Company Overview
Medix provides workforce solutions to clients and creates opportunity for talent in the Healthcare, Life Sciences, Engineering and Technology fields. Through our core purpose of positively impacting lives, we have earned our reputation as an industry leader by providing unsurpassed customer service and top quality professionals to our clients.
About the job
Summary Of Responsibilities
The research coordinator assistant is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.
Key Responsibilities:
- Coordinate and oversee clinical trials, ensuring adherence to protocols, timelines, and regulatory requirements.
- Recruit, screen, and enroll study participants while maintaining detailed and accurate records.
- Obtain informed consent and ensure participants’ rights and safety are upheld throughout the study.
- Collect, process, and manage study data in compliance with Good Clinical Practice (GCP) guidelines.
- Communicate effectively with investigators, sponsors, and regulatory agencies.
- Prepare and submit study documentation, including IRB submissions and study updates.
- Monitor inventory of study supplies and ensure proper handling of investigational products.
- Conduct regular audits to ensure compliance with study protocols and regulations.
Requirements:
- Bachelor’s/Associate’s degree or equivalent experience
- 1+ years of experience in Clinical Research
- Phlebotomy experience required
- Healthcare background preferred
Details:
Location: Chester, PA
Pay: $55k-$62k annually (Dependent on background and years of experience)
Hours: Monday – Friday; Normal Business Hours; Onsite 5 Days a Week
Duration: Direct Hire
How to Apply:
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