# Senior Project Lead / Associate Director, Clinical Trial Management

**Company**: IQVIA
**Work arrangement**: remote
**Experience**: senior
**Salary**: $93,100.00 - $295,500.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/Trial-Delivery-Manager--Sponsor-Dedicated_R1570300?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_e6f9f7fd-d20

## Description

IQVIA is seeking an accomplished Senior Project Lead / Associate Director, Clinical Trial Management to provide centralized, global clinical trial oversight within our Functional Service Provider (FSP) model.

This role partners closely with a Global Trial Leadership and cross-functional stakeholders to ensure the successful planning, execution, and delivery of complex clinical trials across regions and vendors.

You will lead Study Management Teams (SMTs), oversee country and site-facing activities, and ensure trials are conducted with the highest standards of quality, compliance, and inspection readiness,from start-up through close-out.

**Key Responsibilities**

- Global & Regional Trial Leadership:

+ Lead and coordinate global and regional clinical trial management activities for internally managed and outsourced studies.   + Serve as a core member of the Trial Team, partnering with Global Leadership to deliver operational strategy and execution.   + Act as primary point of contact for country, regional, and functional stakeholders within Clinical Development Operations.   + Function as backup or first point of contact in the absence of the Global Leadership.

- Central Trial Oversight & Execution:

+ Drive trial delivery across the full lifecycle: feasibility, site selection, start-up, execution, and close-out.   + Ensure milestones, timelines, and deliverables are met and transparently communicated.   + Maintain real-time trial oversight through dashboards, reports, and issue tracking.   + Act as the central subject matter expert for assigned protocols.

- Vendor & Partner Management:

+ Provide oversight of CROs and global vendors supporting site-facing activities.   + Review and approve vendor deliverables, invoices, and spend.   + Ensure vendor performance aligns with trial plans, budgets, and quality expectations.

- Quality, Compliance & Inspection Readiness:

+ Ensure continuous inspection readiness in accordance with ICH-GCP, applicable regulations, and sponsor SOPs.   + Lead or contribute to CAPA development and resolution.   + Support Health Authority inspections, internal audits, and quality reviews.

- Enrollment, Feasibility & Risk Management:

+ Lead feasibility activities and provide data-driven recommendations.   + Establish and track regional enrollment commitments, ensuring alignment with projections.   + Ensure robust recruitment and contingency plans are in place.   + Proactively identify risks, escalate issues, and drive resolution.

- Documentation, Systems & Trial Deliverables:

+ Oversee trial documentation, filing, archiving, and retention.   + Create, review, and maintain trial-specific documents.   + Support HA/EC/IRB submissions with required central documents.   + Coordinate data cleaning activities to support timely database lock.

- Leadership, Mentorship & Continuous Improvement:

+ Lead teams across projects or programs.   + Provide coaching and mentoring to less experienced team members.   + Lead or participate in special initiatives, task forces, and process improvement efforts.   + Contribute innovative ideas to enhance operational efficiency and quality across the FSP partnership.

**Qualifications & Experience**

- Education: Bachelor’s degree (or equivalent) in Life Sciences (e.g., Biology, Chemistry, Nursing, Pharmacy).

- Experience: 6+ years of clinical trial management experience in pharma and/or CRO environments.

- Technical & Professional Skills:

+ Deep knowledge of ICH-GCP, regulatory requirements, and clinical operations best practices.   + Strong project management, planning, and risk mitigation skills.   + Demonstrated ability to manage country and vendor budgets.   + Experience with CTMS, TMF systems, and Microsoft applications.   + Strong analytical, decision-making, and communication skills.   + Fluent in English; local language proficiency as required.

**Salary:** The potential base pay range for this role, when annualized, is $93,100.00 - $295,500.00.

## Skills

### Required
- ICH-GCP
- CTMS
- TMF systems
- Microsoft applications
- English

### Nice to have
- monitoring experience
- Therapeutic area experience

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Durham-North-Carolina-United-States-of-America/Trial-Delivery-Manager--Sponsor-Dedicated_R1570300?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)