Medical Writer Jobs at OrciMed Life Science – Apply Now

OrciMed Life Science is inviting skilled Medical Writers to join its growing pharmacovigilance and safety writing team. If you have hands-on experience in signal management, aggregate report writing, PSUR/PBRER, PADER, and Risk Management Plans (RMP), this is a strong career opportunity to work with a leading life sciences organization.

Medical writing professionals looking for career growth, stability, and exposure to global regulatory documentation will find this role ideal.

⭐ Key Responsibilities

• Prepare high-quality aggregate safety reports including PSURs, PBRERs, and PADERs
• Perform signal detection and signal management activities
• Draft and update Risk Management Plans (RMPs)
• Work closely with safety physicians, PV teams, and regulatory colleagues
• Ensure compliance with global guidelines (EMA, FDA, ICH, GVP)
• Maintain accuracy, consistency, and data integrity across deliverables
• Contribute to writing templates, quality checks, and process improvement initiatives

🎓 Required Qualifications

• Minimum 3 years of experience in medical writing (pharmacovigilance/safety writing)
• Proven expertise in signal management, PSUR/PBRER, PADER, RMP
• Strong understanding of drug safety regulations and ICH-GVP
• Excellent written and verbal communication skills
• Ability to analyze data and prepare well-structured scientific documents
• Life sciences degree (Pharmacy, Medicine, Biomedical sciences preferred)

🎁 Benefits of Working at OrciMed Life Science

• Competitive salary package (industry-standard for medical writers)
• Exposure to global pharmaceutical safety documentation
• Collaborative and supportive team culture
• Opportunities for career development and continuous learning
• Stable long-term growth in a leading life sciences environment

📩 How to Apply

Eligible candidates can send their updated resume to:
👉 careers@orcimedlifesciences.com

Make sure your subject line reads: Application for Medical Writer – OrciMed