At Memorial Sloan Kettering (MSK), we're not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward with innovation and discovery, we're driving excellence and improving outcomes. We're treating cancer, one patient at a time. Join us and make a difference every day.
In compliance with applicable State regulatory authorities, COVID-19 vaccination 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 vaccine requirement are permitted for those who request and receive an approved medical or fully remote exemption. Requests for medical exemption can take up to two weeks to review. Vaccination or an approved medical exemption is required to start work.
*Staff working at a MSK New Jersey location must be up to date with COVID-19 vaccination, which includes having completed the primary COVID-19 vaccination series and booster once eligible as mandated by New Jersey State. All New Jersey staff not yet eligible for a booster must receive a booster within 3 weeks of becoming eligible as a condition of continued employment at MSK.
Note: Individuals are eligible to receive a COVID-19 booster two months after completion of a primary vaccination series for COVID-19. Because vaccine-induced immunity can wane over time, MSK continues to strongly urge all staff to get a COVID-19 booster as soon as they become eligible to maintain their protective immunity for a longer period.
The Prostate Cancer Clinical Trials Consortium (PCCTC) is the nation's premier multicenter Clinical Research Organization specializing in ground breaking prostate cancer research. We work together with distinguished investigators on a single mission: to design, implement and complete hypothesis-driven studies in prostate cancer, translating scientific discoveries to improved standards of care. We are currently hiring a Monitoring Manager to join our dynamic clinical research team. Join us today and help make a difference every day!
Ensure appropriate monitoring oversight activities for the PCCTC's clinical research portfolio, ensuring monitoring oversight adheres to all federal regulatory requirements and International Center for Harmonization guidance on Good Clinical Practice.
Lead, mentor, and develop the clinical research monitoring team to ensure that monitoring occurs according to PCCTC SOPs and study-specific monitoring plans.
Review trip reports, expense reports, and invoices related to monitoring activities; contribute to financial planning for the monitoring program.
Lead strategic planning to develop monitoring plans and determine monitoring team allocations in order to meet company and study-specific objectives.
Develop analytical methods to track monitoring results and findings to measure impact and success, including real-time feedback.
Work with PCCTC leadership to develop and implement continuous quality improvement and inspection readiness initiatives.
Able to plan, prioritize, facilitate and lead meetings, to develop programs, to manage research projects and to prioritize work across a portfolio of projects.
An effective communicator, capable of resolving how best to reach different audiences and executing communications based on that understanding.
Adept in setting priorities, meeting established deadlines, leading multiple large scale projects simultaneously and guiding staff to ensure activities adhere to established time frames and deadlines.
7+ years of clinical research experience.
4+ years monitoring experience.
Broad-based and detailed knowledge of Human Subjects Protection, Good Clinical Practice, FDA requirements, clinical research-related federal regulations, HIPAA.
Outstanding communication and presentation skills, both oral and written.
A strong ability and understanding on how to collect, analyze, interpret and prepare data for presentation and solve problems.
This is a full-time remote position with the possibility of occasional travel for monitoring/monitoring oversight visits or in-person meetings.
Pay Range $104,600.00-$167,400.00
Please click to learn more about MSK's compensation philosophy.
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.
At Memorial Sloan Kettering (MSK), we’re not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward with innovation and discovery, we’re driving excellence and improving outcomes. For the 28th year, MSK has been named a top hospital for cancer by U.S. News & World Report. We are proud to be on Becker’s Healthcare list as one of the 150 Great Places to Work in Healthcare in 2018, as well as one of Glassdoor’s Employees’ Choice Best Place to Work for 2018. We’re treating cancer, one patient at a time. Join us and make a difference every day.