Takeda Hiring Senior Clinical Research Associate in Mumbai for experienced CRAs with global clinical trials and ICH-GCP expertise.
About the Company
Takeda is a global, values-driven biopharmaceutical organization focused on discovering and delivering life-transforming treatments. The company’s research and development efforts span oncology, rare diseases, neuroscience, gastroenterology, and vaccines. Takeda Hiring Senior Clinical Research Associate
Takeda’s Global Portfolio Division is recognized for its strong clinical governance, rigorous quality standards, and strict adherence to ICH-GCP and global regulatory requirements. Employees at Takeda benefit from long-term career stability, global exposure, and the opportunity to contribute to meaningful advancements in patient care worldwide.
Job Details
- Job Title: Senior Clinical Research Associate (Senior CRA)
- Department: Research & Development – Global Portfolio Division
- Employment Type: Full-time, Permanent
- Job Location: Mumbai, Maharashtra, India
- Experience Required: 5+ years
Job Description
Takeda is hiring a Senior Clinical Research Associate to support its global clinical development programs. This role is designed for experienced CRAs with strong independent monitoring capabilities and a deep understanding of international clinical trial regulations.
The Senior CRA will be responsible for ensuring that clinical trials are conducted in compliance with study protocols, regulatory guidelines, and Takeda’s internal standards while maintaining the highest levels of data integrity and patient safety. Takeda Hiring Senior Clinical Research Associate
Skills / Qualifications
Educational Qualifications
Candidates must hold one of the following:
- Master’s Degree in Life Sciences, Pharmacy, Clinical Research, or Healthcare
- PhD in a relevant scientific discipline
Experience Requirement
- Minimum 5+ years of experience as a Clinical Research Associate
- Consistent and strong performance record over the past 2–3 years
Required Skills & Competencies
- In-depth knowledge of ICH-GCP and local/international clinical trial regulations
- Strong analytical, organizational, and problem-solving skills
- Excellent communication, interpersonal, and stakeholder management abilities
- Ability to independently manage multiple sites and studies
- Experience in CRO oversight and cross-functional collaboration
Takeda Hiring Senior Clinical Research Associate
Key Responsibilities
- Perform site selection, initiation, routine monitoring, and close-out visits
- Ensure compliance with study protocols, ICH-GCP, local regulations, and Takeda SOPs
- Evaluate site practices to maintain subject safety, data quality, and regulatory compliance
- Track regulatory submissions, approvals, enrollment, and study milestones
- Review CRF completion, data entry accuracy, and timely query resolution
- Ensure proper maintenance of essential documents in the Trial Master File (TMF)
- Maintain full adherence to monitoring plans and study timelines
- Support audits, inspections, CAPAs, and quality improvement activities
- Provide CRO oversight in collaboration with clinical operations leadership
- Monitor study budgets and ensure financial compliance
- Communicate study progress and issues to internal and external stakeholders
Takeda Hiring Senior Clinical Research Associate
Benefits / Perks
- Opportunity to work on global, high-impact clinical trials
- Exposure to international clinical development programs
- Structured career growth and leadership pathways
- Strong emphasis on ethics, quality, and patient safety
- Competitive compensation aligned with global standards
- Stable and long-term career environment
Takeda Hiring Senior Clinical Research Associate
Why You Should Join
Joining Takeda as a Senior CRA allows you to work at the forefront of global clinical research while contributing to therapies that improve and save lives. The role offers professional growth, international exposure, and the chance to collaborate with world-class clinical research teams while maintaining high ethical and quality standards. Takeda Hiring Senior Clinical Research Associate
Frequently Asked Questions (FAQs)
Is this role suitable for entry-level CRAs?
No. This is a senior-level position requiring a minimum of 5 years of CRA experience.
Does this role involve extensive travel?
Yes. Domestic travel of approximately 20–30% and limited international travel may be required.
Will this role involve CRO oversight?
Yes. The position includes CRO oversight responsibilities in coordination with clinical operations teams.
What therapeutic areas will I work on?
The role supports multiple global R&D programs across Takeda’s therapeutic portfolio.
What career growth opportunities are available after this role?
Future roles may include Lead CRA, Clinical Operations Manager, and global clinical study leadership positions.
How to Apply
Interested and eligible candidates should apply through Takeda’s official careers portal using the link below. Ensure all application details are accurate and complete before submission. Takeda Hiring Senior Clinical Research Associate
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