Research Coordinator (Clinical Research)
Мэтч & Сопровод
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Описание вакансии
TL;DR
Research Coordinator (Clinical Research): Managing the day-to-day execution of clinical research studies at an investigative site with an accent on regulatory compliance and data integrity. Focus on coordinating patient enrollment, maintaining source documentation, and ensuring adherence to ICH-GCP and FDA guidelines.
Location: Hybrid on-site in McComb, Mississippi, USA
Company
is an independent technology consulting firm providing guidance and solutions across Information Systems, Telecom, Life Sciences, and Engineering.
What you will do
- Coordinate patient enrollment activities and ensure participant safety and confidentiality.
- Collect, review, and maintain source documentation and regulatory binders.
- Enter study data into Electronic Data Capture (EDC) systems and resolve data queries.
- Prepare for and support sponsor monitoring visits, audits, and site inspections.
- Collaborate with investigators, radiology staff, and study teams to ensure protocol compliance.
Requirements
- Bachelor's degree in a related field.
- 5 years of Clinical Research Coordination experience.
- Strong understanding of ICH-GCP guidelines, FDA regulations, and IRB submissions.
- Experience with Electronic Data Capture (EDC) systems, specifically Medidata Rave.
- Ability and willingness to travel on-site to McComb, Mississippi.
Nice to have
- Experience in an imaging environment, particularly with CT, to support imaging-related study activities.
Culture & Benefits
- International community comprising more than 110 different nationalities.
- Strong internal growth trajectory, with 70% of leaders starting at entry level.
- Access to a robust training system via an internal Academy with 250+ modules.
- Dynamic work environment featuring regular internal events and team buildings.
Hiring process
- Brief virtual or phone introductory call to discuss motivations and fit.
- Average of 3 interviews with the line manager and team members.
- Optional case study or technical assessment depending on the role's requirements.
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