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Worldwide Clinical Trials

Associate Director, Operations – Clinical Assessment Technologies

Worldwide Clinical Trials

Associate Director managing operations for Clinical Assessment Technologies at Worldwide Clinical Trials. Identifying operational needs, managing resources, and ensuring project compliance.

Posted 6/25/2026full-timeRemote • North Carolina • 🇺🇸 United StatesSenior💰 $112,000 - $223,000 per yearWebsite

Tech Stack

Tools & technologies
PMP

About the role

Key responsibilities & impact
  • Identify operational needs for upcoming projects, track and review current assignments for CAT Operations staff
  • Resource CAT study projects as Resource Manager
  • Engage as Subject Matter Expert (SME) for CAT Operations activities
  • Provide operational oversight for designated CAT study projects
  • Engage in and coordinate resourcing activities for all CAT awarded projects
  • Identify training and skills gaps among staff; coordinate and assist with learning opportunities to enhance operations staff knowledge and skills of industry related regulations, processes, materials, and guidelines
  • Actively identify and engage in process improvement activities
  • Participate in QMD reviews and new QMD development
  • Author, collaborate, and review QMD documents and guidance documents
  • Coordinate and manage CAT Operations team meetings
  • Active engagement and oversight of study risk assessments, as they relate to operational activities
  • Work with department leaders to ensure alignment among CAT operational and clinical services
  • Lead and/or contribute to departmental initiatives that aim to implement policies, methods, techniques to contribute to existing service areas and department growth
  • Accountable for oversight of CAT study deliverables from Launch process to study close out
  • Assist and collaborate with Operations staff, Project Management, Contracts on vendor and study budget development, scope of work revisions, tracking and compliance
  • Assist in vendor management related concerns, including involvement with escalations, Vendor Management and Quality Assurance meetings
  • Review and assess ongoing budget utilization and revenue recognition with Operations Managers to ensure projects are meeting financial targets
  • Manage internal CAT operations meetings and other trial-specific meetings, as appropriate
  • Significant contributor to multiple strategic departmental, sponsor-related and cross-functional initiatives
  • Participate in business development activities including; but not limited to proposals input, capabilities, and bid defense meetings
  • Apply thorough knowledge of industry regulations and guidelines to ensure operational compliance during clinical trial conduct

Requirements

What you’ll need
  • Must have a minimum of a bachelor’s degree, preferably with an Master’s degree (life sciences, MBA and/or PMP certification)
  • Strong leadership, management and interpersonal skills
  • Strong planning and organizational skills
  • At least 7+ years clinical trial experience with at least 4 years’ experience in global clinical trials
  • Preferred at least 5+ years of experience managing team members or project management experience
  • Hands on experience in day-to-day management of all aspects of global clinical trials required
  • Prior experience in psychiatry / CNS therapeutic areas is a plus

Benefits

Comp & perks
  • Competitive benefits package depending on location
  • Pay equity and transparency

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
clinical trial managementproject managementbudget developmentrisk assessmentprocess improvementresource managementQMD document authoringvendor managementcompliance oversightstrategic initiative contribution
Soft Skills
leadershipinterpersonal skillsplanningorganizational skillscollaborationcommunicationoversighttraining coordinationteam managementproblem-solving
Certifications
PMP certificationMaster's degreeBachelor's degree