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Accenture Hiring for Clinical Data Management Medical Monitoring

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Accenture is hiring for the role of Clinical Data Services Associate in Bengaluru. Candidates with B.Pharm, M.Pharm, or BE qualifications and 1-3 years of experience in clinical data management, pharmacovigilance, or life sciences domains are eligible to apply.

This is an excellent opportunity for pharmacy and life sciences professionals looking to build a career in Clinical Data Management, Medical Monitoring, and Clinical Research Operations with one of the worldโ€™s leading healthcare consulting companies.


Job Overview

DetailsInformation
Job RoleClinical Data Services Associate
CompanyAccenture
LocationBengaluru
Experience1-3 Years
QualificationB.Pharm, M.Pharm, BE
DepartmentClinical Data Services โ€“ Medical Monitoring
Job TypeFull Time
ShiftRotational Shifts
Job IDAIOC-S01647299

About Accenture

Accenture Careers is a global professional services company specializing in digital transformation, cloud computing, AI, operations, and healthcare solutions. With operations in more than 120 countries and over 790,000 employees worldwide, Accenture supports pharmaceutical and biotechnology companies through clinical research, pharmacovigilance, regulatory affairs, and patient safety services.

The companyโ€™s Life Sciences R&D division focuses on accelerating drug development and improving patient outcomes using advanced clinical and data-driven solutions.


Clinical Data Services Associate Job Description

As a Clinical Data Services Associate, candidates will work within Accentureโ€™s Life Sciences R&D vertical supporting clinical trial data management and medical monitoring activities.

The role involves managing and validating clinical trial data, ensuring protocol compliance, and supporting safety monitoring activities during clinical studies.

Professionals in this role will collaborate with internal teams and supervisors to ensure high-quality clinical data management aligned with SOPs and regulatory standards.


Key Responsibilities

  • Support clinical data collection, validation, and processing activities
  • Review protocol requirement specifications and clinical documentation
  • Assist in medical monitoring and clinical safety oversight
  • Ensure compliance with SOPs and regulatory guidelines
  • Resolve routine clinical data issues using established procedures
  • Work collaboratively with team members and supervisors
  • Maintain accurate clinical trial records and documentation
  • Participate in rotational shifts based on project requirements

Required Skills

Candidates applying for the Accenture Clinical Data Services Associate role should possess:

  • Strong written and verbal communication skills
  • Problem-solving and analytical abilities
  • Adaptability and flexibility in dynamic work environments
  • Basic understanding of clinical trials and clinical data management
  • Knowledge of medical monitoring and pharmacovigilance concepts
  • Ability to follow SOPs and quality standards

Eligibility Criteria

Educational Qualification

  • Bachelor of Pharmacy (B.Pharm)
  • Master of Pharmacy (M.Pharm)
  • BE graduates

Experience

  • 1 to 3 years of relevant experience in:
    • Clinical Data Management
    • Clinical Research
    • Pharmacovigilance
    • Medical Monitoring
    • Healthcare Operations
  • Freshers Can Apply Too | Ask For Reference from Accenture employees

Salary and Benefits

The estimated salary for the Clinical Data Services Associate role at Accenture ranges between โ‚น4.5 LPA โ€“ โ‚น7.2 LPA, depending on experience, project expertise, and interview performance.

Employee Benefits

  • Global healthcare projects exposure
  • Career growth opportunities in Clinical Research and Pharmacovigilance
  • Training and development programs
  • Diverse and inclusive work culture
  • Work with leading biopharma clients
  • Health and wellness benefits

Why Join Accenture?

Working at Accenture offers strong exposure to clinical operations, clinical trial support, and healthcare technology projects. Candidates interested in long-term careers in Clinical Data Management and Life Sciences Operations can gain valuable industry experience and global project exposure.

This role is especially suitable for professionals aiming to transition into:

  • Clinical Research Associate (CRA)
  • Clinical Data Analyst
  • Pharmacovigilance Specialist
  • Drug Safety Associate
  • Regulatory Operations roles

How to Apply

Application Link

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