Research Associate (JR229243)

ViziRecruiter,LLC.; New York (NY); On-site; USD 55,000 - 75,000; Full time

Job summary

Montefiore is seeking a Cancer Clinical Trials CRC I to support the research team in the conduct of clinical trials under Good Clinical Practice. This role focuses on primary data collection and management of patient information for interventional and non-interventional studies, guided by a senior coordinator.

Responsibilities include obtaining informed consent, assisting recruitment, recording data in the database, maintaining source documents, and coordinating scheduling and specimen handling

Qualifications

• Bachelor's Degree required for CRC I position.
• Master's Degree preferred to support clinical trials.
• ACRP or SOCRA certification preferred for credentials.
• Bachelor's in life science or public health preferred.
• Medical degree or foreign equivalent preferred.

Responsibilities

• Collects and records study data; inputs into database.
• Assists in activities related to clinical studies, including screening participants and registering subjects.
• Maintains source documents and subject files per hospital procedures.
• Ensures accurate compilation of subject data through chart reviews.
• Coordinates SFV, SIVs and monitor scheduling, including remote access setup for multiple studies.
• Secures, delivers and ships clinical specimens as required by the protocol.

Skills

Data collection

Clinical research knowledge

Good Clinical Practice (GCP)

Informed consent

Study coordination

Education

Bachelor's Degree Required

Master's Degree Preferred

ACRP/SOCRA certification preferred

Bachelor's in life science or public health 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 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

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