Research Coordinator

Weill-Cornell-Medicine-aed1176; New York (NY); On-site; USD 90,000 - 110,000; Full time

Job summary

Weill Cornell Medicine in New York is seeking a data-focused professional to oversee clinical trial data management, regulatory and financial aspects of studies under direction.

You will coordinate budgets, support protocol development, ensure regulatory compliance with SOPs, FDA and NIH guidelines, and collaborate with sponsors and sites to streamline recruitment and data reporting.

Qualifications

• Bachelor's degree in a related field.
• Approximately 2 years of health-related or clinical research experience.
• Familiarity with IRB processes and regulatory policies.

Responsibilities

• Monitors data management and regulatory aspects of clinical trial operations.
• Coordinates data collection from multiple sites and assists in budget preparation.
• Ensures compliance with SOPs, FDA, NIH regulations for reporting events to regulatory agencies.
• Develops regulatory reports and associated documentation.
• Supports protocol development related to patient recruitment and retention.
• Performs monitoring visits and collaborates with sponsor/site personnel on regulatory issues.

Skills

Clinical data management

Regulatory compliance

IRB familiarity

Budget coordination

Education

Bachelor's Degree in related field

Tools

CDMS

Job description

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

Position Summary

Under direction, monitors all data management, regulatory and financial aspects of clinical trial operations. This role also coordinates special research projects, prepares internal board protocols for clinical research, assists in the design of evaluation tools/instruments and coordinates budgets.

Job Responsibilities

• Develops and implements practices to ensure research efficiency by routinely analyzing and evaluating workflow.
• Coordinates the collection, compilation, documentation and analysis of clinical research data from various clinical sites. Assists in the determination of guidelines for the collection of clinical data and or administration of clinical studies.
• Ensures compliance of general and study specific regulatory related processes with SOPs, FDA, NIH, and applicable regulations for the reporting of events to regulatory agencies.
• Develops regulatory reports and associated documentation in accordance with SOPs and study specific processes.
• Prepares study related budgets for granting agencies. Negotiates study related budgets with various sites, departments and sponsors.
• Researches and develops the recruitment strategies. Employs modeling and simulation tools to understand the current and projected outcome of recruitment techniques. Monitors and evaluates the success of varying subject recruitment techniques.
• Participates in protocol development as it relates to patient recruitment. Assesses, analyzes, prepares and submits departmental protocols to various places as it relates to subject recruitment and retention.
• Performs monitoring visits: pre-study, initiation, routine monitoring and closeout visits.
• Works closely with sponsor, site and study personnel on relevant regulatory issues. Develops policies and procedures pertaining to regulatory and monitoring processes. Leads regulatory educational training events for personnel at various sites.
• Maintains inventory of supplies, equipment and/or reagents. May order supplies/equipment/reagents as authorized or ensure that needs are escalated appropriately. Receives supply orders and confirms accuracy of delivery. May assist with cost control.
• Performs other related duties as directed.

Education

• Bachelor's Degree in related field

Experience

Approximately 2 years of experience in health-related role, in clinical or research setting

Knowledge, Skills and Abilities

• Experience with conducting and carrying out protocols and research coordination.
• Familiarity with IRB interaction, regulatory policies, database input and report generation.
• Research experience in an academic health center with exposure to a team research environment at all levels (senior investigators, nurses, research coordinators, lab technicians).

Licenses and Certifications

Working Conditions/Physical Demands

Standard office work

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