🛠 Tech Stack

💼 About This Role

You'll execute data screening and collection for systematic literature reviews supporting medical device regulatory documents. Your work directly impacts Clinical Evaluation Reports and Post-Market Surveillance activities. Join a global CRO with a collaborative one-team culture.

🎯 What You'll Do

• Screen and collect data from literature using software tools like Excel.
• Comply with client metrics and project timelines.
• Collaborate with Medical Writers and other specialists for quality.
• Escalate project risks or issues to senior members.

📋 Requirements

• Bachelor's degree in life sciences.
• 1-5 years experience in medical writing or related field.
• Proficiency in Microsoft Office Suite.
• Excellent English communication skills.

✨ Nice to Have

• Experience in systematic literature reviews.
• Knowledge of regulatory documents (CER, SSCP, PSUR).

🎁 Benefits & Perks

• ⏰ Flexible Working Hours
• 📈 Full performance and development process
• 🎉 Team events and end of year party
• 🏥 Health Insurance

📨 Hiring Process

Estimated timeline: 1-2 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2Interview· 60 min