Position: Associate Clinical Project Management Director / Trial Delivery Manager (TDM) – Cross Therapeutic Areas
📍 Location: Parsippany, New Jersey (Remote/Home-based, with potential travel)
🕒 Employment Type: Full-Time
💼 Job ID: R1506570
🌐 Additional Locations: Remote, North Carolina, Pennsylvania, New Jersey
About IQVIA
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, accelerating the development and commercialization of innovative medical treatments.
🔗 Learn more: https://jobs.iqvia.com
Position Overview
The Associate Clinical Project Management Director / TDM leads and coordinates global and regional clinical trial management activities. This role ensures successful planning, execution, and closure of clinical trials, whether internally managed or outsourced.
The TDM is a key member of the Study Management Team (SMT), collaborating with internal and external stakeholders to ensure compliance, quality, and timely delivery of trial milestones.
Key Responsibilities
1. Trial Oversight & Management
Lead the Study Management Team and provide regular updates on trial deliverables.
Track trial progress in real-time and maintain inspection-readiness.
Act as the primary contact for country/regional staff and internal teams.
Partner with Global Trial Leads to manage trial activities from start-up to close-out.
Escalate and resolve trial issues; contribute to CAPA processes.
2. Site & Vendor Coordination
Support site selection and feasibility assessments.
Monitor enrollment commitments and recruitment plans.
Oversee vendors and review deliverables and invoices.
Coordinate with vendors (IVRS, Central Labs, ePRO, Imaging, Translation, Ancillary Supplies).
3. Documentation & Compliance
Create and maintain trial-specific documents (Monitoring Guidelines, ICFs, Blinding Plans).
Ensure timely filing, archiving, and retention of trial documents.
Provide central documents for regulatory submissions.
Support Health Authority inspections and internal audits.
4. Training & Meetings
Develop and deliver trial-specific training materials.
Coordinate and participate in Investigator Meetings.
5. Budget & Financial Oversight
Establish country budgets and monitor actuals vs. forecast.
Understand Out-of-Pocket (OOP) and FTE cost drivers.
Qualifications
Education:
Bachelor’s degree in Life Sciences (Biology, Chemistry, Biochemistry, Nursing, Pharmacy) or equivalent.
Experience:
Level 2 (Advanced): Minimum 8 years of experience with leadership in complex trials at a large pharmaceutical company.
Skills & Competencies:
Strong knowledge of ICH-GCP and local regulatory requirements.
Proven ability to lead cross-functional teams and manage global trials.
Excellent communication, decision-making, and analytical skills.
Proficiency in Microsoft Office, CTMS, TMF, and other clinical systems.
Experience in virtual team coordination and stakeholder engagement.
Ability to manage ambiguity and drive solutions proactively.
Preferred Attributes:
Monitoring or data management experience.
Budget planning and financial oversight experience.
Ability to mentor junior CTMs and lead special initiatives or task forces.
Therapeutic area expertise and protocol knowledge.
Metrics & KPIs
Performance measured according to the Quality Oversight Plan (QOP) and trial-specific deliverables.
Compensation & Benefits
Base Pay Range (annualized): $93,100 – $285,500
Actual base pay may vary based on qualifications, experience, location, and schedule
Eligible for incentive plans, bonuses, and additional benefits depending on the position
Equal Opportunity Employer
IQVIA provides employment consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected status.
🔗 Equal Opportunity Statement
📩 Apply Now: IQVIA Careers – Associate Clinical Project Management Director
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