Research Associate III

Montefiore Mount Vernon; New York (NY); Presencial; USD 68 000 - 85 000; Tempo integral

Resumo da oferta

Montefiore Mount Vernon is seeking a Cancer Clinical Trials Senior Research Associate to support clinical trials under Good Clinical Practice. The role leads the research team within the disease group, mentoring junior staff, auditing data accuracy, and ensuring timely data collection and sample handling as required by the Sponsor.

The incumbent will obtain informed consent for non-interventional studies, compile and submit data, attend clinics for recruitment activities, and contribute to

Qualificações

• Bachelor Degree in life science or public health, preferred.
• Masters Degree preferred.
• Medical Degree (or foreign equivalent), Preferred.
• ACRP (or SOCRA) certification required within 18 months of employment.
• 3 years of work experience required.
• GCP training required.

Responsabilidades

• Lead Research Associate for the disease group, mentoring and training.
• Ensure timely collection and accuracy of protocol data and samples.
• Obtain informed consent for non-interventional studies and manage data submission.
• Assist with recruitment activities and administering questionnaires; contribute to protocol development.

Conhecimentos

Excellent written and oral comms

Attention to detail

Multi-tasking

Leadership potential

GCP training

Formação académica

Bachelor Degree in life science or public health

Masters Degree preferred

Medical Degree (or foreign equivalent) preferred

ACRP or SOCRA certification within 18 months

Ferramentas

MS Office proficiency

Descrição da oferta de emprego

City/State:

Bronx, New York

Grant Funded:

Yes

Department:

Cancer Clinical Trials Office

Work Shift:

Day

Work Days:

MON-FRI

Scheduled Hours:

9 AM-5:30 PM

Scheduled Daily Hours:

7.5 HOURS

Pay Range:

$68,000.00-$85,000.00

Job Summary

The Cancer Clinical Trials Senior Research Associate supports the research team in the overall conduct of clinical trials using Good Clinical Practice. The Senior Research Associate is able to function independently and is the lead Research Associate for the disease group which includes mentoring, training and reviewing/auditing accuracy of data of the junior Research Associates. The Senior Research Associate ensures timely collection of protocol data and samples including shipment to outside entities as required. This individual obtains informed consent of non-interventional studies, collects, maintains and organizes study information including compilation, registration and submission of data, as required by the Sponsor. Attends clinic as needed to perform activities including but not limited to assisting the research team with recruitment activities, administering questionnaires.Contributes to the development of research protocols and understanding research design including assists with database enhancements.

EDUCATION, TRAINING, LICENSES, REGISTRATIONS, PROFESSIONAL CERTIFICATIONS, AND WORK EXPERIENCE

Bachelor Degree required - Bachelor’s degree in life science or public health, preferred

Masters Degree preferred

Medical Degree (or foreign equivalent), 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

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

Montefiore Medical Center is an equal employment opportunity employer. Montefiore Medical Center 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.