Global Clinical Lead

Job not on LinkedIn

🕒 July 22

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 28%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Lead global clinical operations strategy and execution for assigned clinical trials • Drive study startup including site selection, monitoring strategy, and operational planning • Coordinate cross functional teams across geographies ensuring alignment on timelines quality and deliverables • Monitor study progress including recruitment retention data quality and timelines and take corrective action when needed • Identify risks early and implement mitigation and contingency plans • Provide leadership direction and performance feedback to project team members • Function as primary point of contact for sponsors on clinical operations topics • Ensure compliance with ICH GCP regulatory requirements and internal processes • Oversee maintenance and quality of study documentation and central files • Support audits inspections and study closeout activities including database lock and archiving • Provide strategic oversight of the integrated data delivery (IDD) framework and champion a proactive data-quality culture

🎯 Requirements

• Degree in life sciences, nursing, or equivalent clinical research experience • Minimum of 5 years of experience leading clinical operations within a CRO environment • Proven experience in roles such as Clinical Trial Manager, Clinical Project Manager or Clinical Operations Leader • Experience leading complex global or multi-region studies • Strong knowledge of ICH GCP regulatory requirements and clinical trial processes • Experience coordinating cross functional teams and managing study timelines budgets and quality • Proficiency with clinical systems and standard tools such as CTMS, EDC, and eTMF • Strong leadership decision making and problem-solving skills • Demonstrated ability to lead global teams across cultures and time zones • Ability to prioritize competing demands and remain accountable for outcomes • A proactive mindset with strong ownership and sense of urgency • Excellent communication and stakeholder management skills • Comfort working in a fast-paced performance driven environment

🏖️ Benefits

• Additional incentives may be available based on performance and role scope