Research Associate (JR227722)

ViziRecruiter,LLC.; New York (NY); On-site; USD 50,000 - 70,000; Full time

Job summary

A healthcare organization is seeking a Research Associate to work with Principal Investigators in clinical research studies. Responsibilities include overseeing data integrity, managing study information, and preparation of research presentations. Candidates should have relevant education, experience in data management, and strong team collaboration skills. The position is based in New York, NY, and offers the potential for growth within the research field.

Qualifications

• High school diploma/GED required + 10 Years' Experience.
• Associate degree required + 5 Years' Experience.
• Experience creating Redcap database; ability to input and maintain participant data.

Responsibilities

• Supervise study information maintenance.
• Manage data collection, analysis, and cleaning.
• Facilitate preparation of conference materials.

Skills

Data entry

Team collaboration

Research protocol adherence

Bilingual Spanish fluency

Education

High school diploma/GED

Associate degree

Bachelor's degree

Tools

Redcap

Velos

Brany

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

The Research Associate will work directly with Principal Investigators within the OBGYN Research Division on the execution of research studies focusing on protocol development, coordination, and data cleaning and monitoring. The Research Associate manages research project activities ensuring the quality and integrity of data collection, and trains, manages, and supports students, staff and interns. The Research Associate will also review work products to ensure study protocol is followed as written and approved by the institution's IRB. The position has substantial potential for growth with the goal of progressing to involvement at all levels of research design and implementation on multiple clinical research studies.

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

• High school diploma/GED required + 10 Years' Experience.
• Associate degree required + 5 Years' Experience.
• Bachelor's degree preferred.
• 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.