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Accenture Hiring for Clinical Data (SAS), Regulatory & Pharmacovigilance

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Accenture Careers is actively hiring for multiple Life Sciences and Healthcare roles across India. The company is recruiting experienced candidates for Clinical Data Services, Regulatory Operations, and Pharmacovigilance Safety Writing positions in Mumbai and Bengaluru.

These Accenture jobs are ideal for candidates with B.Pharm, M.Pharm, MSc, and Life Sciences backgrounds looking to build careers in clinical research, regulatory affairs, pharmacovigilance, and drug safety operations.

About Accenture

Accenture Official Website is a global professional services organization specializing in digital, cloud, AI, technology, consulting, and operations. The company operates in more than 120 countries with approximately 791,000 employees worldwide.

Accentureโ€™s Life Sciences R&D division supports pharmaceutical and biotechnology companies in areas including:

  • Clinical Trials
  • Pharmacovigilance
  • Regulatory Affairs
  • Clinical Data Management
  • Drug Safety Operations
  • Medical Writing
  • Patient Services

1. Clinical Data Svs Associate โ€“ Mumbai

Job Overview

DetailsInformation
PositionClinical Data Svs Associate
LocationMumbai
Experience1โ€“3 Years
QualificationBE / MSc / B.Pharm
DepartmentClinical Data Services
SkillSAS Clinical
Job TypeFull Time

Key Responsibilities

  • Manage and process clinical trial data
  • Support clinical data validation and analysis
  • Work on clinical data integration and standardization
  • Ensure data quality and regulatory compliance
  • Collaborate with internal clinical research teams
  • Handle routine operational and reporting tasks

Required Skills

  • Clinical Data Management knowledge
  • SAS Clinical understanding
  • Problem-solving ability
  • Team collaboration skills
  • Quick learning agility
  • Ability to work in rotational shifts

Why This Role Matters

Clinical Data Services professionals help pharmaceutical companies maintain accurate and reliable clinical trial datasets essential for regulatory submissions and drug approvals.


2. LifeScience Regulatory Svs Analyst โ€“ Bengaluru

Job Overview

DetailsInformation
PositionLifeScience Regulatory Svs Analyst
LocationBengaluru
Experience3โ€“5 Years
QualificationB.Pharm / M.Pharm
DepartmentRegulatory Services
DomainRegulatory Operations
Job TypeFull Time

Key Responsibilities

  • Support global regulatory application filings
  • Manage lifecycle submissions including:
    • CMC submissions
    • Amendments
    • Annual reports
    • SPL submissions
  • Process electronic regulatory submissions
  • Coordinate regulatory documentation
  • Ensure compliance with global regulatory requirements

Required Skills

  • Regulatory Affairs experience
  • Stakeholder management
  • Client communication skills
  • Deadline management
  • Adaptability and flexibility
  • Strong documentation handling

Career Scope

This Regulatory Affairs role provides exposure to global regulatory submissions and electronic publishing operations, making it suitable for professionals seeking long-term growth in pharmaceutical regulatory operations.


3. Pharmacovigilance Services Analyst โ€“ Bengaluru

Job Overview

DetailsInformation
PositionPharmacovigilance Services Analyst
LocationBengaluru
Experience3โ€“5 Years
QualificationM.Pharm
DepartmentPharmacovigilance Operations
SkillSafety Writing
Job TypeFull Time

Key Responsibilities

  • Prepare adverse event case narratives
  • Develop safety reports for clinical studies
  • Author and review Risk Management Plans (RMPs)
  • Ensure compliance with SOPs and regulatory guidelines
  • Perform peer quality reviews
  • Support pharmacovigilance documentation activities

Required Skills

  • Pharmacovigilance operations expertise
  • Safety writing experience
  • Risk Management Plan preparation
  • Regulatory compliance understanding
  • Clinical safety documentation knowledge
  • Attention to detail

Why Pharmacovigilance Professionals Should Apply

Accentureโ€™s pharmacovigilance operations team supports global drug safety and risk management activities, providing excellent exposure to international safety reporting standards and regulatory practices.


Benefits of Working at Accenture

Employees at Accenture receive access to:

  • Global work environment
  • Career growth opportunities
  • Learning and development programs
  • Exposure to global pharmaceutical clients
  • Technology-driven healthcare projects
  • Inclusive workplace culture
  • Cross-functional industry experience

How to Apply

Interested candidates can apply directly through the official Accenture Careers portal

Application Link AIOC-S01646101 โ€” Clinical Data Svs Associate

Application Link AIOC-S01646105 โ€” LifeScience Regulatory Svs Analyst

Application Link AIOC-S01646113 โ€” Pharmacovigilance Services Analyst

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