Clinical Trials Research Associate I

Montefiore Hudson Valley Collaborative

New York (NY)

On-site

USD 53,040 - 66,300

Full time

14 days+
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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

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.

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Insurance benefits
Voluntary Benefits program