Job Title: Clinical Data Services Senior Analyst
Skill Required: Clinical Data Services – SDTM Mapping
Qualification: MSc
Experience: 5–8 years
Location: Bengaluru

About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. Combining unmatched experience and specialized skills across more than 40 industries, we provide Strategy & Consulting, Technology, and Operations services, and Accenture Song—powered by the world’s largest network of Advanced Technology and Intelligent Operations centers.
Our 699,000 employees deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners, and communities.

What Would You Do?

You will be aligned with the Life Sciences R&D vertical. Our services span the entire life sciences enterprise—including research laboratories, clinical trial support, regulatory services, pharmacovigilance, and patient service solutions.

You will work within the Clinical, Pharmacovigilance & Regulatory sub-offering, helping leading biopharma companies bring their vision to life by improving outcomes, converging around the patient, and connecting scientific expertise with deep patient insights.

You will be part of the Clinical Data Management team responsible for:

• Collection, integration, and delivery of clinical data with the highest quality and cost efficiency

• Discrepancy review, query generation, and query resolution

• Creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines

• Identifying and raising protocol deviations

• Edit check validation, test case creation, test script writing, and database validation (UAT)

• Managing clinical data management projects

• Supporting standardized structures for human clinical trial and nonclinical study data (SDTM) for FDA and other regulatory submissions

What Are We Looking For?

• Adaptable and flexible

• Ability to perform under pressure

• Strong problem-solving skills

• Excellent attention to detail

• Ability to establish strong client relationships

Roles and Responsibilities

• Bachelor’s degree in Life Sciences or equivalent (mandatory)

• For programming roles: bachelor’s degree in Computer Science, IT, or related discipline

• Expertise in:

  • Clinical data harmonization

  • CDISC standards (SDTM, ADaM)

  • Evaluation and manipulation of pooled clinical datasets (preferred)

• PG Diploma in Clinical Research & Trial Management (added advantage)

• Therapeutic area knowledge preferred:

  • Cardiovascular

  • Neuroscience

  • Oncology (solid tumors)

• Strong verbal and written communication skills

• Strong interpersonal skills and ability to collaborate across functions

• Proficiency in Microsoft Excel, Word, and PowerPoint

• Knowledge of ICH, GCP, and relevant regulatory guidelines for clinical documentation

• Ability to work in a fast-paced environment with shifting priorities

• High attention to detail and accuracy