Senior Medical Writer & Submission Lead

Parexel; Singapore; On-site; SGD 120,000 - 180,000; Full time

Job summary

Parexel is a global biopharma partner focused on improving health by advancing clinical development. The team emphasizes empathy, collaboration, and accountability to deliver high-quality medical writing and regulatory documents.

The role involves leading writers, coordinating submissions, maintaining client relationships, and driving project success in a fast-paced environment. Strong communication, leadership, and clinical writing expertise are essential.

Qualifications

• Broad understanding of clinical research and drug development process.
• Experience in preparing clinical regulatory documentation.

Responsibilities

• Author Clinical Documents for regulatory submission with minimal supervision.
• Lead writer/submission coordinator and client contact to manage multiple writers.
• Provide leadership and strategic planning to ensure timely, on-budget project delivery.
• Coordinate work plans and monitor progress across documents and teams.
• Maintain client relationships and disseminate project information across teams.

Skills

Interpersonal communication

Negotiation

Verbal communication

Written communication

Multitasking

Team leadership

Education

Bachelor's degree in Life Sciences/Health Related Sciences

Tools

MS Word

SharePoint

Excel

File conversion

Job description

Parexel is a global biopharma partner focused on improving health by advancing clinical development. The team emphasizes empathy, collaboration, and accountability to deliver high-quality medical writing and regulatory documents.

The role involves leading writers, coordinating submissions, maintaining client relationships, and driving project success in a fast-paced environment. Strong communication, leadership, and clinical writing expertise are essential.