Akkapatri Likitha

Product Manager

Hyderabad, Telangana, India3 yrs experience

Key Highlights

  • Over 3 years of experience in medical information.
  • Expertise in pharmacovigilance and regulatory compliance.
  • Strong analytical skills with a focus on patient safety.
Stackforce AI infers this person is a Healthcare professional specializing in medical information and pharmacovigilance.

Contact

Skills

Core Skills

Medical Information ManagementMedical Inquiry HandlingSafety Database ManagementAdverse Event Reporting

Other Skills

Product Quality Complaints (PQC)Medical & Scientific WritingLiterature & Database ResearchProblem-Solving & Critical ThinkingMedical WritingTeluguCommunicationTeam BuildingCross-functional CollaborationsEnergetic LeadershipClinical AffairsPharmacy EducationCritical ThinkingDatabase SecurityComplaint Management

About

Medical Information Specialist with over 3+ years of experience in delivering accurate, evidence-based scientific and medical information to healthcare professionals, patients, and internal stakeholders. Experienced in handling medical inquiries, adverse event reporting, safety database management, and literature and database research in compliance with global regulatory standards. Skilled in medical and scientific writing, clinical data interpretation, and pharmacovigilance guidelines including US FDA and GVP standards. Known for strong analytical thinking, attention to detail, and effective communication while ensuring regulatory-compliant documentation and high-quality outputs. Adept at working in cross-functional environments and consistently focused on patient safety, compliance, and timely delivery of accurate medical information.

Experience

3 yrs
Total Experience
2 yrs 11 mos
Average Tenure
1 mo
Current Experience

Eversana

Medical Information Specialist

May 2026Present · 1 mo · Pune District, Maharashtra, India · On-site

Mitocon biopharma pvt ltd

2 roles

Medical Information Specialist

Sep 2025Apr 2026 · 7 mos · On-site

  • As a Medical Information Specialist, I support healthcare professionals, patients, and internal teams by delivering accurate, timely, and evidence-based medical and scientific information. My responsibilities include handling medical inquiries, performing literature and database research, and ensuring regulatory-compliant documentation across global standards.
Medical Information ManagementMedical Inquiry Handling

Drug Safety Associate

Apr 2023Aug 2025 · 2 yrs 4 mos · On-site

  • Pharmacovigilance professional with 2.5 years of experience in AE/SAE case processing, Safety database management, Literature research, Regulatory compliance (US FDA/EMA/ICH), Medical & scientific writing, and Clinical data documentation. Strong focus on data accuracy, timelines, collaboration, and patient safety.
Safety Database ManagementAdverse Event Reporting

Education

Vijay College of Pharmacy

Bachelor of Pharmacy - BPharm — Pharmacy

Jan 2018Jan 2022

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