Clinical Research Manager – Hepatopancreatobiliary, Ophthalmic, & Dental Services – Department of Surgery
Job Posting Number: 22357
New York, NY
May 11, 2018
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.
The Hepatopancreatobiliary, Ophthalmic and Dental Services in the Department of Surgery (DoS) at Memorial Sloan Kettering Cancer Center 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 program including management of all therapeutic, non-therapeutic, retrospective, and biospecimen studies, including open and closed to accrual.
Job Duties include:
- Staff Management: Supervise the training/development and performance management for 6 direct and 5 indirect reports and responsible for the hiring of new staff.
- Protocol Development: Oversee all aspects of the protocol development process and other essential study document drafting.
- 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. Responsible for clinical trial budget development and invoicing.
- 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.
- At Least 4 years of clinical research experience.
- At least 2 years of direct staff management (preferred).
- 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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