Remote Clinical Trials Job at Pfizer, United Kingdom | Life Sciences Candidates, Apply Online

Remote Clinical Trials Job at Pfizer, United Kingdom | Life Sciences | Apply Online

If you are a seasoned medical writing executive or a clinical data privacy expert looking to step into a high-visibility global leadership position, this full-time role at Pfizer is an exceptional opportunity. Available as a fully remote position in both India and the United Kingdom, this director-level role sits at the critical intersection of clinical compliance, data privacy, and global regulatory submission strategy. For advanced professionals searching for a top-tier Clinical Trials Job, this position offers total strategic ownership over the public disclosure and anonymization of clinical trial data. It serves as an elite milestone for a long-term Pfizer career and stands out as a premier executive-level Clinical Research Job in the international pharmaceutical sector.

About The Company

Pfizer is one of the world’s premier biopharmaceutical companies, dedicated to discovering, developing, and manufacturing life-saving medicines and vaccines. Known for its relentless pursuit of scientific breakthroughs, Pfizer operates on a massive global scale, delivering therapies that alter the trajectory of human health. The Global Product Development (GPD) and Medical Writing departments at Pfizer ensure absolute transparency, data integrity, and strict alignment with international regulatory authorities, setting the industry benchmark for ethical data sharing and public clinical disclosure.

Clinical Trials Job – Key Responsibilities

As the Director of Clinical Trial and Data Transparency, you will serve as the principal subject matter expert within the Medical Writing department, driving the global strategy and operational execution for disclosing Pfizer-sponsored interventional trial documents.

Your core executive, vendor management, and governance duties will include:

• Global Disclosure Strategy: Developing and implementing comprehensive global strategies for the public disclosure of clinical regulatory documents (including protocols, Statistical Analysis Plans [SAPs], Clinical Study Reports [CSRs], and marketing overviews) to advance this Clinical Trials Job.
• Regulatory Compliance Frameworks: Enforcing absolute compliance with evolving international transparency mandates, including EMA Policy 70, the EU Clinical Trial Regulation (EU CTR), and Health Canada’s Public Release of Clinical Information (PRCI) guidance.
• Anonymization & Data Sharing: Overseeing complex qualitative and quantitative document and data anonymization workflows to protect patient privacy while maintaining scientific utility across public registries.
• Global Vendor Oversight: Managing external vendors assigned to disclosure deliverables. You will forecast outsourcing budgets, track key performance indicators (KPIs), develop metric scorecards, and lead vendor governance meetings.
• Technological Innovation: Leading the development of standardized internal processes and the integration of advanced technological solutions (such as AI-enabled redaction and tracking platforms) to maximize throughput and consistency across disclosures.
• Corporate Governance: Representing the Medical Writing division on cross-functional clinical trial disclosure governance committees, while mentoring internal teams on emerging industry trends and global best practices for this Clinical Research Job.

Qualifications & Profile Requirements For Clinical Trials Job

This senior-level leadership vacancy is tailored for highly articulate, matrix-vetted professionals who demonstrate a masterful command of clinical document life cycles and global health authority transparency requirements.

• Educational Foundation: At minimum, a Bachelor’s degree or equivalent in a life science discipline is required. A post-graduate advanced degree (MS/MA/PhD) is highly preferred to build a successful Pfizer career.
• Industry Experience Tracking:
  • Bachelor’s Holder: Extensive, long-term leadership experience within the pharmaceutical or biotechnology industry.
  • Master’s/PhD Holder: Strong, deeply relevant post-graduate experience operating within regulatory medical writing or data transparency sectors.
• Core Technical Expertise: Direct, hands-on experience with regulatory medical writing and the complete preparation of EMA Policy 70 submissions is mandatory.
• Data Privacy Acumen: A robust, proven understanding of data and document anonymization methodologies, redaction principles, and quantitative risk thresholds.
• Interpersonal & Project Skills: Exceptional project management habits to lead multi-center timelines, paired with advanced negotiation and communication skills to influence cross-functional peer networks and steering committees.

Logistics, Schedule & Global Environment

• Location & Assignment: 100% Remote (Available to candidates permanently residing within India or the United Kingdom).
• Schedule: Full-time, executive hours. Candidates must possess the flexibility to accommodate global teleconference calls across highly diverse international time zones.
• Travel Requirements: Occasional travel (~5%) across global Pfizer product development sites for face-to-face executive briefings and leadership workshops.
• Compliance Note: Applicants must adhere strictly to Pfizer’s candidate AI-use guidelines during the recruitment and evaluation process.

In short, the Director of Clinical Trial and Data Transparency position at Pfizer is a definitive route to translating your advanced regulatory writing background into a high-impact, global governance portfolio. Securing this role allows you to step away from localized document drafting and actively shape the corporate policies, vendor ecosystems, and technological solutions that dictate how the world’s largest clinical pipeline interacts with public data registries. If you possess a life sciences background, elite expertise in EMA Policy 70, and the drive to lead a remote global matrix team, apply today to secure this premier opportunity.

APPLY ONLINE HERE