Director of Clinical Research Management - Oncology

System One Holdings, LLC

• $200K — $220K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree from an accredited college or university
  • 10+ years of relevant professional experience in oncology clinical research
  • Strong understanding of clinical research processes and site relationships
  • Excellent written and verbal communication skills
  • Organizational and project management skills to manage multiple priorities
  • Preferred: Management or supervisory experience
  • Preferred: SOCRA certification

Responsibilities

  • Provide leadership for oncology clinical research programs
  • Lead start-up activities including site identification and budget development
  • Develop relationships with investigative sites and clinical research partners
  • Collaborate with legal teams on contracts and program matters
  • Manage contracted CRO partners supporting programs
  • Supervise and support assigned personnel
  • Participate in client meetings and assist with RFP preparation

Benefits

  • Health and welfare benefits coverage options including medical, dental, and vision
  • Participation in a 401(k) plan
  • Life insurance and voluntary plans available
Full Job Description
Job Title: Director of Clinical Research Management - Oncology
Location: Philadelphia, PA
Type: Direct Hire - Full time permanent direct with our client
Compensation: $200,000.00 - $220,000.00
Work Model: Hybrid - remote with occasion in office meetings required
Hours: 40.0 hours per week

Are you ready to help shape the future of Oncology clinical research? We are seeking a seasoned clinical research leader to drive high-impact Oncology programs, build strategic partnerships across sponsors, CROs and investigative sites, and play a key role in advancing innovative cancer research. This is a highly visible leadership opportunity, for an experience professional who thrives at the intersection of clinical operations, program strategy, business development and stakeholder engagement.

Responsibilities

  • Provide leadership and oversight for oncology clinical research programs
  • Lead and support program start-up activities, including site identification and selection, budget development, and contract negotiations
  • Develop and maintain strong working relationships with investigative sites and other clinical research partners
  • Work directly with sites and collaborate with legal teams and clinical trial sponsors on contracts and related program matters
  • Provide management and oversight of contracted CRO partners supporting programs
  • Supervise and support assigned personnel
  • Contribute to the development of program documents, presentations, and other materials needed for successful program execution
  • Partner with the Vice President and business development team to develop company capabilities presentations and marketing materials
  • Participate in client meetings, proposal presentations, and proposal defense meetings
  • Assist with the preparation, review, and revision of scopes of work, RFP responses, contracts, and related business development materials
  • Present organizational capabilities to prospective and existing clients
  • Contribute to business development and marketing strategies that support the organization's clinical research programs
  • Represent the organization at major oncology and clinical research meetings and conferences, including ASCO and ONS
  • Travel to client locations and other business-related meetings as needed


Requirements

  • Bachelor's degree from an accredited college or university
  • 10+ years of relevant professional experience in oncology clinical research and/or communications
  • Experience working in clinical research operations and/or the clinical trial environment
  • Strong understanding of clinical research processes and investigative site relationships
  • Excellent written, verbal, presentation, and interpersonal communication skills
  • Strong organizational and project management skills, with the ability to manage multiple priorities and stakeholders
  • Proficiency with Microsoft Office and related business systems
  • Management or supervisory experience (preferred)
  • Master's degree in an appropriate discipline (preferred)
  • SOCRA certification (preferred)
  • Experience with business development, client presentations, proposals/RFPs, scopes of work, budgets, and contracts (preferred)
  • Experience working with investigative sites, clinical trial sponsors, CROs, pharmaceutical or biotechnology companies, academic research organizations, or cooperative groups (preferred)


System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

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Ref: #568-Clinical

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