Research Associate I

Montefiore Hudson Valley Collaborative; New York (NY); On-site; USD 53,040 - 66,300; Full time

Job summary

Montefiore Hudson Valley Collaborative seeks a Research Associate I to manage multiple clinical trials as a patient-facing liaison and trial team lead. You will work with departments hospital-wide to ensure timely completion of trial-related activities, maintaining protocol integrity and regulatory compliance.

The role requires a Bachelor’s degree, GCP training, and proven clinical research experience, with strong communication, attention to detail and the ability to manage multiple priorities.

Qualifications

• Bachelor's degree required.
• GCP training completed.
• Experience in clinical research and trials.
• Strong communication and attention to detail.
• Ability to manage multiple tasks with accuracy.
• Demonstrated leadership potential.

Responsibilities

• Oversee daily flow of trial activities including data entry, consent, recruitment and assessments.
• Ensure adherence to study protocols and regulatory requirements.
• Develop workflows for clinical trial activities and coordinate with radiology, pathology, pharmacy and physicians.
• Prepare protocol documents, amendments and consent forms for IRB review.
• Handle patient billing in multiple databases and maintain protocol compliance.
• Coordinate monitoring, audits and communications with sponsors and auditors.

Skills

Clinical trial coordination

Communication skills

Attention to detail

Leadership potential

Multitasking

MS Office

Education

Bachelor's degree

GCP training

Tools

MS Office Suite

Job description

## Research Associate IApplylocations: 3319 Rochambeau Avenuetime type: Full timeposted on: Posted Todayjob requisition id: JR231784**City/State:**Bronx, New York**Grant Funded:**Yes**Department:**Card-research Administration**Work Shift:**Day**Work Days:**MON-FRI**Scheduled Hours:**8:30 AM-5 PM**Scheduled Daily Hours:**7.5 HOURS**Pay Range:**$53,040.00-$66,300.00The **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