Global Biometrics Delivery Lead

🔥 0 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟠 Senior

👻 Ghost score 10%

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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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 the execution of Data Operations strategy and Data Operations technology setup for assigned projects and programs • Serve as the primary point of contact for Global Data Operations activities, partnering with clients, functional leaders, and project stakeholders • Provide leadership across database programming, data integration, data management, and statistical services teams across multiple geographies • Create and execute project timeline plans covering Global Data Operations deliverables and coordinate dependencies across Data Management, Programming, and Biostatistics • Manage project budgets, resource planning, and staffing requirements while monitoring productivity and project progress • Ensure project activities comply with quality standards, SOPs, ICH-GCP requirements, and applicable regulatory guidelines • Identify project risks proactively and contribute to risk mitigation planning and resolution • Support project startup, study conduct, closeout activities, audits, inspections, and project documentation maintenance • Collaborate with study teams and Data Standards Associates to support applicable data standards • Establish working relationships with functional experts and provide leadership, guidance, and project direction • Monitor scope, timelines, deliverables, and project metrics to ensure contractual commitments and business objectives are achieved • Drive continuous improvement initiatives and contribute to operational excellence across project delivery activities

🎯 Requirements

• Bachelor's degree in a science or industry related discipline, or equivalent qualification • Demonstrated application of project management concepts • Proven experience leading project teams in a technical, programming, data management, or statistical environment with minimal supervision • Understanding of cross functional clinical development activities • Knowledge of SOPs, ICH-GCP guidelines, and applicable local and international regulations • Strong written and verbal English communication skills • Ability to work effectively within global and culturally diverse teams • 10+ Experience supporting data management, statistical programming, data integration, or biometrics functions within clinical development • Understanding of clinical trial systems and how technology platforms support Data Operations delivery • Experience participating in audits, inspections, or quality improvement initiatives • Knowledge of clinical data standards and their application within clinical trials • Ability to travel domestically and internationally as needed

🏖️ Benefits

• Remote work arrangement • Opportunity to influence clinical trial delivery and support innovative therapies • Collaborative, fast-paced work environment • Global and culturally diverse team environment • Opportunities to contribute to continuous improvement and operational excellence