MitoCon BioPharma is a fast-growing pharmaceutical company specializing in drug safety, pharmacovigilance (PV), and clinical research. We are committed to ensuring compliance with global safety regulations while fostering a culture of innovation and excellence

📋 Job Description: Clinical Case Processor

📍 Location: Hyderabad

🕑 Experience Required: 3-6 Years

📌 Job Type: Full-time

🔹 Key Responsibilities:

• Perform case intake, triage, and medical review of adverse event reports.
• Ensure compliance with ICH-GCP, FDA, EMA, and other global regulatory guidelines.
• Use MedDRA and WHO-DD coding for case processing.
• Work with safety databases (Argus, ARISg, etc.) for case submissions.
• Assist in regulatory reporting (CIOMS, PSURs, DSURs, etc.).
• Collaborate with cross-functional teams for timely and accurate case processing.

✅ Eligibility Criteria:

• Bachelor’s/Master’s in Pharmacy, Life Sciences, or related field.
• 3-6 years of hands-on experience in pharmacovigilance case processing.
• Strong knowledge of MedDRA, WHO-DD, and safety databases (Argus/ARISg).
• Excellent communication, documentation, and analytical skills.

💼 Employee Benefits

✔ Competitive salary + performance bonuses
✔ Health insurance & wellness programs
✔ Flexible work environment
✔ Continuous learning & career growth opportunities
✔ Work with a global pharmacovigilance team

📩 How to Apply?

Interested candidates can:

• Send resumes to: hr@mitoconbiopharma.com
• Contact: Keerthi Boga (HR) – +91 9154383165