RESEARCH ASSOCIATE - PER DIEM (JR227940)

ViziRecruiter,LLC.; New York (NY); On-site; USD 65,000 - 95,000; Full time

Job summary

A leading healthcare organization in New York is looking for a candidate to supervise study information and manage data collection for clinical research. This role requires a Bachelor's degree, or an Associate degree with 5 years of experience, or a high school diploma with 10 years of experience. Candidates should have experience with Redcap and be bilingual in Spanish. Strong commitment to clinical research and teamwork is essential. Competitive compensation and benefits are offered for this position.

Qualifications

• Bachelor's degree preferred.
• Associate degree required + 5 Years' Experience.
• High school diploma/GED required + 10 Years' Experience.
• Experience creating Redcap database; ability to input and maintain participant data.
• Bilingual Spanish oral and written fluency preferred.
• Strong interest and commitment to clinical research.
• Ability to work well in a team and independently.

Responsibilities

• Supervise maintenance of study information such as enrollment and participants interviewed.
• Data entry in Velos, Brany, Sponsor's EDC.
• Manage data collection, analysis, and cleaning.
• Develop progress reports for the PI and study funding agency.
• Facilitate preparation of conference abstracts and publications.
• Perform other administrative duties as needed.

Skills

Data entry

Team collaboration

Database management

Bilingual Spanish fluency

Clinical research interest

Education

Bachelor's degree

Associate degree + 5 years' experience

High school diploma/GED + 10 years' experience

Tools

Redcap

Velos

Brany

Sponsor's EDC

Job description

Introduction

To heal, to teach, to discover and to advance the health of the communities we serve.

To learn more about the “Montefiore Difference” – who we are at Montefiore and all that we have to offer our associates, please click here.

Overview

For positions that have only a rate listed, the displayed rate is the hiring rate but could be subject to change based on shift differential, experience, education or other relevant factors.

Responsibilities

• Supervise the maintenance of study information such as enrollment, participants interviewed.
• Data entry in Velos, Brany, Sponsor's EDC and query resolution.
• Manage data collection, analysis and cleaning performing regular audits to ensure that the data collected are complete and accurate, and that the research is being conducted as outlined in the protocol.
• Develop appropriate progress reports for the Pl, study funding agency and the IRB.
• Facilitate the preparation of conference abstracts, oral presentations, poster presentations, and manuscripts for publication in conjunction with PI.
• Perform other administrative duties as needed.

Requirements

• Bachelor's degree preferred.
• Associate degree required + 5 Years' Experience.
• High school diploma/GED required + 10 Years' Experience.
• Experience creating Redcap database; ability to input and maintain participant data.
• Bilingual Spanish oral and written fluency preferred.
• Strong interest and commitment to Clinical Research.
• Ability to work well in a team setting and independently is essential.