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Governance, Risk and Compliance Project Manager

Job not on LinkedIn

🔥 5 minutes ago

🇮🇳 India – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

Where this job comes from

Posted on Worldwide Clinical Trials's careers page, not through a job board

First seen by Remote Rocketship 5 minutes ago

Logo of Worldwide Clinical Trials

Worldwide Clinical Trials

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Independently lead information security projects from initiation through closure • Define objectives, scope, deliverables, milestones, resource needs, success measures, and acceptance criteria • Convert security strategies, risk treatment plans, audit findings, regulatory commitments, and operational needs into executable project plans • Maintain schedules, action logs, decision records, risk and issue registers, budgets, status reports, and project documentation • Facilitate working sessions, remove obstacles, and follow through on commitments • Coordinate Information Security, Information Technology, Privacy, Legal, Quality, Vendor Management, Procurement, Clinical Operations, and other business functions • Engage with security architects, engineers, analysts, and technology owners to keep delivery on track • Identify and manage delivery and security risks, issues, dependencies, mitigation actions, and escalations • Ensure projects follow Office of the CISO governance, security, privacy, quality, change-management, and documentation requirements • Coordinate reviews, approvals, evidence, and readiness activities before implementation • Provide updates on progress, decisions, risks, financials, and expected outcomes to executives and stakeholders • Translate security and technology matters into practical business terms within a clinical research organization • Coordinate third parties supporting security initiatives, including deliverables, dependencies, performance, security obligations, and issue resolution • Plan stakeholder engagement, communications, training, implementation readiness, and transition to operations • Maintain project data and contribute to portfolio dashboards, capacity planning, prioritization, and leadership reporting • Apply lessons learned and improve project management practices, templates, and standards • Perform other duties as assigned

🎯 Requirements

• Bachelor’s degree in information security, cybersecurity, information technology, business, project management, or a related field; an equivalent combination of education and directly relevant experience may be considered • Five or more years of project management experience, including independently delivering multiple information security or cybersecurity projects through completion • Documented experience managing security initiatives such as identity and access management, vulnerability remediation, security tooling, cloud security, data protection, third-party risk, security operations, compliance remediation, or security transformation • Working knowledge of core information security concepts and common enterprise technology environments • Ability to understand architecture diagrams, technical requirements, control designs, testing results, and implementation plans • Experience leading cross-functional teams and vendors through planning, execution, implementation, and transition to operations in a matrixed organization • Strong command of project management practices, including scope, schedule, budget, resources, risks, issues, dependencies, change control, governance, and benefits tracking • Excellent written, verbal, facilitation, and presentation skills • Experience preparing executive-level status reports and decision materials • Proficiency with project planning, collaboration, reporting, and presentation tools • Experience developing portfolio metrics and dashboards is preferred • Experience in a clinical research organization, life sciences, healthcare, pharmaceutical, or another regulated environment is strongly preferred • PMP, PRINCE2, Certified ScrumMaster, or comparable project management certification is preferred • Security certification such as CISSP, CISM, Security+, or equivalent is beneficial

🏖️ Benefits

• Collaborative and inclusive environment • Growth and professional development opportunities • Opportunity to learn, grow, and help shape the future of clinical research

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