Join Accenture’s Life Sciences Team: Shape the Future of Healthcare!
Summary:
Accenture is seeking motivated and detail-oriented professionals to join our expanding Life Sciences team. We have openings for Clinical Data Services Associates, Life Science Regulatory Services Associates, and Pharmacovigilance Services Associates. These roles offer an excellent opportunity to contribute to cutting-edge projects within the biopharmaceutical industry, working with leading global clients and advanced technologies. If you have a strong academic background in pharmacy, life sciences, or a related field, coupled with relevant experience, we encourage you to apply and take the next step in your career with Accenture.
About Accenture:
Accenture is a global leader in digital, cloud, and life sciences operations, committed to helping our clients transform their businesses and improve the way the world works and lives. We bring innovation, intelligence, and human ingenuity to solve our clients’ most complex challenges. We are proud to foster a diverse and inclusive environment where everyone feels valued and has the opportunity to grow.
We are currently hiring for the following positions:
1. Clinical Data Services Associate – Mumbai
Role Overview:
As a Clinical Data Services Associate, you will play a critical role in managing and validating clinical trial data, ensuring its integrity and adherence to industry standards. You will work closely with clinical data managers, biostatisticians, and other members of the clinical research team.
Key Responsibilities:
- Work on SAS Clinical and CDISC SDTM standards for data management and analysis.
- Validate clinical databases, execute User Acceptance Testing (UAT), and perform edit check testing.
- Identify protocol deviations and conduct CRF/eCRF-based checks to maintain data accuracy.
- Support clinical data management projects and contribute to efficient data integration workflows.
- Adhere to Accenture’s core values and uphold client expectations in all aspects of the work.
Qualifications:
- Bachelor’s degree (BE / B.Pharm) or Master’s degree (MSc) in a relevant field.
- 1-3 years of experience in clinical data management, SAS clinical programming, or CDISC standards.
- Strong analytical, communication, and teamwork skills.
- Ability to work in rotational shifts to support global projects.
2. Life Science Regulatory Services Associate – Bengaluru
Role Overview:
As a Life Science Regulatory Services Associate, you will be responsible for supporting the preparation and submission of regulatory documents to health authorities worldwide. You will play a crucial role in ensuring compliance with global regulatory requirements.
Key Responsibilities:
- Perform eCTD publishing, bookmarking, and hyperlinking activities to create high-quality regulatory submissions.
- Support the preparation of global regulatory submissions, including CMC, Ad-Promo, SPLs, Amendments & LCM documentation.
- Conduct document QC, transform source documents, and verify submission components for accuracy and completeness.
- Coordinate essential regulatory documentation in accordance with ICH guidelines and global regulatory requirements.
Qualifications:
- Bachelor’s degree in Pharmacy (B.Pharm).
- 0-1 year of experience in regulatory publishing, eCTD operations, or document QC.
- Strong attention to detail and adherence to submission standards.
- Availability to work in rotational shifts to support global submissions.
3. Pharmacovigilance Services Associate – Chennai
Role Overview:
As a Pharmacovigilance Services Associate, you will be responsible for managing adverse event reports and ensuring the safety of pharmaceutical products. You will work closely with drug safety physicians and other members of the pharmacovigilance team.
Key Responsibilities:
- Manage the affiliate mailbox and perform reconciliation processes to ensure timely receipt and processing of adverse event reports.
- Handle ICSR case intake, MedDRA coding, processing, submissions, and follow-ups in accordance with global pharmacovigilance regulations.
- Ensure compliance with global PV regulations, client Standard Operating Procedures (SOPs), and internal guidelines.
- Support both serious and non-serious case activities, including data entry, narrative writing, and causality assessment.
Qualifications:
- Bachelor’s degree (B.Pharm) or Master’s degree (M.Pharm) in Pharmacy or a related field.
- 1-3 years of experience in Pharmacovigilance or Drug Safety Database operations.
- Knowledge of MedDRA coding, case processing, and safety regulations.
- Ability to work in rotational shifts to support global operations.
Why Join Accenture?
- Global Impact: Work with leading global pharmaceutical and biotechnology clients.
- Cutting-Edge Technology: Exposure to advanced clinical and regulatory technologies.
- Growth Opportunities: Strong learning culture and clear career progression paths.
- Inclusive Workplace: Inclusive and equal-opportunity workplace that values diversity.
- Diverse Career Paths: Opportunities across clinical research, safety, regulatory & data sciences.
We look forward to receiving your application and exploring how your skills and experience can contribute to our team’s success.