Research Associate III (JR228907)

ViziRecruiter,LLC.; New York (NY); On-site; USD 70,000 - 90,000; Full time

Job summary

A healthcare organization based in New York seeks a Senior Research Associate to lead clinical trial activities. The role involves mentoring junior associates, ensuring timely data collection, and contributing to research protocol development. Ideal candidates will possess a Bachelor's degree in life science or public health, with additional degrees preferred. Strong communication skills and attention to detail are essential for success in this position.

Qualifications

• Bachelor's degree required, preferably in life science or public health.
• Master's Degree or Medical Degree preferred.
• ACRP (or SOCRA) certification required within 18 months of employment.
• 3 years of work experience required with GCP training.

Responsibilities

• Ensure timely collection of protocol data and samples.
• Obtain informed consent of non-interventional studies.
• Assist research team with recruitment activities.
• Contribute to the development of research protocols.

Skills

Excellent written and oral communication skills

Exceptional attention to detail

Ability to manage multiple tasks & priorities

Demonstrated leadership potential

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 assists 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.