Research Associate (JR235177)

Montefiore Hudson Valley Collaborative; New York (NY); Presencial; USD 65.000 - 90.000; Tempo integral

Resumo da vaga

Montefiore Health System seeks a Cancer Clinical Trials CRC I to support the research team under supervision. You will handle primary data collection, manage patient information, and assist with protocol related samples while ensuring compliance with Good Clinical Practice.

You will participate in recruitment activities, obtain informed consent for studies, and help organize data submission, registrations, and source documents across multiple studies at the site in New York.

Qualificações

• Bachelor's degree required.
• Masters degree preferred.
• ACRP or SOCRA certification preferred.
• Life science/public health degree preferred.
• Medical degree preferred.

Responsabilidades

• Collects and records study data; inputs into database.
• Assists in recruitment activities and screening.
• Maintains source documents and subject files per procedures.
• Coordinates SFV, SIVs and monitor scheduling, including remote access.

Conhecimentos

Data collection

Data entry

Study coordination

Informed consent

Source documents

Formação

Bachelor's degree

Master's degree

ACRP certification

SOCRA certification

Life science/public health degree

Medical degree

Descrição da vaga

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 CRC I under direct supervision supports the research team in overall conduct of clinical trials using Good Clinical Practice. Mentored by an experienced Clinical Research Coordinator II or Sr. Clinical Research Coordinator, the CRC I is responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials.

Ensures timely collection of protocol related samples including shipment to outside entities as required. This individual obtains informed consent for non-interventional studies, participates and supports investigators in the informed consent process for interventional trials, 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: assist the research team with recruitment activities, administer questionnaires.

Responsibilities

• Collects and records study data. Inputs all information into database
• Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
• Maintains source documents and subject files in accordance with hospital procedures.
• Ensures accurate and complete compilation of subject data through chart reviews.
• Upon assignment and under direct supervision, coordinates SFV, SIVs and monitor scheduling-- including remote access setup--for multiple studies.
• Secures, delivers and ships clinical specimens as required by the protocol.

Requirements

• Bachelors Degree Required
• Masters Degree Preferred
• ACRP (or SOCRA) certification preferred
• Bachelor's degree in life science or public health, preferred
• Medical Degree (or foreign equivalent), Preferred