Accenture Fresher Recruitment | Clinical Data Associate
- B.Pharm/BE Clinical Data Associate Opening Bengaluru
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Work Style & Expectations
- Eligibility / Qualifications
- Required Education
- Relevant Courses (comma-separated)
- Experience
- Skill Requirements
- Location & Salary
- Application Process
- FAQs
- Is this role suitable for freshers?
- What background is preferred?
- Will I need to work in shifts?
- Are clinical data management skills required?
- Does the role involve coding?
- Summary Table
B.Pharm/BE Clinical Data Associate Opening Bengaluru
Accenture hiring BE/B.Pharm/M.Pharm candidates for Clinical Data Services Associate roles in Bengaluru. 0–3 years experience.
Accenture is hiring Clinical Data Services Associates in Bengaluru for its Life Sciences R&D vertical. This role suits science and pharmacy graduates who want to build a career in clinical data management, medical monitoring, and clinical operations. If you are looking for a structured opportunity in a global organization where you can grow your clinical research skills, this position offers the right platform.
Company Overview
Accenture is a leading global professional services organization delivering digital, cloud, and consulting solutions across 120+ countries. With deep expertise in Life Sciences R&D, Accenture supports biopharma companies with clinical trial operations, pharmacovigilance, regulatory services, and patient-focused solutions. The Life Sciences practice integrates scientific knowledge with data-driven technologies to improve trial quality and patient outcomes.
Job Role & Responsibilities
The Clinical Data Services Associate will support clinical data management and medical monitoring activities across global clinical trials.
Key Responsibilities
- Perform discrepancy review, query generation, and query resolution in clinical databases
- Create and maintain CRF Completion Guidelines (CCG)
- Review and reconcile Serious Adverse Events (SAE) data
- Identify protocol deviations and raise appropriate documentation
- Develop and validate edit checks; write test cases and test scripts
- Support User Acceptance Testing (UAT) for clinical trial databases
- Assist with medical monitoring tasks, review protocol requirement specifications, and ensure accuracy against SOPs
- Collaborate with internal teams to support data quality and trial oversight
Work Style & Expectations
- Solve routine problems using established guidelines and SOPs
- Work as an individual contributor within a detailed, instruction-oriented framework
- Interact mainly with your team and supervisor
- Be flexible for rotational shifts as required
Eligibility / Qualifications
Required Education
- BE (Engineering)
- Bachelor of Pharmacy (B.Pharm)
- Master of Pharmacy (M.Pharm)
Relevant Courses (comma-separated)
B.Pharm, M.Pharm, BE Biotechnology, BE Biomedical, Clinical Research Certification, Clinical Data Management Course, PG Diploma in Clinical Trials.
Experience
- 0 to 3 years in clinical research or data management
- Freshers with strong analytical and communication skills may also apply
Skill Requirements
- Strong analytical ability
- Good written and verbal communication
- Flexibility and adaptability
- Understanding of clinical trial processes (preferred)
Location & Salary
- Location: Bengaluru, Karnataka
- Work Model: Full-time; rotational shifts as needed
- Salary: Competitive compensation based on experience and qualifications
Application Process
Click the link below to apply directly through Accenture’s career portal:
Apply Here: https://www.accenture.com/in-en/careers/jobdetails?id=AIOC-S01614645_en&title=Clinical+Data+Svs+Associate
Prepare your resume to highlight:
- Clinical data or research exposure
- Technical or analytical coursework
- Any internship or project work related to life sciences
FAQs
Is this role suitable for freshers?
Yes. Candidates with 0–3 years of experience can apply.
What background is preferred?
Pharmacy graduates, BE holders, and candidates with clinical research exposure.
Will I need to work in shifts?
Yes. The role may require rotational shifts.
Are clinical data management skills required?
Preferred but not mandatory; training and structured guidance will be provided.
Does the role involve coding?
No coding is required. The focus is on clinical data review, validation, and monitoring.
Summary Table
| Category | Details |
|---|---|
| Company | Accenture, Bengaluru |
| Vacancies | Clinical Data Services Associate |
| Required Education | BE, B.Pharm, M.Pharm |
| Experience | 0–3 years (clinical data or CR experience preferred) |
To apply for this job please visit www.accenture.com.
