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Clinical Data Svs Specialist

Accenture
Accenture
7-11 years
preferred by company
10 Jan. 26, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Services Specialist / Team Lead – Clinical Reports Management

Job ID: AIOC-S01619734
Employment Type: Full-Time
Experience Required: 7–11 Years
Location: Bengaluru, India
Function: Clinical Data Services / Life Sciences R&D
Industry: Pharmaceuticals, Biotechnology, Clinical Research

Job Overview

Accenture is seeking an experienced Clinical Data Services Specialist / Team Lead to join its Life Sciences R&D practice in Bengaluru. This senior-level role focuses on clinical data services and clinical reports management, supporting global biopharmaceutical clients in delivering high-quality, regulatory-compliant clinical trial data.

The position plays a key role in managing clinical data reporting, database programming, and analytics across complex clinical trials, enabling accurate evaluation of safety and efficacy outcomes.

Key Responsibilities

As a Clinical Data Services Specialist, you will contribute to and lead clinical data reporting initiatives across multiple studies while ensuring adherence to global regulatory and quality standards.

Primary Responsibilities Include:

  • Develop and deliver clinical trial reports in accordance with study requirements and regulatory guidelines

  • Create reports using SAS, J-Review, Cognos, SQL, and PL/SQL

  • Support clinical data services including data collection, validation, processing, storage, and analysis

  • Design, build, and support Clinical EDC systems and database programming activities

  • Ensure data accuracy, consistency, and inspection readiness across clinical trials

  • Analyze and solve moderately complex clinical data and reporting challenges

  • Adapt existing methodologies or develop new solutions where required

  • Understand and align deliverables with strategic objectives set by senior leadership

  • Collaborate with internal teams, supervisors, and client stakeholders

  • Manage small teams or workstreams and provide technical guidance as needed

  • Support business requirements that may include rotational shift schedules

Education & Experience Requirements

  • Bachelor’s degree in Engineering (BE/BTech) or equivalent technical qualification

  • 7 to 11 years of relevant experience in clinical data services, clinical reporting, or life sciences analytics

  • Strong hands-on experience in clinical database programming and reporting tools

Required Skills & Technical Expertise

  • Clinical Database Programming

  • Clinical EDC Build and Design

  • Clinical Reports Management

  • Strong proficiency in SAS, J-Review, Cognos, SQL, and PL/SQL

  • Solid understanding of clinical trial processes and life sciences R&D workflows

  • Ability to manage complex datasets and ensure regulatory compliance

  • Strong analytical, problem-solving, and decision-making skills

  • Effective communication and stakeholder management capabilities

Role Characteristics

  • Senior individual contributor or team lead role

  • Decisions may significantly impact project delivery and team outcomes

  • Interaction with peers, supervisors, and client stakeholders

  • Guidance provided for new or complex assignments

  • May involve managing small teams or defined project efforts

  • Role may require working in rotational shifts

About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud, and security. With approximately 699,000 professionals across more than 120 countries, Accenture delivers strategy, consulting, technology, and operations services across over 40 industries.

Accenture’s Life Sciences R&D practice supports the full clinical development lifecycle, including clinical operations, data management, pharmacovigilance, regulatory services, and patient-centric solutions—helping global biopharmaceutical organizations improve outcomes and accelerate innovation.

Why Join Accenture

  • Work with leading global biopharma and life sciences organizations

  • Engage in high-impact clinical trials and regulatory-driven data initiatives

  • Advance your career in clinical data services and life sciences analytics

  • Access continuous learning, leadership development, and global exposure

  • Be part of a collaborative, innovation-driven, and inclusive work environment