Research Associate III (JR229247)

ViziRecruiter,LLC.; New York (NY); On-site; USD 90,000 - 130,000; Full time

Job summary

Montefiore is seeking a Cancer Clinical Trials Senior Research Associate to support the research team in conducting clinical trials in accordance with Good Clinical Practice. The role includes independent work, mentoring junior researchers, and reviewing data accuracy within the disease group.

The position requires a Bachelor’s in life sciences or public health (Master’s preferred), GCP training, and 3 years of experience, with ACRP/SOCRA certification to be earned within 18 months of hire.

Qualifications

• Bachelor's degree in life science or public health is required, master’s preferred.
• ACRP or SOCRA certification due within 18 months of employment.
• 3 years of work experience in related field.
• GCP training is required.

Responsibilities

• Ensure timely collection of protocol data and samples, including shipment as required.
• Obtain informed consent for non-interventional studies and manage data submission per Sponsor.
• Attend clinic to assist recruitment activities and administer questionnaires.
• Contribute to development of research protocols and database enhancements.

Skills

Communication skills

Attention to detail

Multi-tasking

Leadership potential

Clinical research concepts

Education

Bachelor's degree in life science or public health

Master's degree

Medical degree or foreign equivalent

ACRP or SOCRA certification

Tools

MS Office

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 Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice. The Senior Research Associate is able to function independently and is the lead Research Associate for the disease group which includes mentoring, training and reviewing/auditing accuracy of data of the junior Research Associates.

Responsibilities

• The Senior Research Associate ensures timely collection of protocol data and samples including shipment to outside entities as required.
• This individual obtains informed consent of non-interventional studies, collects, maintains and organizes study information including compilation, registration and submission of data, as required by the Sponsor.
• Attends clinic as needed to perform activities including but not limited to assisting the research team with recruitment activities, administering questionnaires.
• Contributes to the development of research protocols and understanding research design, including assisting with database enhancements.

Requirements

• Bachelor's Degree required - Bachelor's degree in life science or public health, preferred.
• Master's Degree preferred.
• Medical Degree (or foreign equivalent), Preferred.
• ACRP (or SOCRA) certification required within 18 months of employment.
• 3 years of work experience required.
• GCP training required.
• MS Office proficient.
• Life Sciences or Public Health background preferred.
• Excellent written and oral communication skills.
• Exceptional attention to detail and accuracy.
• Ability to manage multiple tasks & priorities.
• Demonstrated leadership potential.
• Knowledge of variety of concepts, practices and procedures in directly related field.