Clinical Research Coordinator - Southfield, MI

IQVIA; Parsippany-Troy Hills (NJ); Presencial; USD 48 000 - 58 000; Tempo integral

Resumo da oferta

IQVIA is seeking a Clinical Research Coordinator to join our on-site team in Southfield, MI. You will perform clinical procedures, recruit and screen patients, and ensure adherence to study protocols and GCP guidelines.

Responsibilities include coordinating studies, maintaining data integrity in CRFs/EDC, and supporting investigators and monitors to deliver high-quality results while prioritizing patient safety and compliance.

Qualificações

• Bachelor’s degree preferred or equivalent combination of education and relevant experience.
• Minimum 1+ years of relevant work experience in clinical research.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Experience conducting patient study visits and participant-facing clinical research activities.
• Demonstrated ability to recruit and screen patients according to study eligibility criteria.
• Proficiency with EDC systems, including accurate data entry, query resolution, and data management processes.
• Strong attention to detail and ability to establish effective working relationships.

Responsabilidades

• Perform ECGs, sample collection, and vital signs assessments.
• Coordinate clinical research studies and maintain compliance with study protocols and GCP guidelines.
• Conduct patient study visits and support participants throughout the research process.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, evaluating eligibility based on criteria while ensuring safety.
• Collect, enter, and maintain accurate clinical data in CRFs and EDC systems.
• Assist with EDC query management and resolution, ensuring data accuracy and quality.
• Collaborate with investigators, sponsors, and monitors to address study-related issues.
• Act as a patient advocate and maintain a safe environment per Health and Safety policies.

Conhecimentos

Clinical research experience

GCP knowledge

Patient visits

EDC proficiency

Data integrity

Formação académica

Bachelor’s degree or equivalent

Ferramentas

EDC software

Descrição da oferta de emprego

Clinical Research Coordinator - Southfield, MI Work Set-Up: On-site Schedule Weekly Hours: 40 hours/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 the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

About the Role

We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands‑on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.

Key Responsibilities

• Perform a variety of clinical procedures, including ECGs, sample collection, and vital signs assessments.
• Coordinate clinical research studies and maintain compliance with study protocols and Good Clinical Practice (GCP) guidelines.
• Conduct patient study visits and support participants throughout the research process, ensuring a positive study experience.
• Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
• Recruit, screen, and orient patients, evaluating eligibility based on study inclusion and exclusion criteria while ensuring their safety and well‑being throughout the study.
• Collect, enter, and maintain accurate clinical data in case report forms (CRFs) and Electronic Data Capture (EDC) systems.
• Assist with EDC query management and resolution, working closely with investigators and monitors to ensure data accuracy, completeness, and quality.
• Collaborate with investigators, sponsors, and study monitors to address study‑related issues and maintain high standards of data integrity.
• Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Qualifications

• Bachelor’s degree preferred or equivalent combination of education and relevant experience.
• Minimum 1+ years of relevant work experience in clinical research.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Experience conducting patient study visits and participant‑facing clinical research activities.
• Demonstrated ability to recruit and screen patients according to study eligibility criteria.
• Proficiency with EDC systems, including accurate data entry, query resolution, and data management processes.
• Strong attention to detail and ability to establish effective working relationships.

Please note: This position is not eligible for sponsorship.

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.

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 https://jobs.iqvia.com

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.

IQVIA 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.