Are you an organized professional with a knack for detail and a passion for pharmacovigilance? PPD, a global leader in clinical research, is hiring a Safety Administrator to join their Global Safety Writing Team. This fully remote position, based in India or Philippines, offers a unique opportunity to contribute to critical safety-related documents like aggregate safety reports, regulatory responses, and Risk Management Plans (RMPs). If you thrive in a fast-paced environment and excel at multitasking, this role is for you. Read on to explore the responsibilities, qualifications, benefits, and how to apply for this exciting pharmacovigilance career opportunity.
Key Responsibilities
As a Safety Administrator, you’ll play a vital role in supporting PPD’s pharmacovigilance department by:
- Managing Team Communication: Oversee the team mailbox, ensuring timely responses and efficient communication flow.
- Tracking and Reporting: Maintain accurate records of team- and project-related information, including compliance metrics.
- Supporting Document Preparation: Assist authors by scheduling meetings, drafting planning documents, and preparing data requests.
- Document Compilation: Format and compile final deliverables, ensuring high-quality standards and adherence to deadlines.
- Filing and Organization: Maintain organized records and ensure proper filing of safety-related documents.
- Meeting Deadlines: Work efficiently under strict timelines to meet regulatory and project requirements.
Qualifications and Skills
To succeed in this role, candidates should possess:
- Strong Organizational Skills: Ability to manage multiple tasks and prioritize effectively.
- Attention to Detail: Ensure accuracy in document preparation and data tracking.
- Proficiency in MS Office: Advanced skills in MS Word and Excel for formatting and reporting.
- Typing Proficiency: Fast and accurate keyboard skills for efficient task completion.
- English Language Mastery: Excellent grammar, writing, and communication skills.
- Pharmacovigilance Experience (Preferred): Prior experience in pharmacovigilance or clinical research is a plus.
- Adaptability: Ability to thrive in a fast-paced, evolving environment.
- Teamwork and Independence: Work collaboratively in a remote team while managing tasks independently.
A proactive attitude and the ability to adapt to changing processes are essential for this role.
Benefits of Joining PPD
- Fully Remote Work: Enjoy the flexibility of working from home in India or Philippines.
- Career Growth: Gain experience in pharmacovigilance and clinical research with a global leader.
- Collaborative Environment: Work with a supportive, remote team dedicated to excellence.
- Impactful Work: Contribute to critical safety documents that ensure patient safety and regulatory compliance.
How to Apply
