Full Job Description
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 30th 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 2019, as well as one of Glassdoor’s Employees’ Choice Best Place to Work for 2019. We’re treating cancer, one patient at a time. Join us and make a difference every day.
We are seeking a Clinical Research Manager (CRM) for the Neurology department. The CRM serves as an integral member of the research team and will Implement standard for research protocol management, policies and procedures to ensure the highest quality management of clinical research studies.
The CRM serves as an integral member of the research team and will own the daily operations and activities of the program.
This is an excellent leadership opportunity within our growing clinical research team.
The CRM will be responsible for the following:
Staff Management: You will supervise the training/development and performance management for a large number of direct and indirect reports throughout the service.
Protocol Development: Lead aspects of the protocol development process including but not limited to preparing protocols, consent and other essential study document review.
Financial Management: Work closely with the appropriate partners, forecast trial resource needs, and assess staffing resource needs for program and senior leadership to ensure appropriate line function allocations
Clinical Trial Reporting: Generate protocol portfolio status reports for key partners. Implement 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 and ensure preparedness in routine audits for data quality, regulatory compliance, patient safety issues related to clinical trial. Communicate and ensure compliance with company policies and procedures, quality standards and improvement initiatives.
At least 4 years of clinical research experience.
2 years or more of direct staff management experience.
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 oal presentation skills required. Excellent interpersonal, leadership, decision-making and issue resolution skills are essential. #LI-POST
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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