Takeda Hiring Senior Clinical Research Associate
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Experience Requirement
- Required Skills & Competencies
- Location & Salary
- Travel Requirements
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for entry-level CRAs?
- Does this role involve extensive travel?
- Will this role involve CRO oversight?
- What therapeutic areas will I work on?
- What is the career growth after this role?
- Job Summary Table
Takeda hiring Senior Clinical Research Associate in Mumbai. Master’s/PhD with 5+ years CRA experience eligible. Global R&D role.
Takeda is hiring a Senior Clinical Research Associate (Senior CRA) for its Research & Development division in Mumbai, Maharashtra. This role is targeted at experienced clinical research professionals who have strong hands-on monitoring expertise and a deep understanding of global clinical trial regulations. The position offers the opportunity to work on complex, high-impact clinical studies while contributing directly to Takeda’s mission of delivering life-transforming treatments to patients worldwide.
Company Overview
Takeda is a global, values-driven biopharmaceutical company committed to discovering and delivering life-changing therapies. With a strong focus on oncology, rare diseases, neuroscience, gastroenterology, and vaccines, Takeda operates across the full spectrum of research, development, and commercialization.
Takeda’s Global Portfolio Division plays a critical role in advancing innovative clinical programs while maintaining the highest standards of ethics, quality, and patient safety. The organization is known for its robust clinical governance, strong CRO oversight models, and strict adherence to ICH-GCP and global regulatory standards. Working at Takeda provides long-term career stability, global exposure, and the opportunity to contribute to meaningful healthcare advancements.
Job Role & Responsibilities
As a Senior Clinical Research Associate, you will be responsible for independent site monitoring and study management activities to ensure clinical trials are conducted in compliance with study protocols, regulatory requirements, and Takeda standards.
Key Responsibilities
- Perform site monitoring visits including site selection, initiation, routine monitoring, and close-out visits
- Ensure clinical trial conduct complies with study protocols, ICH-GCP, local regulations, and Takeda SOPs
- Evaluate site practices to ensure data integrity, subject safety, and regulatory compliance
- Track regulatory submissions, site approvals, recruitment, enrollment, and study milestones
- Monitor CRF completion, data entry, and timely resolution of data queries
- Ensure essential documents are filed correctly in the Trial Master File (TMF)
- Maintain 100% adherence to the monitoring plan and study timelines
- Support clinical quality activities including CAPAs, audit responses, and inspection readiness
- Provide CRO oversight in collaboration with Clinical Operations Leads and Managers
- Monitor study budgets and ensure financial adherence for assigned trials
- Communicate study updates to internal and external stakeholders as per defined timelines
This role plays a vital part in maintaining trial quality, regulatory compliance, and successful delivery of global clinical development programs.
Eligibility / Qualifications
Required Education
Candidates must possess one of the following qualifications:
Master’s Degree in Life Sciences, Pharmacy, Clinical Research, Healthcare, PhD in Scientific Discipline
Experience Requirement
- Minimum 5+ years of experience as a Clinical Research Associate in the clinical trials industry
- Proven and stable performance record over the past 2–3 years
Required Skills & Competencies
- Strong working knowledge of ICH-GCP and local clinical trial regulations
- Excellent organizational, analytical, and problem-solving skills
- Superior communication, interpersonal, negotiation, and stakeholder management abilities
- Ability to work independently while managing multiple sites and studies
- Experience in CRO oversight and cross-functional collaboration
Location & Salary
- Job Location: Mumbai, Maharashtra, India
- Employment Type: Full-time, Regular
- Department: Research & Development (Global Portfolio Division)
Salary details are not disclosed and will be aligned with Takeda’s compensation structure based on experience and role scope.
Travel Requirements
- Domestic travel: Approximately 20–30%, including occasional weekends
- International travel: Approximately 10–20%, based on study requirements
Application Process
Interested and eligible candidates can apply directly through Takeda’s official careers portal:
Apply Here: https://jobs.takeda.com/job/-/-/1113/90306745136
Candidates are encouraged to ensure all information submitted during the application process is accurate and complete.
Frequently Asked Questions (FAQs)
Is this role suitable for entry-level CRAs?
No. This is a senior-level role requiring 5+ years of CRA experience.
Does this role involve extensive travel?
Yes. Domestic travel of 20–30% and limited international travel may be required.
Will this role involve CRO oversight?
Yes. The role includes CRO oversight responsibilities in coordination with clinical operations leadership.
What therapeutic areas will I work on?
The role supports global R&D programs across Takeda’s therapeutic portfolio.
What is the career growth after this role?
Career progression includes Lead CRA, Clinical Operations Manager, and Global Clinical Study roles.
Job Summary Table
| Company | Takeda |
|---|---|
| Vacancies | Senior Clinical Research Associate |
| Required Education | Master’s Degree, PhD in Life Sciences / Healthcare |
| Experience | 5+ Years |
To apply for this job please visit jobs.takeda.com.
