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Director Clinical Operations Cro Jobs (NOW HIRING)

Director, Clinical Operations - Oncology We are seeking a strong, experienced Clinical Operations ... Provide effective CRO oversight by setting clear expectations, building productive partnerships ...

Director, Clinical Operations - Oncology We are seeking a strong, experienced Clinical Operations ... Provide effective CRO oversight by setting clear expectations, building productive partnerships ...

Director, Clinical Operations - Oncology We are seeking a strong, experienced Clinical Operations ... Provide effective CRO oversight by setting clear expectations, building productive partnerships ...

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Director Clinical Operations Cro information

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$146K

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How much do director clinical operations cro jobs pay per year?

As of Sep 8, 2026, the average yearly pay for director clinical operations cro in the United States is $145,969.00, according to ZipRecruiter salary data. Most workers in this role earn between $102,000.00 and $173,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Director Clinical Operations Cro jobs?

For Director Clinical Operations Cro jobs, the most frequently searched job titles are:

Director, Clinical Operations

Stoughton, MA • On-site

Scorpion Therapeutics
51 - 200 employees

$200 - $250/hr

Other

Posted 10 days ago


Job description

Position Overview:

This position is responsible for the strategic planning, financial oversight, and end-to-end execution of clinical trials while ensuring compliance with regulatory, quality, and internal standards. Oversees CROs and external vendors, manages cross-functional study teams, supports data integrity, and drives operational efficiencies to deliver studies on time, within approved budgets, and with high quality.

Responsibilities:
  • Formulate operational execution strategies for Phase I–IV clinical programs.
  • Own operational delivery from protocol development through completion of the clinical study report.
  • Develop and maintain integrated study timelines and milestones.
  • Identify and mitigate clinical trial risks with corrective actions.
  • Drive site selection and patient recruitment strategies.
  • Determine drug supply assumptions and ensure adequate drug supply at sites.
  • Lead identification, selection, and oversight of CROs/external vendors/trial sites.
  • Serve as primary oversight contact for CRO and vendor partnerships.
  • Lead contract and budget negotiations for clinical vendors.
  • Track CRO/vendor metrics and performance; manage clinical trial budgets and forecast costs.
  • Develop/review clinical protocols, investigator brochures, clinical development plans, and regulatory submission components.
  • Ensure study documents (plans, CRFs, listings/tables/figures, study reports) are accurate, complete, and aligned with objectives and regulations.
  • Ensure compliance with GCP/ICH/FDA and applicable requirements.
  • Maintain inspection readiness for trial master files and study documentation.
  • Lead development/review of clinical SOPs and operational processes.
  • Collaborate as a core member of cross-functional study teams; provide guidance/mentoring to partners and study team members.
  • Ensure seamless internal/external communication with CROs and trial sites.
Qualifications:
  • B.A. or B.S.; at least 8 years of clinical trial experience in pharma/biotech, including leading/overseeing clinical trial execution.
  • In-depth clinical operations expertise; knowledge of FDA regulations and ICH-GCP.
  • Expertise in budgeting, financial tracking, and contract negotiation.
  • Strong organizational, problem-solving, and operational management skills.
  • Effective verbal and written communication across organizational levels.
  • Proven cross-functional collaboration.
  • Flexibility to adapt to changing needs.
  • Proficiency with Microsoft Office (Excel, Outlook, PowerPoint, Word) and EDC systems.

Pay Range: $215,000 USD - $253,000 USD

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