Research Associate III (JR226738)

ViziRecruiter,LLC.; New York (NY); On-site; USD 85,000 - 120,000; Full time

Job summary

A leading healthcare organization in New York is seeking a Senior Research Associate to support clinical trials. This role involves independent functioning, mentoring junior associates, and ensuring accurate data collection. Qualifications include a Bachelor's degree in life sciences or public health, 3 years of relevant experience, and proficiency in MS Office. The organization offers opportunities for growth and promotes an inclusive work environment.

Qualifications

• Bachelor’s degree required; preferred in life science or public health.
• 3 years of work experience required.
• GCP training required.
• ACRP or SOCRA certification required within 18 months of employment.
• 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.

Responsibilities

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

Skills

MS Office proficiency

Excellent written and oral communication skills

Exceptional attention to detail and accuracy

Demonstrated leadership potential

Ability to manage multiple tasks & priorities

Education

Bachelor’s Degree in life science or public health

Master’s Degree preferred

Medical Degree or foreign equivalent preferred

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 مهمة 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, administer questionnaires.
• Contributes to the development of research protocols and understanding research design including assistance 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.

Montefiore Medical Center is an equal employment opportunity employer. Montefiore Medical Center will recruit, hire, train, transfer, promote, layoff and discharge associates in all job classifications without regard to their race, color, religion, creed, national origin, alienage or citizenship status, age, gender, actual or presumed disability, history of disability, sexual orientation, gender identity, gender expression, genetic predisposition or carrier status, pregnancy, military status, marital status, or partnership status, or any other characteristic protected by law.