Clinical Research Coordinator Albuquerque, NM
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Job Location:
Parsippany, NJ - USA
Hourly Salary:
$ 35 - 42
Posted on:
4 hours ago
Vacancies:
1 Vacancy
Job Summary
Clinical Research Coordinator - Albuquerque NM
Work SetUp: Onsite
Schedule: Up to 40 hours per week (Parttime)
About IQVIA
IQVIA is a global leader in advanced analytics technology solutions and clinical research services. We collaborate with leading pharmaceutical biotechnology and medical device organizations to advance innovation and improve patient outcomes worldwide. Through scientific expertise operational excellence and cuttingedge technology IQVIA is shaping the future of healthcare.
About the Role
IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This role is wellsuited for a detailoriented research professional who enjoys direct patient interaction values data integrity and is committed to highquality clinical research within diverse communities.
As a CRC you will play a critical role in coordinating study operations supporting patient recruitment and retention performing studyrelated procedures and ensuring adherence to study protocols and regulatory requirements.
Key Responsibilities
Coordinate and conduct clinical research activities in accordance with study protocols Good Clinical Practice (GCP) and applicable regulatory requirements
Perform studyrelated clinical procedures including ECGs vital signs and biological sample collection
Conduct patient visits including screening enrollment education orientation and followup
Support patient recruitment efforts and community outreach including bilingual (English/Spanish) communication
Prepare study materials manage equipment setup and support daily clinic operations
Accurately collect document and enter clinical data into electronic data capture (EDC) systems and case report forms (CRFs)
Request review and manage medical records to support study eligibility and documentation
Collaborate with investigators sponsors and monitors to address data queries and ensure study quality
Maintain a safe clinical environment and serve as a patient advocate throughout study participation
Qualifications
Bachelors degree preferred or an equivalent combination of education and relevant experience
Minimum of 1 year of clinical research coordination experience including prior study coordination
Handson experience with clinical research operations including:
Data entry and query resolution in EDC systems
Chart prescreening and patient prescreening activities
Conducting and coordinating patient visits
Patient outreach and education via phone and facetoface communication regarding clinical trials
Scheduling study visits and managing visit logistics
Collection processing and shipping of laboratory samples
Recruitment activities and participant followup
Regulatory document review and maintenance
Working knowledge of clinical trial processes GCP guidelines and medical terminology
Experience requesting and managing medical records
Bilingual in English and Spanish (written and verbal) is preferred but not required
Strong organizational skills attention to detail and ability to work effectively with diverse teams and patient populations
Ready to Make an Impact
Join IQVIA and contribute to highquality clinical research that advances science while serving diverse patient communities.
Apply today and be part of a team helping bring innovative treatments to patients.
Additional Information
This position is not eligible for visa sponsorship
#LI-CES #LI-DNP #LI-HCP #ONSITE
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
