Life Science Jobs at Pfizer | Candidates Apply Now
Are you looking for Life Science Jobs, Pfizer Careers, or exciting Clinical Trial Jobs that offer remote work opportunities? Pfizer is hiring a Director, Clinical Trial and Data Transparency to support global clinical trial disclosure activities. This is an excellent opportunity for experienced life science professionals to work with one of the world’s leading pharmaceutical companies while contributing to regulatory transparency and compliance in clinical research.
About Pfizer
Pfizer is one of the world’s leading biopharmaceutical companies dedicated to discovering, developing, manufacturing, and delivering innovative medicines and vaccines. The company focuses on improving patient health through scientific research, regulatory excellence, and global healthcare solutions. Pfizer offers rewarding career opportunities for professionals seeking growth in clinical research, regulatory affairs, medical writing, and life sciences.
Job Details
- Position: Director, Clinical Trial and Data Transparency
- Company: Pfizer
- Job Type: Full-Time
- Location: India – Remote / United Kingdom – Remote
- Work Mode: Remote
- Department: Medical Writing
Key Responsibilities
- Provide subject matter expertise to teams to develop global strategies for the disclosure of clinical documents in accordance with applicable regulatory requirements.
- Support compliance with EMA Policy 70, EU Clinical Trial Regulation, Health Canada Public Release of Clinical Information Guidance, and company policies/SOPs.
- Manage planning and preparation activities for disclosures.
- Drive quality in information, consistency across disclosures and related areas, and completion of disclosures in a timely manner.
- Oversee vendors assigned to disclosure deliverables.
- Forecast and track outsourced disclosure deliverables.
- Act as the Pfizer point of contact to vendors and participate in governance meetings.
- Promote open communication regarding project status and issue resolution.
- Lead development of standard processes and implementation of technological solutions to ensure compliance with disclosure requirements.
- Represent Medical Writing on clinical trial disclosure governance committees.
- Maintain knowledge of regulatory guidelines, industry trends, and best practices.
Qualifications
Basic Qualifications
- Bachelor’s degree or equivalent in a medical-related field or life science.
- Post-graduate degree preferred.
- BS/BA with extensive experience, MS/MA with strong experience, or PhD with strong relevant experience in the pharmaceutical or biotech industry.
- Experience with regulatory medical writing and preparation of EMA Policy 70 submissions required.
- Knowledge of data and/or document anonymization strongly preferred.
Preferred Qualifications
- Advanced degree (MS/MA) preferred.
- Strong knowledge of data and/or document anonymization.
Experience Required
- Extensive experience in the pharmaceutical or biotechnology industry.
- Experience in regulatory medical writing.
- Experience preparing EMA Policy 70 submissions.
- Experience managing multiple projects simultaneously.
- Experience working with cross-functional global teams.
- Experience overseeing external vendors and disclosure deliverables.
Skills Needed
- Excellent project management skills.
- Strong interpersonal and communication skills.
- Negotiation and stakeholder management abilities.
- Ability to establish and maintain productive working relationships.
- Strong problem-solving skills.
- Ability to apply knowledge and experience to solve complex challenges.
- Flexibility and persistence in achieving project objectives.
- Change management and strategic planning skills.
Work Schedule & Travel Requirements
- Approximately 5% travel across GPD sites for face-to-face meetings when necessary.
- May need to accommodate global teleconference calls across different time zones.
- Remote work location assignment.
This Pfizer Careers opportunity is ideal for experienced professionals seeking advanced Life Science Jobs and Clinical Trial Jobs in a global pharmaceutical environment. With a fully remote work model, exposure to international regulatory frameworks, and the opportunity to contribute to clinical trial transparency initiatives, this role offers an excellent career pathway for life science and pharmaceutical professionals.
