What are the responsibilities and job description for the Project Manager I, Regulatory & Scientific Affairs position at CTI Clinical Trial and Consulting Services?
Job Summary: Primarily responsible for overseeing and coordinating the operational aspects of safety/data monitoring committee projects ensuring quality, timeliness and client satisfaction and will manage all phases of additional client projects from planning to completion.
What You'll Do
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com
Why CTI?
In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.
Please Note
What You'll Do
- In conjunction with RSA Directors and Medical Writers, specific tasks or duties may include, with anticipated oversight from Manager, RSA:
- Plan: Create timelines and project needs assessments
- Coordinate: Organize resources to develop the project, including multifunctional project team, budget, external vendors, etc.; manage timelines
- Implement: Produce or oversee timely production of quality deliverable, on budget
- Problem Solve: Identify challenges that arise and propose effective solutions
- Finalize for Client/Senior Management: Oversight of final review and production of deliverables
- Provide project status reports to client and management
- Prioritize and manage resources to meet needs of several clients simultaneously with main project load expected in resident region
- Lead internal or external meetings with anticipated oversight from Manager, RSA
- Effective communication and professional interaction with client and internal team ensuring client’s expectations are met
- Bachelor’s degree in allied health field such as nursing, pharmacy, or health/natural science or an equivalent combination of education and relevant work experience.
- At least 3 years clinical or business background in drug or device research/development, biotechnology, pharmaceutical or clinical research and/or combination of education & experience
- Experience with drug development process and/or medical writing preferred
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com
Why CTI?
- Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
- Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
- Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.
In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.
Please Note
- We will never communicate with you directly via Microsoft Teams Messaging or by text message
- We will never ask for your bank account information at any point during the recruitment process