---
title: 'Senior Scientist - Aggregate Reporting at ClinChoice'
canonical: 'https://feeny.ai/job/senior-scientist-aggregate-reporting-clinchoice-bengaluru-j96xdy38vwgn'
type: 'job'
last_seen: '2026-10-28'
---

# Senior Scientist - Aggregate Reporting at ClinChoice

- **Company:** ClinChoice
- **Location:** Bengaluru, India
- **Posted:** 2026-10-28
- **Last confirmed live:** 2026-10-28
- **Apply:** https://job-boards.eu.greenhouse.io/clinchoice/jobs/4955679101

## Job description

Responsibilities:

The Pharmacovigilance Medical Safety Scientist is responsible for developing, reviewing, and maintaining high-quality safety and pharmacovigilance documents that support the safety surveillance and regulatory compliance of consumer health products.

This role requires the ability to synthesize data from multiple sources, including individual case safety reports (ICSRs), aggregate safety data, clinical studies, epidemiological research, literature reviews, post-marketing surveillance, signal detection activities, and other safety data sources. The successful candidate will transform complex safety information into clear, concise, and scientifically accurate documents that support global pharmacovigilance activities and regulatory submissions.

The individual will work closely with Drug Safety, Medical Affairs, Regulatory Affairs, Clinical Development, Quality, and R&D teams to ensure consistent, evidence-based communication of product safety information.

This is an individual contributor role with no direct reports.

Key responsibilities include, but are not limited to:

Pharmacovigilance and Medical Writing:

- Prepare, review, and maintain pharmacovigilance and risk management documents for consumer health products.
- Synthesize safety information from multiple sources, including:
- Individual Case Safety Reports (ICSRs)
- Aggregate safety data analyses
- Clinical trial safety data
- Post-marketing surveillance data
- Epidemiology studies
- Published literature
- Signal detection and evaluation activities
- Benefit-risk assessments
- Health Authority Assessment Reports

Draft and support the preparation of:

- Periodic Safety Update Reports (PSURs/PBRERs/PADERs)
- Ad Hoc Safety Reports
- Development Safety Update Reports (DSURs)
- Signal assessment reports
- Aggregate safety reports
- Risk management documentation
- Health authority responses
- Safety narratives
- Safety sections of regulatory submissions
- Safety surveillance reports and presentations
- Analysis and evaluation for the Safety Management Teams (SMT)

Safety Data Analysis and Interpretation

- Collaborate with Safety Scientists, Medical Reviewers and others to evaluate emerging safety information and communicate findings effectively.
- Assist in the interpretation of safety trends, potential signals, and benefit-risk considerations.
- Support literature surveillance activities and summarize relevant safety findings.
- Contribute to the development of safety conclusions and evidence-based recommendations.
- Support the preparation, review, and analysis of risk management activities and reports.

Quality and Compliance

- Ensure all documents comply with global pharmacovigilance regulations, company SOPs, and applicable guidance documents.
- Maintain high standards of scientific accuracy, consistency, grammar, and document quality.
- Perform quality control reviews of safety documents and ensure timely delivery of assigned projects.
- Support inspection and audit readiness activities through accurate documentation practices.

Education/Experience:

- Advanced degree required: PharmD, PhD, MD, MPH, MS, or equivalent scientific discipline.
- 8-10 years of experience in pharmacovigilance, drug safety, medical writing, regulatory writing, or related pharmaceutical, consumer health, or medical device industries.
- Experience preparing safety and pharmacovigilance documents preferred.
- Familiarity with global pharmacovigilance regulations and safety reporting requirements.
- Experience working in a matrixed environment with multiple stakeholders.

Technical Competencies

- Strong understanding of:
- Clinical research methodologies
- Epidemiology and biostatistics
- Evidence-based medicine
- Regulatory and scientific communication requirements
- Safety and benefit-risk assessment principles

1. Expertise in literature evaluation and scientific data interpretation.
2. Ability to critically analyze multiple complex scientific information and identify key insights to drive product safety.

Skills:

- Excellent medical writing, editing, and proofreading skills.
- Exceptional grammar, attention to detail, and document quality standards.
- Strong analytical and critical thinking capabilities.
- Effective project management and organizational skills.
- Strong verbal and written communication skills.
- Ability to work independently while managing multiple priorities and deadlines.

## About ClinChoice

## Company Overview
- **One-liner**: A global full-service Contract Research Organization (CRO) that accelerates drug and device development for pharmaceutical, biotechnology, medical device, and consumer health companies.
- **Entity Type**: Private (Privately held; Series E funded in 2022)
- **Headquarters**: Horsham, Pennsylvania, United States
- **Founded**: 1995
- **Key Executives**: Ling Zhen (Global Chairman and CEO) [clinchoice.co.jp](https://clinchoice.co.jp/en/about-clinchoice/top-message%E3%83%BBcorporate-philosophy/); John Balian (CEO per LinkedIn) [linkedin.com](https://www.linkedin.com/company/clinchoice)

## Core Business
- **Primary industry**: Pharmaceutical Manufacturing / Clinical Research (Contract Research Organization)
- **Target customers**: B2B – pharmaceutical, biotechnology, medical device, cosmetic, and consumer health companies (enterprise and emerging biopharma)
- **Mission**: “To contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.” [greenhouse.io](https://job-boards.eu.greenhouse.io/clinchoice/jobs/4857865101)

## Products & Services
- **Full-Service Clinical Development**: End-to-end support from pre-clinical through Phase II–IV clinical trials, real-world evidence, and vaccines [clinchoice.com](https://clinchoice.com/about/why-clinchoice/)
- **Functional Service Provider (FSP)**: Dedicated teams for biostatistics, statistical programming, regulatory affairs, medical writing, pharmacovigilance, and data management
- **Strategic Resourcing**: Flexible staffing solutions to supplement client teams with specialized talent
- **Regulatory Affairs & Biometrics**: Services covering CMC, labeling, submissions, and global regulatory strategy
- **Therapeutic Expertise**: Deep capabilities in oncology, cardiovascular, respiratory, immunology, vaccines, infectious diseases, and more

## Market Standing
- **Valuation**: Not publicly disclosed (private company)
- **Key Revenue**: $1.0B (annual) [linkedin.com](https://www.linkedin.com/company/clinchoice)
- **Total Funding**: $212M, including a $150M Series E in July 2022 led by Legend Capital; earlier Series C led by Goldman Sachs [linkedin.com](https://www.linkedin.com/company/clinchoice)
- **Notable Investors/Partners**: Legend Capital, Goldman Sachs; 500+ emerging biopharma partners globally [clinchoice.co.jp](https://clinchoice.co.jp/en/about-clinchoice/top-message%E3%83%BBcorporate-philosophy/)
- **Growth Signals**: 13.2% YoY employee growth (LinkedIn data); acquisition of CROMSOURCE (2023) and CSI Medical Research (2024); expanded to 30+ countries with 4,000+ professionals [linkedin.com](https://www.linkedin.com/company/clinchoice) [clinchoice.com](https://clinchoice.com/about/why-clinchoice/)

## Competitive Advantages
- **30+ years of proven delivery** with over 1,500 full-service clinical studies completed [clinchoice.co.jp](https://clinchoice.co.jp/en/about-clinchoice/top-message%E3%83%BBcorporate-philosophy/)
- **Industry-leading low employee turnover**, ensuring consistent quality and project continuity [clinchoice.com](https://clinchoice.com/about/why-clinchoice/)
- **Full-service and FSP capabilities** across a wide range of therapeutic areas, offering clients seamless end-to-end or modular support
- **Agile, responsive methodology** combined with deep regulatory expertise in major markets (Americas, Europe, Asia-Pacific)
- **Global footprint** (30+ countries) enables efficient multi-regional trials and local knowledge

## Strategic Focus
- Continuing geographic expansion and service innovation through organic growth and strategic acquisitions [clinchoice.co.jp](https://clinchoice.co.jp/en/about-clinchoice/top-message%E3%83%BBcorporate-philosophy/)
- Strengthening capabilities in biotech and emerging biopharma partnerships
- Accelerating commercialization for clients by leveraging global presence and integrated platforms

## Why Work Here
- **Employee-focused culture** with personalized policies and talent development programs [clinchoice.com](https://clinchoice.com/about/why-clinchoice/)
- **Stability and growth**: Low turnover, 13%+ headcount growth YoY, and a 30-year track record
- **Work style**: Hybrid and remote options available; many roles are fully remote (e.g., statistical programmers, biostatisticians) [builtin.com](https://builtin.com/company/clinchoice-1) [greenhouse.io](https://job-boards.eu.greenhouse.io/clinchoice/jobs/4857865101)
- **Global team**: Employees across 30+ countries; diverse team with offices in the US, UK, India, Armenia, Philippines, Colombia, and more
- **Employee ratings**: 3.6/5 overall (245 reviews) – Work-Life Balance 3.6, Culture 3.6, Career 3.5. Compensation rated 2.9/5 [linkedin.com](https://www.linkedin.com/company/clinchoice)
- **Meaningful work**: Contribute to life-saving therapies and devices across oncology, vaccines, and other critical areas

## Sources
1. [clinchoice.com](https://clinchoice.com/about/why-clinchoice/) – “Why ClinChoice?” (official overview, services, culture)
2. [linkedin.com](https://www.linkedin.com/company/clinchoice) – Company page (employees, funding, revenue, acquisitions, reviews)
3. [builtin.com](https://builtin.com/company/clinchoice-1) – Company profile (perks, hybrid/remote policy, careers)
4. [greenhouse.io](https://job-boards.eu.greenhouse.io/clinchoice/jobs/4857865101) – Careers page (mission, current openings)
5. [clinchoice.co.jp](https://clinchoice.co.jp/en/about-clinchoice/top-message%E3%83%BBcorporate-philosophy/) – Corporate philosophy and CEO message (history, values, strategic focus)

## Other roles at ClinChoice

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- [Associate Director, Biostatistics Consultant – Oncology (Remote in Western EU)](https://feeny.ai/job/associate-director-biostatistics-consultant-oncology-remote-in-western-eu-xkmtann6rw7f) — Europe
- [Labeling Operations Manager, Associate Consultant](https://feeny.ai/job/labeling-operations-manager-associate-consultant-clinchoice-colombia-9vn83c22mjy0) — Colombia
- [Labeling Operations Manager, Associate Consultant](https://feeny.ai/job/labeling-operations-manager-associate-consultant-clinchoice-mexico-9gpcnmpcb7qz) — Mexico
- [Global Labeling, Artwork, & U.S. Advertising & Promotion Consultant](https://feeny.ai/job/global-labeling-artwork-u-s-advertising-promotion-consultant-clinchoice-egypt-tvz25rdh0rje) — Egypt
- [Senior Associate, Product Information/Claims Support](https://feeny.ai/job/senior-associate-product-information-claims-support-clinchoice-united-states-rxm65gw1bdb9) — United States
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- [Associate, Regulatory Affairs Consultant](https://feeny.ai/job/associate-regulatory-affairs-consultant-clinchoice-canada-zj0qeb0m2gq7) — Canada
- [Senior Associate - Regulatory Affairs](https://feeny.ai/job/senior-associate-regulatory-affairs-clinchoice-bengaluru-rw25anst49tq) — Bengaluru, India
- [Associate, Medical Writing (MD)](https://feeny.ai/job/associate-medical-writing-md-clinchoice-yerevan-ksn1mxkarzdh) — Yerevan, Armenia