Clinical Research Coordinator Wichita, KS
Job Location:
Parsippany, NJ - USA
Hourly Salary:
Posted:
Application Deadline:
Vacancies:
Job Summary
Work Set-Up: On-site
Schedule: Part-time 24 hours per week
About IQVIA
IQVIA is a global leader in advanced analytics technology solutions and clinical research services dedicated to driving healthcare forward. We partner with leading pharmaceutical biotechnology and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with advanced technology we deliver high-quality insights and support that help shape the future of clinical research.
About the Role
IQVIA is seeking a Clinical Research Coordinator (CRC) to support the successful execution of clinical research studies under the guidance of the Principal Investigator. This role is ideal for candidates with hands-on clinical research experience who are passionate about patient care data quality and advancing healthcare innovation.
The CRC will play a critical role in study coordination patient engagement clinical procedures and data management while ensuring compliance with study protocols regulatory requirements and Good Clinical Practice (GCP) guidelines.
Key Responsibilities
Perform clinical procedures including ECGs vital signs specimen/sample collection and other protocol-required activities.
Coordinate and support daily clinical trial activities in compliance with study protocols GCP and site procedures.
Conduct patient chart reviews and prescreening activities to identify potentially eligible participants.
Recruit screen schedule and orient study participants while ensuring patient safety and a positive participant experience.
Support patient visits and assist with study-related documentation and follow-up activities.
Prepare study materials maintain study supplies and assist with equipment setup and logistical planning.
Collect review and accurately document clinical data in Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems.
Support EDC data entry query resolution and data quality review in collaboration with investigators sponsors and monitors.
Respond to sponsor and monitor queries in a timely and accurate manner.
Maintain confidentiality regulatory compliance and adherence to Health & Safety policies.
Act as a patient advocate and contribute to a collaborative and professional research environment.
Qualifications
Bachelors degree preferred or an equivalent combination of education and relevant experience.
Minimum of 1 years of relevant clinical research experience.
Working knowledge of clinical trials GCP guidelines and medical terminology.
Experience with patient chart review and prescreening activities.
Ability to support patient visits and study coordination activities in a clinical research environment.
Experience with EDC systems including data entry and query resolution.
Strong attention to detail with excellent organizational and communication skills.
Ability to build effective working relationships with patients investigators sponsors and team members.
Please Note
This position is not eligible for sponsorship.
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and/or schedule (full or part-time). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and welfare and/or other benefits.Required Experience:
IC
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
