Research Associate III (JR229826)

ViziRecruiter,LLC.; New York (NY); On-site; USD 85,000 - 105,000; Full time

Job summary

Montefiore Cancer Center seeks a Senior Research Associate to lead the disease group in cancer clinical trials, mentor junior staff, and ensure data accuracy under GCP. The role requires independent function and leadership in trial oversight.

The candidate will manage protocol data, obtain informed consent for non-interventional studies, assist with recruitment, and contribute to protocol development and database improvements.

Qualifications

• Bachelor's degree in life science or public health.
• Master's degree preferred.
• Medical degree (or foreign equivalent) preferred.
• ACRP or SOCRA certification within 18 months of employment.
• 3 years of work experience required.
• GCP training required.
• Life Sciences or Public Health background preferred.
• Excellent written and oral communication skills.

Responsibilities

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

Skills

Communication skills

Attention to detail

Leadership potential

Multitasking

Education

Bachelor's degree in life science or public health

Master's degree

Medical Degree (or foreign equivalent)

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.