Clinical Research Manager – Genitourinary Service (GU) Service, Department of Medicine

Job Posting Number: 15978

Research – Clinical
New York, NY
September 13, 2017
Company Overview:

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 27th 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 2016, as well as Glassdoor’s annual Employees’ Choice Awards 2017. We’re treating cancer, one patient at a time. Join us and make a difference every day.

Job Details:

The Genitourinary Service (GU) Service in the Department of Medicine (DoM) at MSK is seeking a Clinical Research Manager (CRM). The CRM serves as an integral member of the research team and oversees the daily operations and activities of the GU research program.

Job responsibilities include but are not limited to:

  • Staff Management: Supervise the training/development and performance management for direct and indirect reports throughout the service.
  • Protocol Development: Oversee all aspects of the protocol development process including protocol, consent and other essential study document drafting. Must be able to write protocols.
  • Financial Management: Works closely with the appropriate stakeholders, forecast trial resource needs, and assesses staffing resource needs for program and senior leadership to ensure appropriate line function allocations.
  • Clinical Trial Reporting: Generate protocol portfolio status reports for key stakeholders. Implements solutions for streamlining and accelerating the monitoring and review of clinical trials to significantly increase accrual to clinical trials, data cleaning, data quality, and trial completion.
  • Quality Assurance: participate in routine audits for data quality, regulatory compliance, patient safety issues related to clinical trial. Communicates and ensures compliance with company policies and procedures, quality standards and improvement initiatives

You need:

  • At Least 4 years of clinical research experience.
  • At least 2 years of direct staff management.
  • Thorough knowledge of Good Clinical Practice (GCP) guidelines, Human Subject Protection, clinical trial design, regulatory processes, and clinical development process required.
  • Therapeutic and Oncology Research experience strongly preferred.
  • Effective written/verbal communication and oral presentation skills required. Excellent interpersonal, leadership, decision-making and issue resolution skills are also required.


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.

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