Orcimed Lifesciences is inviting applications for the position of Clinical Trial Case Processing (CTCP) Associate in Hyderabad. This Pharmacovigilance opportunity is ideal for professionals with at least 2 years of experience in Clinical Trial Case Processing and Clinical Trial Safety Submissions. Candidates with hands-on expertise in processing clinical trial safety cases while ensuring compliance with global regulatory requirements are encouraged to apply.

If you are looking to advance your career in Pharmacovigilance, Clinical Trial Safety, Drug Safety, and Clinical Research, this opportunity offers exposure to global safety operations and regulatory compliance.

Job Details

• Position: Clinical Trial Case Processing (CTCP) Associate
• Company: Orcimed Lifesciences
• Department: Pharmacovigilance
• Location: Hyderabad, Telangana
• Experience Required: Minimum 2 Years
• Employment Type: Full-Time

Key Responsibilities

• Process and manage Clinical Trial Case Processing (CTCP) activities.
• Review and evaluate clinical trial safety cases accurately.
• Perform Clinical Trial Safety submissions within regulatory timelines.
• Ensure compliance with global pharmacovigilance regulations and SOPs.
• Maintain high-quality safety documentation and case processing standards.
• Collaborate with cross-functional clinical and drug safety teams.
• Support regulatory inspections and quality audits when required.
• Ensure timely reporting of adverse events and clinical trial safety information.

Required Qualifications

• Bachelor’s or Master’s degree in B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, Microbiology, Biochemistry, Nursing, or other related Life Science disciplines.
• Minimum 2 years of Pharmacovigilance experience.
• Hands-on experience in Clinical Trial Case Processing (CTCP).
• Experience in Clinical Trial Safety Submission.
• Strong understanding of global Pharmacovigilance regulations and ICH-GCP guidelines.
• Excellent communication and documentation skills.

Preferred Skills

• Clinical Trial Case Processing
• Pharmacovigilance Operations
• Clinical Trial Safety Submission
• Drug Safety
• Adverse Event Processing
• Global Regulatory Compliance
• ICH-GCP Guidelines
• Case Processing Workflow
• Safety Database Experience
• Quality Compliance

Why Join Orcimed Lifesciences?

• Opportunity to work on global clinical trial safety projects.
• Exposure to international pharmacovigilance standards.
• Career growth in Clinical Trial Safety and Drug Safety Operations.
• Collaborative and professional work environment.
• Excellent learning opportunities within Pharmacovigilance.

Salary

Based on current Hyderabad Pharmacovigilance market trends for professionals with 2+ years of experience:

Expected Salary: ₹5.8 LPA – ₹8.5 LPA (Estimated)

Actual compensation will depend on experience, technical expertise, and interview performance.

How to Apply

Interested candidates can share their updated resume to:

Email: careers@orcimedlifesciences.com

Apply as early as possible since positions may be filled on a rolling basis.