SMO Clinical Research (India) Private Limited is inviting applications for the Clinical Research Coordinator (CRC) position at its Sadashivanagar, Bangalore location. This opportunity is suitable for candidates from a Life Science background with clinical research experience who want to build or advance their career in clinical trial operations.
As a Clinical Research Coordinator, the selected candidate will support clinical studies from initiation through completion, coordinate with investigators and study teams, maintain essential clinical trial documentation, assist with participant-related activities, and help ensure studies are conducted according to protocols, Good Clinical Practice (GCP), SOPs, and applicable regulatory requirements.
SMO Clinical Research CRC Job Overview
Company: SMO Clinical Research (India) Private Limited
Position: Clinical Research Coordinator (CRC)
Location: Sadashivanagar, Bangalore, Karnataka
Qualification: Any Life Science background
Experience: Clinical research experience preferred/required as per the recruitment announcement
Job Function: Clinical Research / Clinical Trial Operations
Employment Type: Full-Time
Clinical Research Coordinator Responsibilities
The Clinical Research Coordinator will provide operational and administrative support for clinical research studies. Key responsibilities include:
- Coordinate and support clinical research studies from study initiation through completion.
- Maintain study documentation, regulatory files, essential documents, and clinical trial records.
- Coordinate activities between investigators, study participants, sponsors, and clinical research teams.
- Support participant recruitment, screening, enrollment-related activities, and follow-up.
- Ensure study activities comply with approved protocols, Good Clinical Practice (GCP), SOPs, and applicable regulations.
- Assist with clinical study data collection and documentation.
- Support accurate and timely eCRF (Electronic Case Report Form) data entry.
- Help maintain study records and documentation required for effective clinical trial management.
Qualification and Eligibility
Candidates interested in the Clinical Research Coordinator job in Bangalore should meet the requirements mentioned in the hiring announcement.
Educational Qualification: Candidates from any Life Science background can be considered, with priority given to applicants who have relevant clinical research experience.
Candidates with academic backgrounds related to life sciences, pharmacy, biotechnology, microbiology, clinical research, or allied disciplines may consider applying where their qualifications and experience align with the employer’s requirements.
Applicants should ideally understand clinical research fundamentals, clinical trial documentation, study protocols, GCP principles, participant coordination, and clinical data documentation.
Skills Relevant for CRC Jobs
Candidates applying for this Clinical Research Coordinator vacancy can benefit from knowledge or experience in:
- Clinical trial coordination
- Good Clinical Practice (GCP)
- Clinical study documentation
- Essential and regulatory files
- Patient/participant coordination
- Screening and follow-up
- Study protocol compliance
- eCRF data entry
- Clinical data collection
- Investigator and sponsor coordination
- SOP compliance
Why Consider This Clinical Research Coordinator Role?
This opportunity provides exposure to several core areas of clinical trial execution. A CRC position can help professionals develop practical experience in study coordination, clinical documentation, participant management, regulatory compliance, and communication with investigators and other clinical research stakeholders.
Experience as a Clinical Research Coordinator can also provide a foundation for career progression across clinical operations and related functions, depending on an individual’s experience, qualifications, and future opportunities.
How to Apply
Interested and eligible candidates can send their updated CV/resume to:
Email: info@smo-india.com