⏳ Last Date to Apply: Not Specified
Parexel Global Clinical Operations Leader Recruitment 2026: Apply Online
Global Clinical Operations Leader / Clinical Trial Manager
Job Overview
Parexel International is a premier global clinical development partner dedicated to delivering insights-driven clinical and consulting solutions across the biopharmaceutical and life sciences industries. With a global team exceeding 22,000 employees, Parexel works with speed, agility, and a clear patient-first focus to accelerate the delivery of novel, life-saving therapies worldwide.
About the Role
As a Global Clinical Operations Leader / Clinical Trial Manager, you will take full ownership of the clinical operations strategy and operational execution of complex global clinical trials. Operating in a highly visible leadership capacity, you will ensure trials are delivered on schedule, within allotted budgets, and according to rigorous quality and regulatory compliance standards.
This role serves as the central clinical bridge connecting internal cross-functional contributors and biopharmaceutical sponsor teams across multiple geographic regions and time zones. Ideal candidates are strong decision-makers who excel in dynamic global settings and bring a proven track record of clinical trial delivery inside a Contract Research Organization (CRO).
Key Operational Impact Areas
- Operational Excellence: Strategic planning from study startup, site activation, and recruitment monitoring to final database lock.
- Sponsor Partnership: Serving as the key clinical point of contact, ensuring strategic alignment on milestones and deliverables.
- Risk Mitigation: Early identification of clinical risks and proactive implementation of contingency strategies.
- Compliance & Quality: Safeguarding strict adherence to ICH GCP guidelines, local regulatory rules, and integrated data quality delivery frameworks.
Key Job Details
| Company Name | Parexel International |
| Job Role | Global Clinical Operations Leader / Clinical Trial Manager |
| Experience | Minimum 5 years of experience leading clinical operations within a CRO environment |
| Salary Range | Competitive base pay aligned to experience level and location |
| Job Type | Full Time |
| Work Mode | Full-Time / Flexible |
| Openings | Not Specified |
| Job Location | Raleigh, North Carolina, United States |
Key Responsibilities
- Lead global clinical operations strategy and trial execution for assigned clinical studies.
- Drive study startup, site selection, monitoring framework, and operational planning.
- Coordinate cross-functional regional teams to ensure alignment on quality, timelines, and sponsor deliverables.
- Monitor recruitment, subject retention, data quality, and milestone timelines, executing corrective actions as needed.
- Identify operational risks early and execute mitigation and contingency strategies.
- Provide operational guidance, leadership, and performance feedback to project team members.
- Act as the primary clinical point of contact for pharmaceutical and biotech sponsor teams.
- Ensure full regulatory compliance with ICH GCP and internal Parexel quality systems.
- Oversee central study documentation, trial master files (eTMF), and maintain audit readiness.
- Support regulatory audits, sponsor inspections, database locks, and trial archiving activities.
Requirements & Qualifications
- Degree in life sciences, nursing, or equivalent clinical research background.
- Minimum of 5 years of clinical operations leadership experience in a CRO setting.
- Proven record in roles such as Clinical Trial Manager, Clinical Project Manager, or Clinical Operations Leader.
- Demonstrated experience directing complex global or multi-region clinical studies.
- Strong knowledge of ICH GCP guidelines, clinical trial procedures, and regulatory standards.
- Experience managing study budgets, timelines, and cross-functional regional teams.
- Proficiency with clinical trial systems including CTMS, EDC, and eTMF.
- Preferred expertise in therapeutic areas such as Metabolic, Obesity, MASH, Ophthalmology, or Dermatology / Immunology.
Required Skills
- Global Clinical Trial Leadership & Strategy
- Cross-Functional Team Coordination
- ICH GCP Regulatory Compliance
- Clinical Risk Assessment & Mitigation
- CTMS, EDC, and eTMF Systems Management
- Sponsor & Stakeholder Relationship Management
- Budgeting, Timeline Tracking, and Milestone Management
About Parexel International
Parexel International is a leading global clinical research organization (CRO) providing comprehensive clinical development services, consulting, and technological solutions to biopharmaceutical companies worldwide. Operating in over 80 countries, Parexel prioritizes patient well-being and clinical excellence through innovative research, inclusive culture, and collaborative teamwork.
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Frequently Asked Questions
Frequently Asked Questions
Q1: What is the primary role of a Global Clinical Operations Leader at Parexel?
A1: The role involves leading the operational strategy, trial execution, budget management, timelines, quality standards, and sponsor communications for global clinical trials.
Q2: What qualification is required?
A2: A degree in Life Sciences, Nursing, or an equivalent field with a minimum of 5 years of CRO clinical leadership experience is required.
Q3: Is prior CRO experience mandatory?
A3: Yes, candidates must have a proven history of delivering clinical trials within a Contract Research Organization (CRO) environment.