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Kyla Jamotillo

@kylajamotillo

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Pharmacovigilance Submission Associate at Celltrion Inc., coordinating ICSR submissions to regulatory authorities.

Philippines

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At Celltrion Inc., I coordinate and execute timely submissions of Individual Case Safety Reports (ICSRs) for partner distribution and regulatory authorities. I review data accuracy and reporting guidelines to support the quality and compliance of safety submissions.

Previously at Celltrion Inc., I processed pharmacovigilance data in Argus Safety, assessed case validity, and evaluated event seriousness, listedness, and causality. I also drafted case narratives, comments, and query letters according to Standard Operating Procedures.

At Publicis Groupe, I supported media teams with data analysis and reporting, transforming raw data into competitive reports using Power Query and Excel. Earlier, at Zuellig Pharma, I supported secondary repackaging operations, including generating work instructions and reviewing batch records.

Experience

Work history, roles, and key accomplishments

Current

Pharmacovigilance Submission Associate

Current

Celltrion Inc

Jul 2025 - Present (1 year 4 months)

Coordinate and execute timely submission of Individual Case Safety Reports (ICSRs) for partner distribution and per Regulatory Authority guideline for submission to regulatory authorities.

• Maintain knowledge of global pharmacovigilance (PV) regulatory requirements, including FDA, EMA, MHRA and Health Canada.
• Utilize regulatory submission platform and tools such as ICSR Gateway and MHRA websi

Pharmacovigilance Data Entry Associate

Celltrion Inc

Oct 2024 - Jul 2025 (9 months)

Ensure the safety and efficacy of biosimilar products through monitoring, assessing, and reporting of adverse events to safeguard the public health while adhering to international regulatory standards.

• Receive initial/follow-up reports and assess its validity (reporter, patient identifiers, adverse events, drug).
• Perform data entry of patient information using Argus Safety database while ensu

Integrated Data Specialist

Publicis Groupe

Jul 2023 - Sep 2024 (1 year 2 months)

Support the day-to-day integrated data, reporting and analytics requirements of the client media teams for their media strategy and plan requirements.

• Utilize analysis software tools such as Nielsen Arianna, Kantar Radio analytics, Digital Ad Intel, and eRAM needed for the media plan and strategy.
• Transform raw data into a granular competitive report through Power Query, Pivot table and basi

Secondary Repackaging Associate

Zuellig Pharma

Apr 2022 - Jul 2023 (1 year 3 months)

Liaise with key persons from pharmaceutical companies regarding their secondary repackaging request and responsible for overseeing the conversion from raw materials to finished good products.

• Generate Repackaging Work Instructions (RWI) for a specific production order.
• Conduct training for Zuellig's third party personnel on SOP relevant to day-to-day repackaging operations.
• Provide additi