Job Opportunity: Pharmacovigilance and Medical Writing Professionals – OrciMed Life Sciences
Job Summary
OrciMed Life Sciences is pleased to announce a walk-in recruitment drive at our Hyderabad office for experienced professionals in the fields of Pharmacovigilance and Medical Writing. We are looking for skilled individuals to join our growing team as PV Case Processing Specialists and Medical Writers. These roles are ideal for professionals who are adept in ArisG database management, aggregate reporting, and the development of Risk Management Plans (RMP). This is a premier opportunity to contribute to a dynamic life sciences organization while advancing your career in drug safety and regulatory documentation.
Job Responsibilities
1. PV Case Processing Specialist
- Case Management: Execute comprehensive ICSR case processing, including triage, meticulous data entry, and case validation.
- Database Proficiency: Utilize the ArisG safety database for efficient case management and tracking.
- Compliance & Quality: Ensure all activities strictly adhere to global pharmacovigilance regulations. Conduct regular follow-ups and maintain high case quality standards.
- Audit Support: Assist in preparation for audits, regulatory inspections, and reconciliation activities.
2. Medical Writer (Aggregate/RMP)
- Regulatory Documentation: Prepare complex aggregate reports, including PSUR and PBRER, to meet global submission standards.
- RMP Development: Lead the development and ongoing maintenance of Risk Management Plans (RMPs).
- Regulatory Alignment: Ensure all scientific documentation remains compliant with ICH and regional regulatory guidelines.
- Cross-Functional Collaboration: Partner effectively with safety and regulatory teams to ensure accurate and timely delivery of high-quality scientific documents.
Requirements
For PV Case Processing Specialist:
- Experience: A minimum of 2 years of dedicated experience in pharmacovigilance.
- Technical Skills: Mandatory proficiency in the ArisG safety database.
- Knowledge Base: Deep understanding of ICSR workflows, MedDRA coding, and standard safety reporting procedures.
For Medical Writer:
- Experience: A minimum of 1 year of professional experience in medical writing.
- Specialized Skill: Demonstrated experience in creating Aggregate Reports and Risk Management Plans (RMP).
- Regulatory Knowledge: Solid foundation in regulatory writing standards and ICH guidelines.
Core Competencies
Regardless of the specific role, all candidates should possess:
- Strong analytical and scientific writing skills with high attention to detail.
- A thorough understanding of global regulatory frameworks (GVP, ICH).
- A commitment to quality, accuracy, and regulatory compliance.
Benefits of Joining OrciMed
- Global Exposure: Work on projects that span global pharmacovigilance operations.
- Professional Development: Gain hands-on experience in high-level regulatory writing and complex aggregate reporting.
- Career Growth: Advance your expertise within the specialized domains of drug safety and medical communications.
- Work Environment: Join a collaborative, supportive, and rapidly expanding organization within the life sciences sector.
Walk-In Interview Details
We invite interested candidates to attend our walk-in drive to discuss how your expertise aligns with our team’s goals.
- Company: OrciMed Life Sciences
- Location: Union Bank Building, Jubilee Hills, Hyderabad, Telangana – 500033
- Dates: 30th March 2026 – 3rd April 2026
- Time: 10:30 AM to 2:00 PM
How to Apply
To be considered for these roles, please attend the walk-in session in person at the venue specified above.
Please ensure you bring the following:
- Updated Resume: Clearly highlight your specific experience with ArisG, aggregate reporting, and RMP development.
- Identification: A valid government-issued ID proof.
- Documentation: Any relevant educational certificates or proof of previous employment if requested.
We look forward to meeting passionate professionals ready to make a significant impact at OrciMed Life Sciences.