Micro Data Labs Hiring Scientific and Regulatory Writers (WFH)

Micro Data Labs is expanding its team and is currently hiring for Scientific and Regulatory Writers. This remote job offers a great opportunity to work from anywhere while contributing to high-impact projects in the pharmaceutical and life sciences sectors. If you have at least one year of relevant writing experience, this could be the perfect next step in your career.

Position: Scientific and Regulatory Writers
Job Type: Full-time, Remote (WFH)
Location: Work from Home
Application Deadline: October 5, 2024

Job Overview

As part of the Micro Data Labs writing team, you’ll be responsible for drafting scientific documents, research protocols, manuscripts, and regulatory submissions in line with EU and FDA guidelines. You’ll have the chance to collaborate with teams across different projects, ensuring the delivery of high-quality scientific and regulatory documents. This is an excellent opportunity for candidates who thrive in a remote work environment and want to grow in the scientific writing domain.

1. Scientific Writer Role

Responsibilities:

• Conduct literature searches and review scientific papers to gather relevant data.
• Draft protocols and manuscripts for clinical studies and research projects.
• Write scientific content for journal submissions and other academic platforms.
• Ensure all scientific documents are thoroughly researched, accurate, and formatted according to industry standards.

Qualifications:

• Minimum 1 year of experience as a Scientific Writer.
• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related field.
• Strong ability to search, evaluate, and summarize literature.
• Excellent written communication skills and attention to detail.

2. Regulatory Writer Role

Responsibilities:

• Prepare and draft study protocols, Clinical Study Reports (CSR), and Clinical Evaluation Reports (CER).
• Ensure regulatory documents meet EU and FDA submission guidelines.
• Collaborate with clinical and regulatory teams to ensure accurate and timely submissions.
• Conduct comprehensive reviews and quality control of regulatory submissions before finalization.

Qualifications:

• At least 1 year of experience as a Regulatory Writer.
• Familiarity with FDA and EU regulatory standards and submission processes.
• Bachelor’s or Master’s degree in Pharmacy, Medical Writing, Life Sciences, or a related field.
• Strong understanding of regulatory writing guidelines and formats.

How to Apply

Interested candidates should send their resumes to info@microdatalabs.com. Make sure to highlight your relevant experience in either scientific or regulatory writing. The last date to apply is October 5, 2024.