Memorial Sloan-Kettering Cancer Center Project Associate, PCCTC Clinical Operations – Remote in New York, New York

Pay Range$65,400.00-$101,300.00Company OverviewThe 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. One of the world’s most respected comprehensive centers devoted exclusively to cancer, we have been recognized as one of the top two cancer hospitals in the country by U.S. News & World Report for more than 30 years. Vaccination for COVID-19 and Influenza (flu) is mandatory for all MSK staff. Staff are considered fully vaccinated upon completion of a primary vaccination series for COVID-19 (i.e., one dose of a single dose vaccine or a final dose of a multi-dose vaccine series).Exceptions from the COVID-19 and Influenza (flu) vaccine requirements are permitted for those who request and receive an approved medical, religious, or fully remote exemption. Requests for exemption can take up to two weeks to review. Vaccination or an approved exemption is required to start work. Important Note for MSK Employees:YourCareer 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 DescriptionTheProstate Cancer Clinical Trials Consortium (PCCTC)is currently hiring an experiencedProject Associate (PA)to join our dynamic clinical research team. Join us today and help make a difference! PCCTC is the nation’s world-class multicenter Clinical Research Organization specializing in groundbreaking prostate cancer research. We work together with distinguished investigators on a single mission: we design, implement and complete studies in prostate cancer, translating scientific discoveries to improved standards of care.You Are:• Adept at planning and prioritizing work to meet commitments aligned with organizational goals. • An effective communicator, capable of determining how best to reach different audiences and carrying out communications based on that understanding. • Comfortable working in a fast-paced environment. • Adept at building partnerships and working collaboratively with others to meet shared objectives and goals. • Adept at problem-solving to ensure unforeseen issues are handled appropriately and resolved in a timely fashion.• Effective at taking action to ensure projects stay on schedule and deliverables adhere to established timeframes and deadlines. Flexible and willing to experiment with new ways of working as demands shift. • Comfortable leading and presenting during meetings, which may include internal project meetings, partner meetings, site initiation visits (SIVs), data and monitoring and/or safety review meetings, etc. You Will:• Manage complex multi-institutional clinical trials across a diverse research portfolio.This includes industry-sponsored studies as well as investigator-initiated trials (IITs). Reporting to the Project Manager, the Project Associate ensures we provide the best-in-class support to our participating institutions and industry partners. • Assist in running clinical trials including protocol and informed consent drafting, regulatory document drafting, etc. • Communicate effectively and establish good working relationships with a diverse matrix of trial sites, investigators, pharmaceutical & biotechnology partners, and all other partners of the PCCTC (including Executive Leadership, Clinical Operations, Data Management, Data Science, Business Management, Budgets & Contracts, Medical Writing/Editorial, etc.).• Sustain project workflows and timelines, ensuring deadlines and achievements are met. • Maintain and audit comprehensive, GCP/FDA compliant, Trial Master Files (TMFs) for assigned projects. Manage regulatory approvals (ex. IRB), review and filing of documents. • Synthesize clinical, regulatory, and other clinical trial information into concrete plans. • Provide vital documentation in compliance with existing standard operating procedures, regulatory guidelines, etc. • Assist in drafting and maintaining clinical trial conduct documentation (includes Project Management Plans, Safety Management Plans, Monitoring Plans, Meeting Minutes, etc.).You Need:• 2-4 years of clinical research experience• Consistent record in leading clinical research projects with deadlines. • Solid understanding of the Code of Federal Regulations, Good Clinical Practice, and Human Subjects Protection. • Knowledge and understanding of clinical trial regulatory and its relevant documents (including FDA Form 1572, financial disclosure forms, delegation of authority logs, etc.), as well as safety management. • Strong computing skills including proficiency in MS Office products.• Ability to solve problems by using a logical, systematic, sequential approach, and work productively in a remote work environment. • Effective at multi-tasking, setting priorities among several tasks simultaneously and meeting established deadlines. • Experience working with prostate cancer trials and/or multicenter projects, and pharmaceutical or industry-sponsored studies is a plus. • Experience developing project timelines and Gantt Charts using MS Project is a plus. • Experience using Smartsheet is a plus.Are you ready to learn more about ourBenefits? (Pay Range $65,400.00-$101,300.00Pleaseclick ( to find out more about MSK’s compensation philosophy! #LI-RemoteClosingMSK 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. Stay in touch! Register now to join Memorial Sloan Kettering’sTalent Community ( to receive inside information on our organization and new job opportunities.Job LocationsUSA-NY-New YorkPosted Date10 hours ago(2/1/2024 9:23 AM)Requisition ID 2024-74995Category Research – ClinicalPay Range $65,400.00-$101,300.00Apply tot his job