Clinical Research Coordinator 100% Remote
As the worlds oldest and largest private cancer center, absolutely everything that we do is focused on changing the way that the world treats cancer. Research is integral to our mission at Memorial Sloan Kettering and clinical trials help us discover better forms of patient care and treatment. Our extraordinary scientists and clinicians work together to drive innovation and tackle some of the greatest challenges of biomedical science!
We are seeking Clinical Research Coordinators to join us in the fight against cancer. In this role, you will work collaboratively as a member of our research team focused on responsibilities related to managing clinical trials data. As a Clinical Research Coordinator, you will be an essential member of our team as data is the key to our research, allowing us to continuously learn about the people and diseases we help treat.
https://youtu.be/9R7QoNfmm0w
At Memorial Sloan Kettering, we have exciting opportunities for remote work , on-site 1-9 times per year!
You Are:
- A good decision-maker, with proven success at making timely decisions that keep the organization moving forward.
- Able to hold yourself and others accountable to achieve goals and live up to commitments.
- An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.
- Willing to take action and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.
- Resilient in recovering from setbacks and skilled at finding detours around obstacles.
- Passionate about medical terminology and science.
You Will:
- Collect, abstract, and enter data for research projects, databases, and/or protocols (clinical trials). This includes reviewing patient charts, existing databases, and other sources within a specified timeframe.
- Ensure data quality and integrity throughout the life of the study.
- Collaborate with members of the research and care teams across MSK regarding data input.
- Generate data reports and deliver to all necessary parties on the progress of the research project, database, or protocol.
- Design and/or enhance databases, data forms and tools (e.g. patient/human subject calendars, schedules, tracking logs) to facilitate patient consent and specimen collection as needed for assigned research projects.
- Ensure all appropriate Institutional, State, and Federal regulations throughout the study are followed.
- Provide clerical and administrative support, such as filing and scheduling meetings and appointments as needed.
You Have:
- A minimum of a High School Diploma, bachelors degree preferred
- Commitment for at least 2 years
Benefits:
Competitive compensation packages | Sick Time |Generous Vacation+ 12 holidays to recharge & refuel| Internal Career Mobility & Performance Consulting | Medical, Dental, Vision, FSA & Dependent Care|403b Retirement Savings Plan Match|Tuition Reimbursement |Parental Leave & Adoption Assistance |Commuter Spending Account |Fitness Discounts &Wellness Program | Resource Networks| Life Insurance & Disability |
We believe in communication, openness, and thinking beyond your 8-hour day @ MSK. Its important to us that you have a sense of impact, community, and work/life balance to be and feel your best.
Our Hiring Process
You review the posting, agree it sounds like a great fit & apply. If your profile aligns, our Talent Acquisition team will contact you to schedule a phone interview . After speaking with the Talent Acquisition Specialist, you will connect with the Hiring Manager by phone or video. If both you and the hiring manage feel the position is a fit, our Talent Acquisition team will perform reference checks, make an offer, and discuss onboarding and orientation.