Memorial Sloan-Kettering Cancer Center Project Associate, PCCTC in New York, New York
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. We’re treating cancer, one patient at a time.Join us and make a difference every day.
TheProstate Cancer Clinical Trials Consortium (https://pcctc.org/) (PCCTC) is hiring a Project Associate. In this role, you will be responsible for providing support to the Clinical Operations team for multi-center clinical trial activities from concept to close-out.
Manage complex multi-institutional clinical trials across a diverse research portfolio.
Assist in overseeing clinical trials including protocol and informed consent drafting, regulatory document drafting, etc.
Communicate effectively and establish strong working relationships with a diverse matrix of clinical trial sites, investigators, pharmaceutical & biotechnology partners, and other important stakeholders.
Sustain project workflows and timelines, ensuring deadlines and milestones are met.
Maintain comprehensive, GCP/FDA compliant, Trial Master Files for assigned projects. Manage regulatory approvals (ex. IRB), review and filing of documents for Trial Master Files for projects.
Synthesize complex clinical, regulatory, and other clinical trial information into actionable plans.
Provide necessary documentation in compliance with existing standard operating procedures, regulatory guidelines, etc.
Assist in maintaining necessary clinical trial conduct documentation (includes Project Management Plans, Safety Management Plans, Monitoring Plans, Meeting Minutes, etc.).
Communicate and work effectively with all stakeholders of the PCCTC - Clinical Operations, Data Management, Business Management, Budgets & Contracts, Editorial, etc.
Adept at planning and prioritizing work to meet commitments aligned with organizational goals.
An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.
Comfortable working in a fast-paced environment.
Adept at building partnerships and working collaboratively with others to meet shared objectives and goals.
A Bachelor's degree (preferred) with least 2-4 year of clinical research experience.
Proven ability to manage clinical research projects with strict deadlines.
Working knowledge of the Code of Federal Regulations, Good Clinical Practice, and Human Subjects Protection.
Knowledge of clinical trial regulatory and safety management preferred.
Strong computing skills including proficiency in MS Office products.
Ability to solve problems by using a logical, systematic, sequential approach.
Ability to work productively in a remote work environment.
Experience working with prostate cancer clinical trials and/or multicenter projects is a plus.
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 | Remote Flexibility
We believe in communication, openness, and thinking beyond your 8-hour day @ MSK. It’s 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 ->Talent Acquisition contacts you to schedule a phone interview (if your profile aligns) -> after speaking with the Talent Acquisition Specialist, you will connect with the Hiring Manager by phone or video -> if your experience is a fit, you will move forward to a video call or on-site visit with the team -> post-interview feedback->ideally an offer! ->reference check & onboarding-> orientation & official welcome to MSK.
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.
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.
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Job LocationsUSA-NY-New York
Posted Date1 week ago(5/7/2021 3:21 PM)
Requisition ID 2021-48221
Category Research - Clinical