Clinical Research Associate | AstraZeneca Delhi | Life Sciences Graduate

Clinical Research Associate | AstraZeneca Delhi | Life Sciences Graduate

Apply for Clinical Research Associate at AstraZeneca, Delhi. Life Sciences graduates with CRA experience preferred. Apply before 14 Nov 2025.

---

Be part of a global team that’s transforming the future of medicine. AstraZeneca, a world leader in biopharmaceutical innovation, is hiring for the position of Clinical Research Associate (CRA) in New Delhi, India. This role offers a unique opportunity to work on groundbreaking research studies, ensuring the ethical and efficient conduct of clinical trials that improve patient outcomes globally.

If you’re passionate about clinical operations, GCP compliance, and data quality, this role will place you at the heart of life-changing research.

---

Company Overview

AstraZeneca is a science-led, patient-focused global biopharmaceutical company headquartered in Cambridge, UK. Operating in over 100 countries, AstraZeneca is dedicated to discovering, developing, and commercializing prescription medicines in oncology, cardiovascular, renal, respiratory, and rare disease areas.

With an inclusive and innovation-driven culture, AstraZeneca fosters collaboration across diverse teams to bring next-generation therapies to life. The company’s India operations play a pivotal role in advancing clinical trials, pharmacovigilance, and regulatory excellence.

AstraZeneca has been recognized globally as a Great Place to Work, emphasizing integrity, diversity, and scientific excellence in all aspects of research and operations.

---

Job Role & Responsibilities

As a Clinical Research Associate (CRA), you will play a vital role in supporting the planning, execution, and monitoring of clinical studies in compliance with ICH-GCP guidelines and AstraZeneca’s SOPs.

Key Responsibilities:

• Participate in investigator selection and site qualification visits.
• Manage regulatory and ethics submissions, ensuring accurate documentation for EC/IRB and authorities.
• Conduct site initiation, monitoring, and close-out visits as per the study Monitoring Plan.
• Ensure all investigators and site staff complete ICH-GCP and protocol-specific training before and during the study.
• Maintain inspection readiness by adhering to documentation and compliance standards.
• Drive site performance by monitoring patient recruitment and protocol adherence.
• Ensure timely data entry, query resolution, and eTMF updates.
• Perform Source Data Verification (SDV) and Source Data Review (SDR) to ensure data quality.
• Manage study supplies, including Investigational Site Files (ISF) and drug accountability.
• Support SAE reporting and ensure prompt follow-up with sites.
• Participate in audit and inspection preparation, ensuring compliance with regulatory requirements.
• Collaborate with cross-functional teams and contribute to Local Study Team (LST) meetings.
• Escalate quality or GCP compliance issues promptly and support resolution efforts.

---

Eligibility / Qualifications

Educational Background:

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or related fields.

Experience Requirements:

• 2–5 years of experience as a Clinical Research Associate or Clinical Trial Monitor within a CRO, sponsor, or pharmaceutical environment.

Core Competencies:

• Strong knowledge of ICH-GCP, local regulations, and clinical trial operations.
• Excellent communication and interpersonal skills.
• Proficiency in CTMS, eTMF, and data management systems.
• Detail-oriented with a focus on quality and compliance.
• Ability to multitask and work independently with cross-functional teams.

Preferred Skills:

• Experience with Risk-Based Quality Management (RbQM).
• Familiarity with regulatory submission processes and site start-up activities.
• Knowledge of drug accountability and investigational product handling.

---

Location & Salary

• Location: New Delhi, India
• Department: Clinical Operations / Research
• Experience Level: 2–5 years
• Work Type: Full-Time, On-site
• Compensation: Competitive salary based on experience with performance-based incentives.
• Job ID: R-238617
• Application Deadline: 14 November 2025

---

Application Process

Interested candidates can apply directly through AstraZeneca’s official careers portal. Ensure your resume highlights clinical trial experience, regulatory understanding, and familiarity with GCP compliance.

👉 Apply Here – AstraZeneca Careers Portal

⚠️ Apply before 14 November 2025 to secure your place in one of the world’s most trusted names in clinical research.

---

Why Join AstraZeneca?

• Work with a global leader in biopharmaceutical innovation.
• Opportunity to contribute to cutting-edge clinical research and medical advancements.
• Access to continuous professional development and leadership programs.
• Inclusive work environment focused on diversity, learning, and empowerment.
• Be part of a company that values integrity, science, and collaboration in improving global healthcare outcomes.

---

FAQs

Q1: What qualifications are needed for the CRA role at AstraZeneca?
A degree in Life Sciences, Pharmacy, Nursing, or related fields is required.

Q2: How many years of experience are required?
Applicants should have 2–5 years of experience in clinical research or trial monitoring.

Q3: What is the location and work mode?
The role is based in New Delhi, India, with on-site responsibilities.

Q4: What kind of trials does AstraZeneca conduct?
The company focuses on trials in oncology, cardiovascular, renal, and respiratory therapeutic areas.

Q5: Is prior CRO or sponsor experience required?
Yes, prior experience in clinical monitoring or trial management is preferred.

Q6: What is the last date to apply?
Applications close on 14 November 2025.

---

Summary Table

Category	Details
Company	AstraZeneca
Vacancy	Clinical Research Associate
Required Education	Life Sciences, Pharmacy, Nursing, Biotechnology
Experience	2–5 Years
Location	New Delhi, India
Department	Clinical Operations / Research
Job Type	Full-Time, On-site
Application Deadline	14 November 2025
Apply Link	Apply Here