Regulatory Specialist

Weill Cornell Medicine; New York (NY); On-site; USD 60,000 - 67,000; Full time

Job summary

Weill Cornell Medicine, located on the Upper East Side, seeks a Regulatory Specialist to oversee clinical trial regulatory maintenance from study submission through closeout.

You will coordinate protocol submissions, enroll subjects per regulations, and manage regulatory documents; non-exempt, 35 hours per week.

Qualifications

• Bachelor's Degree in related field.
• Approximately 2 years of clinical research experience in a healthcare setting.
• Master's degree can substitute for experience.

Responsibilities

• Coordinates all aspects of protocol submissions to CSEC, IRB and committees.
• Facilitates enrollment of research subjects in compliance with regulations.
• Reviews subject eligibility and regulatory compliance for enrollment.
• Performs central subject registration for specified studies.
• Reports Serious Adverse Events to IRB and agencies.
• Prepares regulatory documents for sponsor/CRO.
• Maintains regulatory records and deadlines.
• Provides training on subject registration and regulatory processes.
• Maintains listings of active studies for investigators.
• Serves as a resource on protocols and investigational activities.
• Assists with investigator-initiated trials.
• Coordinates site visits and audits of clinical trials.
• Attends conferences and disseminates information to staff.
• Maintains electronic and hard copy files.

Skills

Communication & interpersonal skills

MS Office

Database applications

Organizational skills

Regulatory knowledge

Attention to detail

Multi-tasking

Professionalism

Education

Bachelor's Degree in related field

Job description

• As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices

Title: Regulatory Specialist

Location: Upper East Side

Org Unit: Neurological Surgery

Work Days

Weekly Hours: 35.00

Exemption Status: Non-Exempt

Salary Range: $43.30 - $48.41

• As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices

Position Summary

Oversees the clinical trial regulatory maintenance from study submission through closeout.

Job Responsibilities

• Coordinates all aspects of protocol submission for research projects. Prepares and submits all necessary documents to the Clinical Science Evaluation Committee (CSEC), the Institutional Review Board (IRB) and ancillary committees.
• Works with the research team to facilitate the enrollment of research subjects in compliance with established regulations and guidelines.
• Reviews and confirms subject eligibility and regulatory compliance for enrollment. Submits eligibility exceptions to the IRB.
• Performs central subject registration for specified research studies.
• Reports all Serious Adverse Events (SAEs) to the Institutional Review Board and other agencies, as required.
• Prepares and submits all regulatory documents to sponsor and/or contract research organization (CRO).
• Ensures maintenance of up-to-date regulatory records and compliance with industry deadlines.
• Provides training to junior and new staff on subject registration and regulatory processes and procedures.
• Maintains and disseminates accurate listings of active and potential studies to participating investigators.
• Serves as the resource for detailed information on assigned protocols and other investigational research activities.
• Provides assistance for specified investigator-initiated trials.
• Coordinates site visits and audits of clinical trials.
• Attends conferences regarding clinical trials and disseminates information to clinical staff.
• Maintains electronic and hard copy files.

Education

• Bachelor's Degree in related field

Experience

Approximately 2 years of prior clinical research experience in a healthcare setting.

Master's degree in a related field can be substituted for experience.

Demonstrated knowledge and understanding of clinical research.

Knowledge, Skills and Abilities

• Demonstrated strong communication and interpersonal skills; demonstrated ability to interact with multiple constituencies and exercise "people skills".
• Demonstrated proficiency with MS Office Suite and database applications.
• Demonstrated organizational skills and ability to pay close attention to detail.
• Demonstrated critical thinking and analytical skills.
• Demonstrated ability to multi-task and prioritize in a fast-paced environment.
• Demonstrated ability to remain focused despite frequent interruptions.
• Ability to treat confidential information with utmost discretion.
• Demonstrates ability to exercise standards of professionalism, including appearance, presentation and demeanor.
• Demonstrated ability to work effectively in a collaborative manner with all departmental faculty and staff, as well as other institutional representatives.

Working Conditions/Physical Demands

Standard office work

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