Clinical Research Coordinator at Urology of Virginia PLLC

Virginia Beach, Virginia, United States -

Full Time

Start Date

Immediate

Expiry Date

09 Oct, 26

Salary

0.0

Posted On

11 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research Coordination, Good Clinical Practice (GCP), FDA Regulations, Data Management, Technical Protocol Analysis, Interpersonal Communication, Patient Interaction, Quality Control, Clinical Monitoring, Administrative Support

Industry

Medical Practices

Description

Description Company Overview Urology of Virginia (UVA) has a long history of providing comprehensive and quality care to the entire Hampton Roads region, including northeastern North Carolina. Our clinical care team consists of board-certified urologists, most of whom are fellowship-trained, nationally recognized, awarded, and published. Working in a team-based environment, our mission is to help patients optimize their urological health. Job Overview We are seeking a Clinical Research Coordinator to conduct clinical trials according to Good Clinical Practice (GCP) and FDA regulations. Duties and Responsibilities Employee Core Values: People First – Delivers exceptional customer service by putting patients first, approaching challenges with a problem-solving mindset, and consistently demonstrating professionalism, compassion, and respect for everyone. Be Accountable – Consistently reliable and hard-working, demonstrating strong accountability and deep commitment to achieving responsibilities and goals. We Before Me – Collaborative team player who steps in to help first and actively encourages teamwork to achieve shared goals. Pursue Excellence – Expects, projects, and demonstrates excellence through consistent attention to detail in everything they do. Communicate Well – Consistently delivers clear, concise, and professional communication across all interactions. Primary: Coordinates and implements approved research studies according to the study protocol and the policies of Urology of Virginia Research Documents and maintains data for all study related procedures, processes, and events Participates in study related meetings (out of state travel), quality control, monitoring visits and audits Performs selected administrative duties delegated by Director of Research or principal investigators Requirements Able to read, analyze, and interpret information from technical and scientific protocols and government regulations Possess excellent verbal and written communication skills as well as excellent interpersonal skills Able to effectively present information and respond to questions from physicians, staff, and patients. Graduate of either an accredited Medical Assistant /Medical Technologist program, accredited school of professional nursing or possess a Bachelor’s Degree Minimum of 2 years’ experience in clinical research or in a clinical office setting (urology preferred) Certification by ACRP or SOCRA may be considered in place of education requirements Equal employment opportunity for all is a very important philosophy for our practice. We will evaluate all applicants and employees without regard to race, color, religion, national origin, sex, age, non-disqualifying disability, history of military service, genetic information, or any other status protected by law. This policy applies to all employment practices, including, but not limited to, recruitment, employment, assignments, promotions, reassignments or

Responsibilities

Coordinates and implements approved research studies according to study protocols and company policies. Manages research documentation, data, and participates in monitoring visits and audits.