RESEARCH ASSOCIATE I

Montefiore Health System; New York (NY); On-site; USD 62,000 - 65,000; Full time

Job summary

Montefiore Health System seeks a Research Associate I to oversee clinical trials. This role involves managing trial activities, ensuring adherence to regulations, and collaborating with various departments. Candidates should have a Bachelor's degree and experience in clinical research, along with strong communication and organizational skills.

Qualifications

• Bachelor's Degree required.
• GCP training required.
• Experience in clinical research.

Responsibilities

• Direct daily trial-related activities including data entry and recruitment.
• Ensure adherence to study protocols and regulatory requirements.
• Develop workflows and coordinate study monitoring.

Skills

Communication

Attention to detail

Leadership potential

Education

Bachelor's Degree

Job description

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 involves working with various departments across the hospital, including forging new partnerships 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 regulations governed by bodies such as IRBs and the FDA.

Job Responsibilities

1. Directing seamless flow of daily trial-related activities, including data entry, consent, recruitment, and clinical assessments as required by the study protocol.
2. Ensuring strict adherence to study protocols, sponsor requirements, FDA, and other regulatory authorities.
3. Developing workflows for clinical trials, including reminders and updates to the clinical team.
4. Coordinating team members to complete clinical and non-clinical assessments per protocol, including workflow development with ancillary departments and assigning appropriate clinical team members.
5. Preparing and submitting protocol applications, amendments, reviews, and consent documents for IRB approval.
6. Executing patient billing in multiple databases, including the electronic medical record.
7. Developing action plans to ensure completion of study tasks and corrective plans if errors occur.
8. Coordinating study monitoring and auditing visits with relevant stakeholders.

The Research Associate I will be trained to manage clinical trial projects independently after completing sufficient training.

Qualifications:

• Bachelor's Degree required
• GCP training required
• Experience in clinical research
• Publication record from prior research
• Excellent communication skills
• Attention to detail and accuracy
• Ability to manage multiple tasks
• Leadership potential
• Knowledge of relevant concepts, practices, and procedures

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

Note: The listed rate is the hiring rate and may change based on shift differential, experience, education, or other factors.

Learn more about the Montefiore Difference here.

Montefiore is an equal employment opportunity employer. We recruit, hire, train, transfer, promote, layoff, and discharge associates without regard to race, color, religion, creed, national origin, alienage or citizenship, age, gender, disability, sexual orientation, gender identity, genetic information, pregnancy, military status, marital or partnership status, or any other characteristic protected by law.

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Mission: To heal, teach, discover, and advance community health.

Vision: To be a premier academic medical center that transforms health and enriches lives.

Values: Our values define our philosophy of care and inspire us to pursue excellence, including integrity, compassion, collaboration, and innovation.