Koncord Clinical Research Services is inviting applications for the position of In-House Clinical Research Coordinator – QC. Candidates with 2–3 years of clinical research experience, particularly on the site side, and expertise in Quality Control (QC), source/eSource documentation, and EDC platforms are encouraged to apply.
This is an excellent opportunity for Life Sciences and Pharm.D professionals seeking to build a rewarding career in clinical research while working remotely.
Job Details
| Particular | Details |
|---|---|
| Company | Koncord Clinical Research Services |
| Job Title | In-House Clinical Research Coordinator – QC |
| Job Type | Full-Time |
| Work Mode | Remote |
| Experience | 2–3 Years |
| Qualification | Life Sciences, Pharm.D |
| Department | Clinical Research – Quality Control |
| Joining | Immediate Joiners Preferred |
Key Responsibilities
The selected candidate will be responsible for:
- Perform Quality Control (QC) review of clinical research documentation.
- Verify source documents and eSource records for accuracy and completeness.
- Review data entered into Electronic Data Capture (EDC) systems.
- Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.
- Identify documentation discrepancies and coordinate with study teams for resolution.
- Maintain high-quality clinical trial documentation and data integrity.
- Support clinical operations teams in ensuring audit readiness.
- Collaborate with investigators, CRAs, and project teams during study execution.
Required Qualifications
Applicants should meet the following criteria:
- Bachelor’s or higher degree in Life Sciences or Pharm.D.
- 2–3 years of Clinical Research experience (Site-side experience preferred).
- Mandatory experience in Quality Control (QC).
- Hands-on knowledge of:
- Source Documentation
- eSource Platforms
- Electronic Data Capture (EDC) Systems
- Good understanding of ICH-GCP guidelines and clinical research processes.
- Strong attention to detail and excellent documentation skills.
- Immediate joiners will be given preference.
Why Join Koncord Clinical Research Services?
- Remote work opportunity
- Work on clinical research quality projects
- Exposure to modern eSource and EDC platforms
- Professional growth in Clinical Research Quality Assurance
- Collaborative and learning-oriented work environment
- Opportunity to contribute to high-quality clinical trials
How to Apply
Interested and eligible candidates should send their complete application along with an updated resume to:
Email: hr@koncordclinical.com
