Project Manager /Protocol Manager, Oncology Clinical Research - Odell Medical Search

Are you passionate about driving oncology clinical research forward and ensuring the highest standards of patient care? Do you thrive in a role where you can lead teams, implement strategic workflows, and make a tangible impact on healthcare innovation and cancer research? If so, we have an exciting opportunity for you in Northern, NJ.

Company Highlights - Why Choose Us? \

Join a prestigious healthcare network dedicated to advancing patient outcomes through cutting-edge clinical trials and research. Our organization is committed to quality, integrity, and innovation in healthcare, offering a supportive environment where your contributions are valued and recognized.

Employee Perks/Benefits

• • Comprehensive Health Benefits: Medical, dental, and vision coverage to keep you and your family healthy.
  • Retirement Plans: 401(k) with company match to help you plan for your future.
  • Professional Development: Opportunities for continuous learning and career advancement.
  • Work-Life Balance: Generous paid time off and flexible work schedules.
  • Wellness Programs: Access to fitness centers, wellness workshops, and mental health resources.

Community and Location Selling Points

• Nestled in the heart of New Jersey, Bergen County offers a perfect blend of suburban tranquility and urban excitement. With its close proximity to New York City, you can enjoy world-class dining, entertainment, and cultural experiences just a short drive away.
• Bergen County itself boasts beautiful parks, excellent schools, and a strong sense of community. Whether you enjoy hiking, shopping, or attending local sporting events, there’s something for everyone here.
• Plus, the cost of living is more affordable compared to neighboring metropolitan areas, making it an ideal place to live and work.

Role Overview

• As a Project Manager of Oncology Clinical Research, you will play a pivotal role in overseeing and driving the oncology clinical research trials conduct process within our Research Program.
• You will collaborate closely with investigators and research staff to develop and implement comprehensive workflows and procedures that ensure compliance with regulatory standards and optimize study efficiency.
• From protocol feasibility to study close-out, you will lead efforts to streamline processes, enhance data quality, and facilitate timely trial completion.

Key Responsibilities:

• Develop and implement workflows and Standard Operating Procedures (SOPs) for clinical trial conduct
• Ensure compliance with quality standards and regulatory requirements
• Coordinate protocol feasibilities, site selection, and startup processes
• Serve as a Super User for clinical trial management systems and electronic medical records
• Provide regular reports on study progress and challenges to Principal Investigators
• Foster relationships with stakeholders including investigators, sponsors, and regulatory agencies

Qualifications/Background Experience

• Bachelor's degree in a science or healthcare field
• Minimum of 8 years' experience in clinical research with progressive responsibilities
• Strong attention to detail and customer service focus
• Excellent organizational, communication, and interpersonal skills
• Proficiency in Microsoft Office and/or Google Suite
• Certification in Clinical Research (e.g., SoCRA, CCRA, or similar) preferred
• Project Management Professional (PMP) certification a plus

Why Join Us? Join a team that values innovation, collaboration, and patient-centric care. We offer a supportive work environment where your contributions are recognized and rewarded. Make a difference in healthcare and advance clinical research with us!

Ready to Make an Impact? If you're ready to take your career to the next level and make a meaningful difference in clinical research, we want to hear from you! Apply now and become part of our dedicated team.