Are you a Life Science graduate or postgraduate looking to build a career in clinical research? SMO Clinical Research (India) Private Limited has an opening for the position of Clinical Research Coordinator (CRC) at its Sadashivanagar, Bangalore, Karnataka location.
This opportunity is suitable for candidates with a background in Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, Nursing, Clinical Research, or related healthcare disciplines, particularly those who have prior clinical research or clinical trial site experience.
Job Overview
| Job Details | Information |
|---|---|
| Company | SMO Clinical Research (India) Private Limited |
| Position | Clinical Research Coordinator (CRC) |
| Location | Sadashivanagar, Bangalore, Karnataka |
| Qualification | Degree / Post-Graduation in Life Sciences |
| Experience | Clinical research experience preferred/required |
| Job Type | Clinical Research / Site Operations |
| Application Mode | |
| info@smo-india.com |
About the Clinical Research Coordinator Role
A Clinical Research Coordinator (CRC) is responsible for supporting the day-to-day activities of clinical trials at a research site.
The CRC generally works under the Principal Investigator (PI) and coordinates with sponsors, Clinical Research Associates (CRAs), CRO teams, ethics committees, healthcare professionals, and study participants.
The role requires strong organizational skills because the coordinator may be involved in patient recruitment, informed consent, clinical documentation, study visits, regulatory records, protocol compliance, and clinical data entry.
For candidates interested in clinical operations, this position can provide valuable practical exposure to the clinical trial environment.
Key Responsibilities
Selected candidates may be responsible for activities including:
1. Clinical Trial Coordination
- Coordinate day-to-day clinical trial activities at the research site.
- Support study activities from site initiation through study completion and close-out.
- Coordinate scheduled study visits and follow-up activities.
- Work closely with investigators and clinical research teams.
2. Patient Recruitment and Retention
- Assist with identifying and prescreening potential study participants.
- Coordinate patient visits according to the study protocol.
- Support the informed consent process under appropriate supervision.
- Maintain communication with study participants and help ensure visit compliance.
3. Regulatory and Essential Document Management
- Maintain essential clinical trial documents.
- Assist with maintaining Investigator Site Files (ISF) and regulatory documentation.
- Maintain communication and documentation related to the Ethics Committee/IEC.
- Keep study records organized and ready for monitoring or audits.
4. Data Entry and Documentation
- Collect and maintain relevant source documents.
- Enter clinical trial data accurately into electronic Case Report Forms (eCRFs).
- Respond to data queries raised by monitors or study teams.
- Ensure documentation is complete, accurate, and maintained within required timelines.
5. GCP and Protocol Compliance
- Follow the approved clinical trial protocol.
- Work according to applicable ICH-GCP guidelines and Standard Operating Procedures (SOPs).
- Follow institutional and Ethics Committee requirements.
- Support participant safety and data integrity throughout the study.
6. Communication and Coordination
The CRC may regularly communicate with:
- Principal Investigators
- Clinical Research Associates (CRAs)
- Sponsors
- CRO teams
- Ethics Committees
- Hospital/clinical staff
- Study participants
Strong communication and organizational skills are therefore important for this position.
Eligibility Criteria
Candidates interested in this opportunity should generally have:
Educational Qualification
A degree or postgraduate qualification in a Life Science or allied healthcare discipline, such as:
- B.Pharm / M.Pharm
- Biotechnology
- Microbiology
- Biochemistry
- Clinical Research
- Life Sciences
- Nursing
- Other relevant healthcare or life science disciplines
Experience
Prior experience in clinical research, clinical trial operations, site management, or a Clinical Research Coordinator role may be preferred or required.
Candidates should carefully review the employer’s requirements before applying.
Skills Required
Applicants can strengthen their profile by having knowledge or experience in:
- ICH-GCP principles
- Clinical trial documentation
- Clinical research processes
- Patient coordination
- Medical terminology
- Electronic data capture (EDC) systems
- eCRF completion
- Regulatory documentation
- Ethics Committee/IEC processes
- Good communication and interpersonal skills
- Documentation and organizational skills
How to Apply
Interested and eligible candidates can submit their updated CV/Resume directly to the company via email.
Application Email: info@smo-india.com
Candidates should make sure their resume clearly mentions:
- Highest educational qualification
- Clinical research experience
- Previous CRC/site experience, if any
- GCP certification, if applicable
- Relevant technical skills
- Current contact information
Suggested Email Subject
Application for Clinical Research Coordinator – Sadashivanagar Bangalore – [Your Name]
Before applying, candidates should verify the vacancy and requirements with the employer, as hiring requirements and openings can change.
Career Growth After CRC
A Clinical Research Coordinator position can provide valuable site-level clinical research experience and may help candidates progress toward roles such as:
- Clinical Research Associate (CRA)
- Clinical Trial Specialist
- Clinical Data Management
- Pharmacovigilance / Drug Safety
- Regulatory Affairs
- Clinical Operations
- Clinical Project Management
Frequently Asked Questions
What is the qualification for the SMO Clinical Research CRC job?
Candidates with a degree or postgraduate qualification in Life Sciences or a related healthcare discipline may be eligible. Relevant clinical research experience may also be required or preferred.
Where is the CRC position located?
The reported position is located in Sadashivanagar, Bangalore, Karnataka.
How can I apply for the CRC vacancy?
Candidates can submit their updated CV to info@smo-india.com.
Is clinical research experience required?
The vacancy information indicates that clinical research experience is preferred/required. Candidates should confirm the exact experience requirement with the hiring organization before applying.
Is this job suitable for B.Pharm or M.Pharm candidates?
Yes. Pharmacy graduates and postgraduates with relevant clinical research knowledge or experience can consider applying, subject to the employer’s eligibility requirements.
Final Takeaway
The Clinical Research Coordinator opening at SMO Clinical Research in Bangalore can be a useful opportunity for Life Science and healthcare professionals who want to develop their careers in clinical research and clinical operations.
Candidates with relevant educational qualifications, clinical trial experience, GCP knowledge, strong documentation skills, and good communication abilities should consider submitting an updated CV to the mentioned recruitment email.
Job seekers should verify the vacancy, eligibility criteria, and application details before submitting their personal information.
