Clinical Research Coordinator - Novi, MI

IQVIA Inc; Novi (MI); Sur place; USD 48 000 - 58 000; Temps partiel

Résumé du poste

IQVIA is seeking a Clinical Research Coordinator to join our Novi, MI team on-site. This 24-hour/week role involves hands-on procedures, subject recruitment, data collection, and ensuring study conduct adheres to GCP and protocol requirements.

Under supervision of a principal investigator, you will perform ECGs, vital signs, and sample collection, maintain study documents, and support logistics for ongoing trials. Bachelor’s degree preferred with 1+ year of clinical research experience.

Qualifications

• Bachelor’s degree or equivalent in a relevant field.
• Minimum 1+ year of clinical research experience.
• Familiarity with GCP, medical terminology, and patient safety.

Responsabilités

• Perform ECGs, sample collection, and vital signs.
• Coordinate studies and ensure GCP compliance.
• Prepare materials, set up equipment, plan logistics.
• Recruit, screen, and orient patients.
• Record data in CRFs with accuracy.
• Collaborate with investigators and monitors.

Connaissances

Prescreening experience

EDC systems proficiency

Clinical data management

Attention to detail

Formation

Bachelor’s degree or equivalent

Outils

EDC systems

Description du poste

Clinical Research Coordinator - Novi, MI### Clinical Research Coordinator - Novi, MIApply: Novi, MI: Part time: Posted Today: R1577430# **Clinical Research Coordinator - Novi, MI****Work Set-Up:** On-site **Schedule Weekly Hours:** 24 hours/week About IQVIAIQVIA 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 RoleWe 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 ECG, sample collection, and vital signs.* Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.* Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.* Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.* Collect and accurately record clinical data in case report forms (CRFs).* Collaborate with investigators and monitors, addressing queries and ensuring data quality.* 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 with prescreening patients based on inclusionary/exclusionary criteria.*** **Familiarity with patient chart/medical record review.*** **Ability to support patient study visits.*** Strong attention to detail and ability to establish effective working relationships.* Proficiency with **EDC systems**, data entry accuracy, and query management.**Please note:** *This position is not eligible for sponsorship.* #LI-CES #LI-DNP #LI-HCPIQVIA 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.comIQVIA 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. https://jobs.iqvia.com/eoeIQVIA 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.