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Associate Director, Operations – Clinical Assessment Technologies
Worldwide Clinical TrialsAssociate 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 & technologiesPMP
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
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
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