AstraZeneca Hiring for Central Global Study Associate in Bangalore
AstraZeneca, a global leader in science-led biopharmaceuticals, is inviting applications for the role of Central Global Study Associate (CGSA) in Bangalore, India. This is an excellent opportunity for professionals with 1 to 3 years of experience in clinical research or study operations, especially those with educational backgrounds in B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, or related life science fields.
If you are looking to work in a dynamic, innovation-driven environment with global exposure, this role offers the ideal platform to advance your clinical operations career. AstraZeneca Hiring for Central Global Study Associate
About AstraZeneca
AstraZeneca is a science-focused pharmaceutical company that discovers, develops, and delivers innovative medicines primarily in the therapeutic areas of Oncology, Rare Diseases, and BioPharmaceuticals. The company operates in over 100 countries and is known for its commitment to research, ethical practices, and breakthrough therapies. AstraZeneca Hiring for Central Global Study Associate
AstraZeneca’s culture emphasizes diversity, continuous learning, collaboration, and integrity. The Development Operations Business Enablement team within the company plays a pivotal role in supporting clinical trials across various global locations.
Position Overview
Role: Central Global Study Associate (CGSA) – TMF
Location: Bangalore, India
Experience: 1 to 3 years
Work Type: Full-time (Hybrid model – Minimum 3 days per week onsite)
Industry: Clinical Research and Development
Application Deadline: June 16, 2025
Key Responsibilities
The CGSA will support global clinical study teams across all phases of trials by providing operational and administrative assistance. This includes: AstraZeneca Hiring for Central Global Study Associate
- Executing clinical trial support tasks using a centralized ticketing system (e.g., Investigator Brochure distribution, TMF quality control)
- Managing the setup, maintenance, and closeout of the Trial Master File (TMF), ensuring regulatory and internal compliance
- Coordinating with global study teams to facilitate study initiation, monitoring, and closure activities
- Tracking study timelines and deliverables using specialized systems and tools
- Preparing, reviewing, and formatting study-related documentation with adherence to templates and versioning protocols
- Acting as a subject matter expert (SME) in CGSA-related processes, tools, and best practices
- Supporting internal and external audits, as well as inspection readiness procedures
- Assisting in training and onboarding of new team members
- AstraZeneca Hiring for Central Global Study Associate
Eligibility Criteria
Education
Applicants must hold a degree in one of the following fields:
- B.Pharm or M.Pharm
- Pharm.D
- B.Sc or M.Sc in Life Sciences, Biotechnology, Clinical Research, or related disciplines
Experience
- Minimum 1 year and up to 3 years of experience in clinical research, trial administration, or document management
- Candidates with knowledge of Trial Master File (TMF) processes will be preferred
Required Skills
- Solid understanding of clinical trial execution, regulatory processes, and drug development lifecycle
- Experience with eTMF platforms such as Veeva Systems or equivalent
- Proficiency in Microsoft Office tools (Word, Excel, Outlook, PowerPoint)
- Strong communication skills (verbal and written) in English
- Excellent attention to detail and document handling
- Ability to prioritize tasks, meet deadlines, and work in a high-paced global environment
- Problem-solving aptitude with a proactive approach to cross-functional collaboration
- AstraZeneca Hiring for Central Global Study Associate
Desirable Skills
- Familiarity with ICH-GCP and other regulatory compliance standards
- Exposure to document version control and regulatory correspondence
- Experience in working with global teams or within matrix organizations
- Stakeholder engagement and coordination experience
Benefits of Working with AstraZeneca
- Opportunity to contribute to cutting-edge clinical trials that have global impact
- Work in a highly collaborative environment that fosters innovation and knowledge-sharing
- Structured career growth programs and mentorship
- Flexible working model with a healthy work-life balance
- Inclusive workplace committed to diversity, equity, and continuous professional development
How to Apply
Interested candidates must submit their applications before the closing date. The recruitment process includes initial screening, technical evaluation, and final HR discussion.
Last Date to Apply: June 16, 2025
To apply, visit the official AstraZeneca careers portal or submit your resume through verified job platforms. Ensure that your profile highlights relevant clinical experience and qualifications as listed above. AstraZeneca Hiring for Central Global Study Associate
Final Note
This is an excellent opportunity for professionals seeking to grow in the field of clinical operations while working with one of the world’s most trusted pharmaceutical companies. The Central Global Study Associate role at AstraZeneca offers learning, stability, and international exposure.
Make sure to apply before the application deadline, and prepare your documents for the upcoming screening process. AstraZeneca Hiring for Central Global Study Associate
For more such pharma jobs and clinical research updates, visit Mypharmajob.com regularly.
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