Pay Range$25.65-$38.42Company 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. Please review important announcements about vaccination requirements and our upcoming EHR implementation by clicking here (https://careers.mskcc.org/frequently-asked-questions/) . Important Note for MSK Employees: Your Career 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 (https://mskcc.sharepoint.com/sites/pub-hr/SitePages/Career-Hub.aspx) to learn more. Please note, this link is only accessible for MSK employees. Job DescriptionExciting opportunity at MSK: Join our team as a Clinical Research Coordinator, Prostate Cancer Clinical Trials Consortium (PCCTC) ! We’re looking for a dynamic clinical research professional to work on data requests and management – data is key to our research, allowing us to continuously learn about the people and diseases we help treat. Role Overview:
Collect, abstract, and enter data for research projects, databases, and/or protocols (clinical trials).
Ensure data quality and integrity throughout the life of the study.
Collaborate with research and care teams across MSK regarding data input.
Generate data reports and deliver to all vital parties on the progress of the research project, database, or protocol.
Enter data into Design and/or improve databases, data forms and tools (e.g. schedules, tracking logs) to facilitate patient consent , data and specimen collection as needed for assigned research projects.
Ensure all appropriate Institutional, State, and Federal regulations throughout the study are followed.
Coordinate clinical research workflows and serve as the main point of contact, if applicable
Key Qualifications:
Healthcare/research experience a plus.
Core Skills:
Decision-making, with shown success at making timely decisions.
Ability to hold yourself and others accountable to achieve goals and live up to commitments.
Willing to take action and eager to embrace new opportunities and tough challenges.
Resiliency in recovering from setbacks and skilled at finding detours around obstacles.
Passion about medical terminology and science.
Excellent communication skills.
Enthusiasm and dedication to MSK's vision, mission and values.
Additional Information :
Location: Remote
Schedule: Full-time, Monday to Friday
Reporting to the Project Manager
Commitment for at least 2 years
Pay Range: $25.65 - $38.42
Helpful Links :
MSK Compensation Philosophy (https://careers.mskcc.org/frequently-asked-questions/)
Review our great benefits offerings
Learn more about PCCTC : The Prostate Cancer Clinical Trials Consortium (PCCTC) was initiated in 2005 by the Prostate Cancer Foundation (PCF) and the U.S. Department of Defense (DOD) Prostate Cancer Research Program (PCRP) in response to critically unmet needs in prostate cancer clinical research identified by physician investigators and patient advocates. To fulfill our mission, we developed a unique infrastructure which has fostered a culture of transparent project co-development between investigators, research sites and industry partners. Established as an independent entity in 2014, the PCCTC, LLC is now the nation’s premier multicenter clinical research organization specializing in cutting-edge prostate cancer research.
ClosingMSK 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 (https://externaltalent-mskcc.icims.com/connect?back=intro&iniframe=1&hashed=-435744324) to receive inside information on our organization and new job opportunities.Job LocationsUSA-NY-New YorkPosted Date19 hours ago(10/12/2024 1:37 AM)Requisition ID 2024-81030 Category Research - Clinical Pay Range $25.65-$38.42
Full-time- ID: #52689928
- State: New York New york city 00000 New york city USA
- City: New york city
- Salary: USD TBD TBD
- Showed: 2024-10-12
- Deadline: 2024-12-11
- Category: Et cetera