Accenture is actively hiring for multiple Life Sciences R&D roles in India including Clinical Data Services Associate, Clinical eTMF Management (TMF Analyst), and Pharmacovigilance Services Analyst. These roles are ideal for candidates with backgrounds in BSc, Pharmacy, and Life Sciences, looking to build a career in clinical research, clinical data management, and drug safety (PV).
With strong demand for Accenture clinical data jobs in Bangalore and pharmacovigilance analyst jobs in Chennai, this recruitment drive is a high-value opportunity for early and mid-level professionals.
1. Clinical Data Services Associate โ Clinical Data Management (Bangalore)
Location: Bengaluru
Experience: 1โ3 years
Qualification: BSc
Salary: โน3.2 โ โน5.5 LPA (Approx.)
Key Responsibilities:
- Clinical trial data collection, validation, and management
- Ensuring high-quality clinical data for regulatory submissions
- Supporting clinical research and data cleaning activities
- Working with clinical data management systems
- Maintaining compliance with SOPs and regulatory guidelines
Required Skills:
- Strong attention to detail
- Stakeholder management
- Ability to meet deadlines under pressure
- Basic understanding of clinical trials and CDM processes
2. Clinical eTMF Management โ TMF Analyst (Bangalore)
Location: Bengaluru
Experience: 1โ3 years
Qualification: BSc
Salary: โน3.5 โ โน6 LPA (Approx.)
Key Responsibilities:
- Managing Trial Master File (TMF) documentation lifecycle
- Ensuring regulatory compliance of clinical trial documents
- Performing TMF quality checks and reconciliation
- Supporting audit readiness and inspections
- Managing study-level clinical documentation workflows
Required Skills:
- TMF/eTMF knowledge
- Documentation and compliance awareness
- Strong organizational skills
- Ability to manage multiple clinical stakeholders
3. Pharmacovigilance Services Analyst โ Safety Writing (Chennai)
Location: Chennai
Experience: 3โ5 years
Qualification: Graduation (Pharmacy/Life Sciences preferred)
Salary: โน5 โ โน9.5 LPA (Approx.)
Key Responsibilities:
- Writing and reviewing adverse event narratives
- Safety data analysis from clinical trials and post-market surveillance
- Supporting regulatory pharmacovigilance reporting
- Medical literature review and referencing
- Ensuring compliance with global PV guidelines
Required Skills:
- Pharmacovigilance and safety writing experience
- Strong medical documentation skills
- MS Office proficiency
- Experience with Veeva Vault (preferred)
- Good communication and analytical skills
Why Join Accenture Life Sciences?
- Global exposure in clinical research and pharmacovigilance
- Work with leading biopharma clients
- Structured career growth in clinical data and PV domains
- Hybrid and rotational shift opportunities
- Learning in advanced clinical systems and regulatory frameworks
How to Apply?
Application Link For Pharmacovigilance Services Analyst โ Safety Writing (Chennai)
Application Link For Clinical eTMF Management โ TMF Analyst (Bangalore)
Application Link For Clinical Data Services Associate โ Clinical Data Management (Bangalore)
