Research Associate III

City/State:

Bronx, New York

Grant Funded:

Yes

Department:

Card - Cardiology Research

Work Shift:

Day

Work Days:

MON-FRI

Scheduled Hours:

8:30 AM-5 PM

Scheduled Daily Hours:

7.5 HOURS

Pay Range:

$60,000.00-$75,000.00

The Cardiology Clinical Trials Research Associate III supports research team in the overall conduct of clinical trials in accordance with Good Clinical Practices. This role involves collaborating with Cardiology Faculty Physician Investigators and other team members to ensure the effective execution and management of clinical trials at Montefiore. The Research Associate will act as the site research lead for a subgroup of Cardiology clinical trials, providing mentorship, training and review/audit of the work done by junior study team members (such as study supervisors and research technicians)

Job Responsibilities

Collaborates with Cardiology Faculty Physician Investigators (PIs) and other team members to ensure effective execution and conduct of clinical trials

Coordination and management of clinical trials including communication with Sponsors, collaboration with interdisciplinary teams within MMC and with external partners to enhance research outcomes.

Participates in the feasibility and complexity assessment process for new protocols.

Upon assignment and under direct supervision, coordinates SFV, SIVs and monitor scheduling- including remote access setup-for multiple studies.

Oversees subject recruitment, data collection and data entry for clinical trials and registries, while ensuring data integrity

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

Secures, delivers, and ships clinical specimens as required by the protocol.

Maintaining accurate research records of essential research documents and source documentation, as required.

Develops and implements innovative research projects in collaboration with senior researchers, and present research findings at national and international conferences.

Mentors, trains, and reviews the work of new and less experienced clinical research staff including study supervisors and research technicians.

Assists Senior Director of Clinical Trials with completion of performance reviews of junior research associates and provides input as needed for development and corrective action activities

Collaborates with disease team members to develop study level SOPs and processes to ensure successful activation and conduct of assigned clinical trials

Participates in Cardiology board research committee meetings and participates in the development of SOPs, work instructions, education/training sessions and quality improvement projects

Assists in developing and implementing innovative research projects in collaboration with senior researchers, and present research findings at national and international conferences.

Assists in writing grant proposals (as necessary)

Performs other related duties

Requirements/ Qualifications

Master's Degree Required

Medical Degree (or foreign equivalent) Preferred
Completed Internal Medicine and Residency training

3 years work experience

A record of clinical research/trial experience
Publication from MD or prior research work

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.