Job Description

The  Research Associate I will oversee multiple clinical trials, serving as a point person for patients, their family members, and the clinical study team. The position consists of working with various departments across the hospital, including forging new partnerships with departments to ensure completion of trial-related activities. The clinical research coordinator I will direct participants and study team members to adhere to the study protocol and rules and regulations governed by regulatory bodies including Institutional Review Boards and the FDA.

Job Responsibilities

- Directing seamless flow of daily trial-related activities, including data entry, consent and recruitment and clinical assessments as required by the study protocol of the study subjects.

- Directing strict adherence to the study protocols, as well as sponsor, FDA and other regulatory authority requirements.

- Developing workflows for clinical trial, including reminders/updates to the clinical team.

- Coordinating team members to complete both clinical and non-clinical assessments per protocol. This includes developing workflow for patient care such as assigning secretaries to schedule patients, developing workflow with ancillary departments (such as radiology, advanced imaging, pathology, pharmacy), and assigning appropriate clinical team members such as doctors to complete clinical tasks such as reviewing adverse events versus assigning non-clinical team members to complete non-clinical tasks such as administering questionnaires to a patient.

-Prepares and submits all protocol applications, amendments, continuing reviews, and informed consent documents for IRB review and approval.

- Executing patient billing in multiple databases including the patient’s electronic medical record.

- Developing action plans for ensuring all study tasks are completed as required per the protocol and developing subsequent corrective action plans if any errors are made.

-Coordinates assigned study monitoring and auditing visits with study coordinator, investigator, industry sponsors, and internal/external auditors.

The Research Associate I will be trained to be highly specialized in clinical trials assigned to them and is expected to be able to manage clinical trial projects independently after sufficient training is completed

QUALIFICATIONS:

• Bachelors Degree required
• GCP training required
• A record of clinical research
• Publication from prior research work
• MS Office proficient. 
• 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 

Department: Cardiology Bargaining Unit:  Non Union Campus:  MOSES Employment Status:  Regular Full-Time Address: 3319 Rochambeau Avenue, Bronx
Shift:  Day Scheduled Hours: 8:30 AM-5 PM Req ID: 225297 Salary Range/Pay Rate: $62,400.00- $64,350.00   

For positions that have only a rate listed, the displayed rate is the hiring rate but could be subject to change based on shift differential, experience, education or other relevant factors.

To learn more about the “Montefiore Difference” – who we are at Montefiore and all that we have to offer our associates, please click 

Montefiore is an equal employment opportunity employer. Montefiore 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. 

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