Suchithra Rachamalla
Linz
Summary
Indian postgraduate student currently pursuing a Master’s in Chemistry and Chemical Technology in Austria, seeking an opportunity in the pharmaceutical or healthcare sector — particularly in pharmacovigilance, regulatory affairs, or quality control. Strong academic foundation in chemistry combined with excellent organizational and analytical skills. Eager to contribute to a forward-thinking organization with a strong vision and mission, while continuing to grow professionally in a multicultural environment.
Overview
11
11
years of professional experience
Work History
Safety science specialist
Fortrea (formerly Labcorp)
04.2023 - 03.2025
- Implemented consistent, efficient and quality processes to meet timelines and deliverables according to requirements and standard operating procedures.
- Ensured compliance of operations with governing regulatory requirements.
- Created, maintained, and assumed accountability for a culture of high customer services.
- Executed drug safety data management processes – a combination of case entry, medical coding, narrative writing, peer review, case follow-up, report preparation and submission to regulatory authorities.
- Performed any other support activities as assigned – tracking various types of information and metrics, ongoing QC of defined process steps, training, reconciliation of data from multiple sources including literature search.
- Assumed responsibility for quality of data processed.
Senior Drug Safety Analyst
Accenture
11.2017 - 10.2022
- Perform data entry, report scheduling in client owned data base like Argus.
- Assist cased report for seriousness, causality, expectedness & validity of safety information and process cases in order to timelines.
- SAE&AE reporting as per regulatory requirement.
- Effective communication with client in contest to any discrepancies raised queries for investigators about any doubt in SAE form also timely follow up for outstanding information.
- Perform quality check for all types of cases.
- Affiliate, (1years, 1month)
- Triage-Initial case creation.
- Follow-up case processing.
- Serious Adverse Event (SAE) and Non-Serious Adverse Event Report Processing for all types of ICSR (Spontaneous NIS and literature).
- Perform the tasks of maintaining the safety database and perform coding of diseases as well as adverse events according to the project-specific coding conventions.
- Assuring medically cohesive narrative with completeness and accuracy.
- Perform follow up letters and questioner to physician / HCP for all type of cases.
- Knowledge sharing sessions, trainings.
- Also has experience working as Line listing QC reviewer and helping the team with seriousness of the cases.
Operation Executive
Hinduja Global Solutions
11.2016 - 08.2017
- Worked as Operation Executive for US Health care helping patients with health Insurances.
Chemist
Sri Krishna Pharmaceuticals
06.2014 - 06.2015
- Worked as Chemist and handled raw materials and WET Analysis.
Education
Masters in Pharmacy - Pharmaceutical Analysis
Jawaharlal Nehru Institute of Technology
05.2016
Masters in Chemistry And Chemical Technology -
Johannes Keppler University
Linz, AustriaSkills
- MS Office
- Pharmacovigilance
- Risk Assessment
- Regulatory Compliance
- Data Analysis
- Adverse Event Reporting
- Knowledge Of Drug Safety Regulations
- Communication Skills
- Project Management
- Quality Assurance
- Team Collaboration
Extra Curricular Activities
Served as "Women's Representative" of Avanti institute of pharmaceutical sciences. Participated & Winner of various cultural & sports activities at college level such as Fashion show, Dance, Drama etc.
Timeline
Safety science specialist
Fortrea (formerly Labcorp)
04.2023 - 03.2025
Senior Drug Safety Analyst
Accenture
11.2017 - 10.2022
Operation Executive
Hinduja Global Solutions
11.2016 - 08.2017
Chemist
Sri Krishna Pharmaceuticals
06.2014 - 06.2015
Masters in Pharmacy - Pharmaceutical Analysis
Jawaharlal Nehru Institute of Technology
Masters in Chemistry And Chemical Technology -
Johannes Keppler University
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