Pay Range

Company Overview

The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission: ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. MSK is dedicated to training the next generation of scientists and clinicians, who go on to pursue our mission at MSK and around the globe.

Please review important announcements about vaccination requirements and our upcoming EHR implementation by clicking here.

Important Note for MSK Employees:

Your Career Hub profile is submitted to the hiring team as your internal resume. Please be sure your profile is fully complete with your skills, relevant experience and education (if required). Click here to learn more. Please note, this link is only accessible for MSK employees.

Job Description

Exciting opportunity at MSK: Join our team as a Research Project Associate! We're looking for a dynamic clinical research professional to support our Early Drug Development service, MSK's Phase 1 research team. This role will focus on ensuring quality assurance of all regulatory documents along with helping to keep the service in an audit-ready state.

Role Overview:

• Perform internal regulatory document reviews, quality control and data analysis for research projects, databases, and research protocols within MSKCC.
• Responsible for audit-related project management activities and for integrity associated with clinical research within the disease management team and/or service specific level.
• Participate in special projects and task forces as determined by management.

Key Qualifications:

• 2-4 years of Clinical Research/Project Management experience.
• 1-2 years of regulatory experience, 2+ years preferred.

Core Skills:

• Extensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA).
• Outstanding attention to detail and strong analytical and interpersonal skills.
• Planning and prioritizing work to meet commitments aligned with organizational goals.
• Critical thinking and problem-solving to ensure unforeseen issues are handled appropriately and resolved in a timely fashion.
• Excellent communication skills and the ability to interact across all levels in a confident, professional manner.
• Enthusiasm and dedication to MSK's vision, mission, and values.

Additional Information:

• Location: BAIC, 300 E 66th Street, NYC
• Schedule: Hybrid
• Reporting to the Clinical Research Manager

Pay Range: $66,500 - $103,100.00

Helpful Links:

• MSK Compensation Philosophy
• Review our great benefits offerings

Learn more about Clinical Research at MSK: Research is integral to our mission at MSK and clinical trials help us discover better forms of patient care and treatment. Our outstanding scientists and clinicians work together to drive innovation and tackle some of the greatest challenges of biomedical science!

Closing

MSK is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sexual orientation, national origin, age, religion, creed, disability, veteran status or any other factor which cannot lawfully be used as a basis for an employment decision.

Federal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.