Hiring for Study Monitor Support Specialist at AstraZeneca
AstraZeneca, a globally recognized pharmaceutical company known for its research-driven innovations, is currently hiring for the position of Study Monitor Support Specialist in Bangalore. This role offers a unique opportunity to support the Regulatory Toxicology and Safety Pharmacology team in managing non-clinical studies. If you have a background in pharmacology, toxicology, or a related field and are looking for a dynamic role in drug safety and regulatory research, this position may be ideal for you. Hiring for Study Monitor Support Specialist
Job Overview
- Position: Study Monitor Support Specialist
- Company: AstraZeneca
- Location: Bangalore, India
- Experience Required: 1–3 Years
- Education: Bachelor’s or Master’s degree in Pharmacology, Toxicology, or a related discipline
- Work Mode: Hybrid (Minimum 3 days/week onsite)
- Last Date to Apply: June 14, 2025
- Application Mode: Online
About AstraZeneca
AstraZeneca is a science-led biopharmaceutical company operating in over 100 countries. With a strong focus on oncology, cardiovascular, respiratory, and immunology, the company is committed to transforming patient outcomes through innovative science and technology. The Bangalore site is a strategic global hub for many of AstraZeneca’s core functions, including R&D and regulatory operations. Hiring for Study Monitor Support Specialist
Role Summary
The Study Monitor Support Specialist will play a critical role in supporting non-clinical toxicology and pharmacology studies, particularly in GLP (Good Laboratory Practice) settings. The role is designed to assist study monitors in managing study workflows, financials, documentation, and quality control.
This position is not lab-based but supports critical back-end operations for drug safety studies that ensure regulatory compliance and data integrity before clinical trials begin. Hiring for Study Monitor Support Specialist
Key Responsibilities
The selected candidate will:
- Support non-clinical study monitors in day-to-day project and study tasks.
- Maintain and update study-related documents to ensure compliance with regulatory standards.
- Assist in the financial management of studies, including:
- Approving invoices
- Creating and managing purchase orders
- Tracking study budgets
- Conduct quality checks (QC) on submission documents to ensure data accuracy and regulatory alignment.
- Analyze and report study metrics for internal evaluations and decision-making.
- Coordinate with global cross-functional teams to ensure the timely and smooth execution of toxicology studies.
- Suggest and implement process improvements to enhance operational efficiency and streamline documentation workflows.
- Hiring for Study Monitor Support Specialist
Required Qualifications & Skills
Educational Background:
- Bachelor’s or Master’s degree in:
- Pharmacology
- Toxicology
- Biomedical Sciences
- Or any related life science field
Essential Skills:
- Proficiency in Microsoft Office tools, especially Excel, Word, and PowerPoint
- Strong verbal and written communication skills in English
- Experience working in or supporting a GLP-certified toxicology lab (preferred)
- Excellent organizational and multitasking capabilities
- Exposure to project coordination or study documentation
- Ability to interact with global stakeholders and teams in a professional manner
Preferred Experience:
- Familiarity with CRO (Contract Research Organization) operations and study management
- Experience working in multidisciplinary teams across geographies
- Demonstrated capability in process optimization and efficiency tracking
- Hiring for Study Monitor Support Specialist
Why Choose AstraZeneca?
1. Research-Driven Culture
AstraZeneca is known for its unwavering commitment to innovation. You will be contributing to studies that support new drug development and regulatory approval.
2. Global Exposure
As part of the Bangalore hub, you will collaborate with experts from across the world, gaining insights into international regulatory frameworks and study protocols.
3. Career Development
AstraZeneca invests in employee development through regular training, mentorship programs, and opportunities for vertical and cross-functional growth.
4. Inclusive Environment
The company promotes diversity, equity, and inclusion, ensuring a respectful and empowering work environment for all.
5. Hybrid Work Model
The position offers the flexibility of working from home with a requirement to be present in the office for at least 3 days a week, ensuring work-life balance.
Who Should Apply?
This position is ideal for: Hiring for Study Monitor Support Specialist
- Candidates looking to transition from lab work to regulatory operations
- Professionals with toxicology or pharmacology degrees who want to enter global study support roles
- Individuals aiming to build a career in regulatory documentation and non-clinical project management
- Those interested in pharmaceutical R&D without direct benchwork involvement
How to Apply?
Interested applicants should apply directly through the official AstraZeneca careers page or through trusted pharmaceutical job platforms like Pharmabharat, which provides verified listings and real-time job alerts. Hiring for Study Monitor Support Specialist
Make sure to prepare the following:
- An updated resume highlighting experience in toxicology, study monitoring, or GLP environments
- A brief cover letter emphasizing your understanding of non-clinical study processes and your motivation for joining AstraZeneca
Final Words
If you are passionate about drug safety, data integrity, and regulatory processes in preclinical research, this role at AstraZeneca can offer you both challenge and career advancement. The position is time-sensitive, so ensure you apply before the closing date on June 14, 2025. Hiring for Study Monitor Support Specialist
Begin your journey with one of the world’s most respected pharmaceutical companies and be a part of innovations that shape the future of medicine.
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