Remote Clinical Trial Job at Pfizer
Looking for a leadership role in clinical trial transparency, regulatory disclosure, and medical writing within a global pharmaceutical company? Pfizer is inviting applications for the position of Director, Clinical Trial and Data Transparency. This fully Remote Clinical Trial Job opportunity at Pfizer Careers is ideal for experienced professionals with expertise in regulatory medical writing, clinical trial disclosures, regulatory compliance, and data transparency. The role offers the opportunity to work on global clinical development programs while supporting transparency initiatives that advance patient trust and regulatory compliance.
About the Company:
Pfizer is one of the world’s leading biopharmaceutical companies dedicated to discovering, developing, and delivering innovative medicines and vaccines that improve patient outcomes globally. With a strong commitment to scientific excellence, research innovation, and healthcare advancement, Pfizer continues to address some of the world’s most challenging health conditions.
The company operates across multiple therapeutic areas and is recognized for its contributions to clinical research, regulatory science, and pharmaceutical innovation. Pfizer fosters a collaborative work environment that encourages professional growth, innovation, and global impact.
Job Details:
- Job Title: Director, Clinical Trial and Data Transparency
- Department: Medical Writing
- Location: India (Remote) / United Kingdom (Remote)
- Employment Type: Full-Time
- Work Mode: Fully Remote
- Job Requisition ID: 4956354
- Experience Required: Extensive experience in pharmaceutical, biotechnology, regulatory medical writing, or clinical disclosure functions
- Travel Requirement: Approximately 5%
Key Responsibilities:
- Develop and implement global strategies for clinical trial transparency and disclosure.
- Ensure compliance with international disclosure regulations and company policies.
- Manage disclosure activities for protocols, statistical analysis plans, clinical study reports, and clinical summaries in this Remote Clinical Trial Job.
- Drive quality, consistency, and timely completion of disclosure submissions.
- Oversee external vendors supporting disclosure-related deliverables.
- Forecast, monitor, and track outsourced disclosure projects at Pfizer Careers.
- Act as the primary liaison between Pfizer and disclosure vendors.
- Lead process improvements and technology implementation initiatives.
- Represent Medical Writing in clinical trial disclosure governance committees.
- Stay updated on evolving regulatory requirements, industry trends, and best practices.
Educational Requirements for this Remote Clinical Trial Job:
- Bachelor’s Degree in Life Sciences, Medical Sciences, Pharmacy, Biotechnology, or a related field.
- Master’s Degree (MS/MA) in a relevant discipline.
- PhD in Life Sciences, Medical Sciences, Pharmacy, Biotechnology, or a related field.
Experience Required:
- Extensive experience in the pharmaceutical or biotechnology industry.
- Strong background in regulatory medical writing.
- Experience preparing EMA Policy 70 submissions.
- Experience with clinical trial disclosure processes and regulatory documentation.
- Knowledge of clinical data transparency regulations.
- Experience working with cross-functional global teams.
- Vendor management and project leadership experience.
Skills Required:
- Clinical Trial Transparency and Disclosure Expertise.
- Regulatory Medical Writing.
- Project and Program Management.
- Regulatory Compliance Knowledge.
- Vendor and Stakeholder Management.
- Strategic Planning and Execution.
- Data and Document Anonymization Knowledge.
- Communication and Negotiation Skills.
- Change Management.
- Problem-Solving and Analytical Thinking.
- Cross-Functional Collaboration.
- Leadership and Team Influence.
Regulatory Knowledge Preferred:
Candidates with experience in the following regulations will have an advantage:
- EMA Policy 70
- EU Clinical Trial Regulation (EU CTR)
- Health Canada Public Release of Clinical Information Guidance
- Global Clinical Disclosure Regulations
- Pharmaceutical Industry SOPs and Compliance Frameworks
Benefits of the Remote Clinical Trial Job:
- Fully remote international work opportunity.
- Leadership role within a global pharmaceutical organization.
- Exposure to global clinical development programs.
- Opportunity to influence clinical transparency strategies.
- Collaboration with international medical writing and regulatory teams.
- Professional growth in regulatory science and clinical disclosures.
- Work on innovative technologies and process improvements.
- Inclusive and diverse workplace culture.
