Senior Research Associate, Cancer Clinical Trials Lead

3000 Montefiore Medical Center; United States; On-site; USD 68,000 - 85,000; Full time

Job summary

Montefiore Medical Center in Bronx, NY seeks a Senior Research Associate for the Cancer Clinical Trials Office. The role leads the disease group, mentors junior staff, and ensures accurate data collection and protocol compliance.

Responsibilities include obtaining informed consent for non-interventional studies, coordinating data submission, and assisting with recruitment and study design. Strong communication and organizational skills required.

Qualifications

• Bachelor's degree in life science or public health required/preferred Master’s degree preferred Medical Degree (or foreign equivalent) required or preferred
• ACRP (or SOCRA) certification required within 18 months of employment
• 3 years of work experience required; GCP training required
• MS Office proficient; Life Sciences or Public Health background preferred
• Excellent written and oral communication skills; attention to detail; leadership potential

Responsibilities

• Lead Research Associate for the disease group with mentoring, training and data review of junior staff
• Ensure timely collection of protocol data and samples and shipment as required
• Obtain informed consent for non-interventional studies and maintain study information
• Assist recruitment activities and administer questionnaires as needed
• Contribute to development of research protocols and DB enhancements

Skills

Leadership

Communication skills

Attention to detail

Multitasking

Education

Bachelor's degree in life science or public health

Master's degree preferred

Medical Degree (or foreign equivalent)

ACRP or SOCRA certification within 18 months

3 years of work experience

GCP training

MS Office proficient

Life Sciences or Public Health background

Tools

MS Office

Job description

Montefiore Medical Center in Bronx, NY seeks a Senior Research Associate for the Cancer Clinical Trials Office. The role leads the disease group, mentors junior staff, and ensures accurate data collection and protocol compliance.

Responsibilities include obtaining informed consent for non-interventional studies, coordinating data submission, and assisting with recruitment and study design. Strong communication and organizational skills required.