PSI CRO AG is inviting applications for the position of Clinical Research Associate II (CRA II) in Bangalore. This opportunity is suitable for experienced clinical research professionals with strong independent site monitoring experience across Phase II and/or Phase III clinical trials.
The PSI CRO CRA II job in Bangalore involves managing the clinical aspects of global clinical research projects in India, conducting onsite monitoring visits, supporting study start-up, reviewing clinical trial data, managing investigator sites, and coordinating with internal project teams.
Candidates must have at least 3 years of independent on-site monitoring experience in India and should be based in Bangalore or willing to relocate. The position also requires the ability to travel for clinical trial monitoring activities.
Key Responsibilities
As a CRA II at PSI CRO, the selected candidate will be responsible for:
- Conducting and reporting different types of onsite clinical trial monitoring visits.
- Supporting clinical study start-up activities.
- Performing Case Report Form (CRF) review.
- Conducting Source Document Verification (SDV).
- Supporting clinical data query identification and resolution.
- Facilitating clinical site budget and contract negotiations.
- Monitoring clinical trial progress at the country level.
- Managing communication and relationships with clinical trial sites and investigators.
- Serving as a point of contact for in-house support teams and external vendors.
- Communicating study progress, risks and site-level developments to internal project teams.
- Participating in clinical trial feasibility assessments.
- Supporting regulatory teams with documents required for clinical study submissions.
- Helping ensure subject rights, safety and well-being while maintaining clinical data quality and regulatory compliance.
Qualification & Eligibility
Candidates interested in the PSI CRO Clinical Research Associate II vacancy should meet the following requirements:
Education: College or university degree in Life Sciences, Pharmacy, Nursing (RN) or an equivalent combination of relevant education, training and professional experience.
Experience: At least 3 years of independent on-site clinical trial monitoring experience in India is required.
Candidates should also have experience conducting different types of monitoring visits for Phase II and/or Phase III clinical trials.
Experience with clinical trial feasibility assessments and study set-up activities is preferred.
Therapeutic-area experience in Multiple Sclerosis, Inflammatory Bowel Disease, Oncology or Infectious Diseases would be advantageous.
Applicants should have full professional proficiency in English and working knowledge of Microsoft Word, Excel and PowerPoint.
Strong planning, multitasking, communication, collaboration and problem-solving skills are important for this CRA II position.
Candidates must also be comfortable travelling as required for onsite clinical trial monitoring.
Who Can Apply?
Professionals with relevant qualifications such as B.Pharm, M.Pharm, Pharm.D, B.Sc/M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, B.Sc Nursing/M.Sc Nursing or other relevant life-science and healthcare qualifications may be considered where they meet PSI CRO’s education and experience requirements.
The key eligibility requirement is at least 3 years of independent on-site monitoring experience in India.
Preferred Clinical Research Experience
Candidates with previous exposure to the following areas may have an advantage:
- Phase II and Phase III clinical trials
- Site initiation and study start-up
- Site monitoring and management
- Source Document Verification (SDV)
- CRF review and query resolution
- Feasibility assessment
- Investigator and site communication
- Clinical trial regulatory documentation
- Site budgets and contracts
- Multiple Sclerosis
- Inflammatory Bowel Disease
- Oncology
- Infectious Diseases
Work Location
This Clinical Research Associate II position is office-based in Bangalore.
PSI CRO specifically states that applicants should either currently be based in Bangalore or be willing to relocate to Bangalore because the position requires office presence.
The role additionally involves travel for onsite clinical trial monitoring activities.
Salary
The employer has not disclosed an official salary range in the supplied job description.
For structured-data purposes, an estimated market-aligned range for an experienced CRA II in Bangalore may be approximately ₹8,00,000–₹14,00,000 per year, depending on monitoring experience, therapeutic-area expertise, current compensation and the employer’s internal salary structure.
Note: This is an estimated range and should not be interpreted as an officially disclosed PSI CRO salary.
Benefits & Career Development
PSI CRO describes this opportunity as a role that can help experienced CRAs broaden their therapeutic-area exposure and further develop clinical research expertise.
The company highlights:
- Professional development opportunities
- Training and mentorship programs
- Competitive compensation
- Comprehensive employee benefits
- Exposure to global clinical research projects
- Opportunities to expand therapeutic-area experience
- Work within an international clinical research organization
How to Apply
