13 дней назад
Clinical Research Coordinator (Cardiovascular Studies)
35 - 42$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Clinical Research Coordinator (Cardiovascular Studies) (Clinical Trials/GCP): Supporting cardiovascular clinical trials through patient procedures, study coordination, participant recruitment, and clinical data management with an accent on protocol compliance, participant safety, and data integrity. Focus on conducting ECGs and sample collection, maintaining regulatory documentation, and resolving queries in EDC systems.
Location: On-site in Linden, New Jersey, United States; the position title references Somerset, NJ.
Salary: $35.00–$42.00 per hour.
Company
provides clinical research services, healthcare intelligence, advanced analytics, and technology solutions for pharmaceutical, biotechnology, and medical device companies.
What you will do
- Perform ECGs, vital signs measurements, biological sample collection, and other clinical procedures.
- Coordinate daily clinical research activities according to study protocols and Good Clinical Practice guidelines.
- Recruit, screen, consent, educate, and orient study participants while supporting a safe patient experience.
- Prepare and maintain study materials, equipment, regulatory documentation, and study supplies.
- Collect, document, and enter clinical data into case report forms and electronic data capture systems.
- Collaborate with investigators, monitors, and study teams to resolve queries and maintain data quality.
Requirements
- Bachelor’s degree preferred, or an equivalent combination of education and relevant experience.
- At least 1 year of experience in clinical research or a related healthcare setting.
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Experience conducting study visits, including patient education and chart review.
- Proficiency with electronic data capture systems, accurate data entry, and query resolution.
- This position is not eligible for visa sponsorship.
Nice to have
- Exposure to cardiovascular studies and related clinical procedures.
- Experience maintaining regulatory binders, managing study supplies, and updating study portals.
- Strong attention to detail and the ability to build effective working relationships.
Culture & Benefits
- On-site clinical research environment.
- Collaboration with investigators, monitors, and study team members.
- Health and welfare benefits may be available depending on the position and schedule.
- Additional incentive plans, bonuses, or other compensation may be offered depending on the position.
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