Research Coordinator
$56,347–$76,003 year
On-siteFreehold, New Jersey, United States
Job Summary
Oversee assigned clinical trials from start to finish by demonstrating protocol understanding, screening and enrolling patients via EMR and EDC, and scheduling follow-up visits for clinicians, nurses, and imaging. Maintain enrollment logs, enter data within 24 hours of collection, and resolve queries in five days. Manage study drug accountability, process biological materials, and ensure compliance with RCCA SOPs, HIPAA, and FDA guidelines. Monitor patient safety, adverse events, and protocol deviations, reporting occurrences to the PI and Clinical Trial Management. Collaborate with cross-functional teams, sponsors, and IRBs to address regulatory issues and support internal and external audits. Conduct weekly and monthly trial meetings while tracking patient reimbursements.
Required Qualifications
- Minimum 1 year of experience with oncology interventional clinical trials
- ACRP (CCRC, CCRA) or SoCRA (CCRP) Certified Clinical Research Professional with one year of oncology trial experience
- High School diploma with four years of oncology clinical trial experience
- Computer literate
- Good interpersonal skills
- Good writing skills
- Good verbal communication skills
- Must be available to work and travel onsite Monday to Friday from 9 am to 5 pm in all RCCA network
- Ability to multi-task
- Ability to prioritize
- Ability to work in a fast-paced work environment
- Time management skills
- Ability to work well under pressure
Desired Qualifications
- Previous regulatory affairs experience
- Prior experience working with centrifuge
- Prior experience handling biofluid specimens
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