Samahitha Research Solution is inviting applications for the position of Quality Control (Clinical Research) in Bengaluru, Karnataka. This opportunity is ideal for candidates with 8 months to 1 year of Quality Control, QA, or Clinical Research documentation experience, including professionals who have completed internships in a CRO environment.
If you’re looking for Clinical Research Quality Control jobs in Bengaluru, QA/QC jobs in CRO, TMF Audit jobs, or Clinical Documentation Review careers, this is an excellent opportunity to build your career with a growing clinical research organization.
Job Details
| Particular | Details |
|---|---|
| Position | Quality Control (Clinical Research) |
| Company | Samahitha Research Solution |
| Location | Bengaluru, Karnataka |
| Experience | 8 Months โ 1 Year |
| Industry | Clinical Research / CRO |
| Employment Type | Full-Time |
| Joining | Immediate Joiners Preferred |
Key Responsibilities
As a Quality Control professional, your responsibilities will include:
- Conduct Site Audits and Trial Master File (TMF) audits.
- Review monitoring reports, clinical protocols, and study documents.
- Ensure compliance with SOPs, ICH-GCP guidelines, and regulatory requirements.
- Support external audits and regulatory inspections.
- Participate in CAPA (Corrective and Preventive Action) implementation.
- Maintain and update Standard Operating Procedures (SOPs).
- Review study documentation for quality and regulatory compliance.
- Coordinate documentation review activities across clinical projects.
Eligibility Criteria
Candidates should have:
- 8 months to 1 year of experience in Quality Control.
- Internship experience in a Clinical Research Organization (CRO) is also considered.
- Educational qualification in Life Sciences, Pharmacy, Clinical Research, Biotechnology, or related fields.
- Knowledge of clinical trial documentation and regulatory compliance.
- Good communication and documentation skills.
- Strong attention to detail and analytical thinking.
Preferred Background
Applications are encouraged from candidates working as:
- Quality Assurance (QA)
- Quality Control (QC)
- Clinical Document Specialist
- Clinical Document Reviewer
- Data Reviewer
- Clinical Trial Documentation Executive
Why Join Samahitha Research Solution?
- Opportunity to work in the Clinical Research industry.
- Exposure to Site Audits and TMF Quality Reviews.
- Hands-on experience with SOP compliance and regulatory inspections.
- Career growth in Clinical Quality Assurance.
- Work with experienced Clinical Research professionals.
- Excellent learning environment for early-career candidates.
How to Apply
Interested candidates can apply using the following details:
Email: career@samahitha.com
WhatsApp: +91 80886 23642
Apply as early as possible. Immediate joiners will be given preference.
MENTION “PHARMABHARAT” IN REFERENCE
