Clinical Research Associate

IRI believes in commitment, Integrity and strategic workforce solutions.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

We’ve stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.

Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients’ success.

Candidate with Academic CRO experience would also be fine, leading the study(3-4 studies)
Understands data management and documentation process
Candidate who has worked on clinical trials as clinical data manager, CRF design and clinical data management plan, study maintenance
Works with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and other Clinical, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting.
Demonstrates a general understanding of each assigned protocol, critical tasks and milestones.
Ensure completeness, correctness and consistency of routine clinical data and data structure.
Assists in the implementation of routine clinical data management process with vendors including data entry, data quality checking, data transfer, reporting, backup, and recovery. Assists in the preparation of CRF/eCRF for data collection through the regulatory approval process.
Assists in implementing routine clinical research projects.
Reviews study protocol and assists site coordinators, investigators, and field clinical staff in collecting routine data to meet the protocol requirements in a timely manner.
Identifies, tracks, and resolves routine queries.
Utilizes routine reports to track study progress and ensures timeliness and quality expectations are met.
The ability to problem solve and have people/project leadership skills.Knowledge of FDA regulations, support of needs for NDA and other regulatory submissions, and familiarity with web-based Electronic Data Capture (EDC) and clinical data management systems.

Regards,

Indu Dubey
Clinical Recruiter
732-844-8725 

indu @irionline.com