical trials

Company

Adult Pediatric Urology & Urogynecology works to treat urological disorders in both adults and children.

Omaha, Nebraska, USA

https://adultpediatricuro.com/

Founded in 1994

11-50 employees

Qualifications

Ability to manage informed consent processes and ensure participants' rights and safety, with demonstrated skill in Informed Consent and participant education

Experience working with study protocols, including implementing Protocol requirements and maintaining protocol compliance throughout the trial

Background in research methodology and study operations, including Research skills and data collection/management practices

Knowledge of Clinical Trials, including trial phases, regulatory requirements, and Good Clinical Practice (GCP) guidelines

Associate or bachelor's degree in a health-related field (e.g., Nursing, Life Sciences, Allied Health) or equivalent clinical research experience

Strong organizational skills, attention to detail, and ability to manage multiple studies and timelines in a fast-paced clinical environment

Effective written and verbal communication skills, with the ability to interact professionally with patients, families, and multidisciplinary teams

Proficiency in electronic medical record systems and basic computer applications for data entry and documentation

CPR

Medication Aide

Hands-on Clinical Research Experience, preferably in urology or related specialties, with exposure to clinical trial workflow

Registered Nurse or LPN license or other healthcare related field experience preferred

Two years in a clinical research setting, preferably working as a clinical research coordinator on Industry-Sponsored clinical trials

Urology experience, preferred not required

Two years of related work experience, preferred; or equivalent combination of experience and education

Required skills

Clinical Research, Clinical Trials, Clinical Practice (GCP), Informed Consent, Protocol Compliance, Research Methodology, Data Collection and Management, Industry-Sponsored Clinical Trials, Urology, Registered Nurse (RN) License, Licensed Practical Nurse (LPN) License, CPR, Medication Aide

Preferred skills

Urology experience, preferred not required, Omaha, Nebraska, USA, https://adultpediatricuro.com, Company data provided by, AI Tools, Customize Your Resume, Maximize your interview chances, Build Cover Letter, Make your application stand out, Analyze How Well You Fit, Understand your strength & weakness

Experience

2+ years