The Prostate Cancer Clinical Trials Consortium (PCCTC) is hiring a Project Manager (PM). In this role, you will be responsible for providing support to the Clinical Operations Program Manager for multi-center clinical research activities. Dedication to accuracy, high attention-to-detail, and the ability to work independently are critical competencies for the role. You will: - Manage staff and their development - Participate in the orientation, training and supervision of Clinical Research Coordinators and/or Project Associates. Participate in facilitating staff trainings. Align staff and resources with appropriate responsibilities and research needs. Maintain workflow consistency amongst staff with standardized processes.
- Manage and champion multi-institutional clinical research studies as required by the Sponsor.
- Design and oversee operations of clinical research studies including protocol and informed consent drafting, regulatory document drafting, project management, monitoring, and quality plan drafting, etc.
- Communicate effectively by establishing strong working relationships with a diverse matrix of stakeholders, including but not limited to study sites, investigators, pharmaceutical & biotechnology executives, executive committee members, and other important stakeholders.
- Synthesize complex clinical, regulatory, and other research study information into actionable plans.
- Provide necessary documentation in compliance with existing standard operating procedures, regulatory guidelines, etc.
- Assist in maintaining necessary research study conduct documentation (includes Project Management Plans, Safety Management Plans, Monitoring Plans, Meeting Minutes, etc.).
- Communicate and work effectively with all stakeholders of the PCCTC Executive Leadership, Clinical Operations, Data Management, Business Management, Budgets & Contracts, Editorial, etc.
You are: - 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.
You Have: - 4-7 years of relevant experience
- Proven track record of leading clinical research projects with deadlines.
- Knowledge and experience with clinical trial execution.
- Solid understanding of the Code of Federal Regulations, Good Clinical Practice, and Human Subjects Protection.
- Strong organizational, prioritization, and project management skills.
- Strong computing skills including proficiency in MS Office products.
- Ability to work productively in a remote work environment.
- Experience working with prostate cancer clinical trials and/or multicenter projects is a plus.
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 | Remote Flexibility 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 ->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. #LI-POST |
