Research Associate III (JR233829)

Montefiore Hudson Valley Collaborative; New York (NY); On-site; USD 85,000 - 115,000; Full time

Job summary

Montefiore is seeking a Cancer Clinical Trials Senior Research Associate to support the research team with Good Clinical Practice in the conduct of clinical trials. The role leads a disease group, mentors junior staff, and ensures timely collection and shipment of study data and samples as required.

The candidate will typically hold a life sciences or public health degree with clinical research experience and must maintain high standards of accuracy while coordinating multiple tasks and

Qualifications

• Bachelor's degree in life sciences or public health required; Master’s degree preferred.
• ACRP or SOCRA certification required 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.
• Demonstrated leadership potential.

Responsibilities

• Obtain informed consent for non-interventional studies and manage data collection, maintenance, and submission per Sponsor guidelines.
• Attend clinics as needed to support recruitment activities and administer questionnaires.
• Contribute to development of research protocols and understanding of study design; assist with data audits.

Education

Bachelor's degree in life science or public health

Masters 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. The Senior Research Associate ensures timely collection of protocol data and samples including shipment to outside entities as required.

Responsibilities

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 Degree required - Bachelor's degree in life science or public health, preferred
• Masters 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