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Are you a passionate medical writer with hands-on experience in pharmacovigilance and Risk Management Plans (RMPs)?
Apcer Lifesciences — a global leader in life sciences and safety services — is looking for an experienced Senior Safety Medical Writer to join its growing team.
This role offers an incredible opportunity to contribute to drug safety documentation, regulatory compliance, and global pharmacovigilance excellence.
🩺 Key Responsibilities
As a Senior Safety Medical Writer, you will:
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- Author and review Risk Management Plans (RMPs) in accordance with EMA and global regulatory guidelines.
- Prepare and update aggregate safety reports (PSURs, PBRERs, DSURs).
- Collaborate with cross-functional teams in pharmacovigilance, regulatory affairs, and medical affairs.
- Ensure scientific accuracy, clarity, and consistency in safety documents.
- Participate in quality review and training initiatives related to safety writing.
- Maintain compliance with GVP, ICH, and company SOPs.
🎓 Qualifications & Experience
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Medicine, or related field.
- Minimum 3–4 years of experience in pharmacovigilance / safety medical writing.
- Strong understanding of Risk Management Plans (RMPs) and safety regulations.
- Excellent written and verbal communication skills.
- Ability to work effectively in a cross-functional, global team environment.
💼 Why Join Apcer Lifesciences?
- Opportunity to work with a global pharmacovigilance leader.
- Exposure to international safety documentation standards.
- Supportive work culture promoting learning and growth.
- Competitive salary package and hybrid work flexibility.
📝 How to Apply
If you meet the above criteria and are ready to advance your career in safety medical writing, send your updated resume to:
📧 tanya.saini@apcerls.com
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