Research Associate (JR230830)

Montefiore Hudson Valley Collaborative; New York (NY); Sur place; USD 55 000 - 75 000; Plein temps

Résumé du poste

ViziRecruiter,LLC. is seeking a Clinical Research Coordinator I to assist in the conduct of clinical trials. This role involves collecting and managing patient clinical data, obtaining informed consent, and ensuring compliance with Good Clinical Practice.

The ideal candidate should have a Bachelor's degree, with a Master's degree preferred, along with relevant certifications. Responsibilities include data collection, subject screening, and coordination of study activities.

Qualifications

• Bachelor's Degree is required for this role.
• Master's Degree is preferred for better competency.
• ACRP (or SOCRA) certification is a plus.
• Medical Degree or equivalent is a valuable asset.

Responsabilités

• Collects and records study data. Inputs all information into database.
• Assists in clinical research activities like screening participants.
• Maintains source documents and subject files per hospital procedures.
• Ensures accurate compilation of subject data through reviews.
• Coordinates scheduling for multiple studies under supervision.
• Secures and ships clinical specimens as required by protocols.

Formation

Bachelor's Degree

Master's Degree

ACRP (or SOCRA) certification

Medical Degree (or foreign equivalent)

Description du poste

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: assisting the research team with recruitment activities, administering 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.
• Medical Degree (or foreign equivalent) Preferred.