Clinical Research Associate II Hiring at Emmes Group
- Explore an Exciting Opportunity as a Clinical Research Associate II in Bengaluru
- About Emmes Group
- Job Role: Clinical Research Associate II
- Key Responsibilities
- Qualifications and Skills Required
- Educational Background:
- Experience:
- Additional Skills:
- Why Join Emmes Group?
- How to Apply
- Courses That Fit This Role
- Quick Overview Table
Clinical Research Associate II Job for BSc, MSc Graduates in Bengaluru – Apply Now!
Apply for Clinical Research Associate II at Emmes Group in Bengaluru. Open for BSc/MSc graduates with 1-2 years of experience. Clinical Operations role.
Explore an Exciting Opportunity as a Clinical Research Associate II in Bengaluru
Are you a BSc or MSc graduate with 1-2 years of experience in clinical research? Emmes Group is offering an exceptional opportunity to join as a Clinical Research Associate II (CRA II) in Bengaluru. This role involves working in Clinical Operations, providing monitoring and oversight for critical clinical trials. If you’re passionate about advancing medical discoveries and want to be part of a purpose-driven team, this could be your ideal role.
About Emmes Group
With a legacy spanning over 47 years, Emmes Group has established itself as a key clinical research partner for both public and private sectors. With expertise in vaccines, rare diseases, neuroscience, and more, Emmes is committed to transforming lives through science. The company offers a collaborative culture that blends performance with a strong people focus.
Job Role: Clinical Research Associate II
Key Responsibilities
Monitoring & Site Management
- Conduct remote and on-site monitoring visits including site initiation, interim, and closeout visits.
- Perform source data verification, informed consent review, and compliance checks.
- Document findings in detailed monitoring reports and oversee post-visit actions.
Collaboration & Support
- Act as a point of contact for study sites, supporting resolution of issues.
- Provide site training in GCP, protocol adherence, and reporting procedures.
- Assist in audit preparations and participate in investigator meetings.
Compliance & Documentation
- Ensure trials are conducted as per ICH GCP, SOPs, and regulatory standards.
- Contribute to development and review of study-related documentation.
Qualifications and Skills Required
Educational Background:
- Bachelor’s or Master’s degree in Life Sciences or relevant scientific discipline
Experience:
- 1-2 years of monitoring experience (remote and onsite)
Additional Skills:
- Proficient in MS Office
- Strong communication, critical thinking, and organizational skills
- Familiar with clinical research regulations and ICH-GCP guidelines
Why Join Emmes Group?
- Strong industry presence with decades of clinical research experience
- Exposure to global clinical trials and cutting-edge research areas
- Collaborative team culture with professional development opportunities
- Remote work options available from Ahmedabad, New Delhi, and other locations
How to Apply
Ready to make a difference in the field of clinical research?
👉 Click here to apply now
Courses That Fit This Role
- BSc. Life Sciences
- MSc. Clinical Research
- BSc. Microbiology
- MSc. Biotechnology
- B Pharm / M.Pharm (optional if life science focused)
Quick Overview Table
| Company Name | Current Vacancies in Departments | Required Education | Experience Required |
|---|---|---|---|
| Emmes Group | Clinical Operations (CRA II) | BSc/MSc in Life Sciences | 1-2 Years |
To apply for this job please visit careers.emmes.com.