CYTENET SMO Ahmedabad present an excellent career opportunity for candidates with backgrounds in Pharmacy, Life Sciences, Biotechnology, Nursing, and Healthcare. If you have 1–1.5 years of clinical research experience, this full-time position offers valuable exposure to clinical trials, regulatory compliance, patient management, and sponsor interactions.
As India’s clinical research industry continues to expand, Clinical Research Coordinator jobs remain among the most sought-after career options for pharmacy and life science professionals. This opportunity at CYTENET SMO allows candidates to build expertise in ICH-GCP guidelines, clinical trial documentation, ethics committee submissions, and patient safety while working on industry-sponsored clinical studies.
Job Highlights
| Particular | Details |
|---|---|
| Organization | CYTENET SMO |
| Position | Clinical Research Coordinator (CRC) |
| Job Location | Ahmedabad, Gujarat |
| Job Type | Full-Time |
| Vacancies | 01 |
| Experience | 1–1.5 Years Preferred |
| Industry | Clinical Research |
Eligibility Criteria
Candidates with the following qualifications are eligible to apply:
- B.Pharm
- M.Pharm
- B.Sc Life Sciences
- M.Sc Biotechnology
- M.Sc Microbiology
- Biochemistry
- Zoology
- Botany
- Nursing
- BAMS
- BHMS
- BDS
- Other Healthcare-related Degrees
Experience Required
- 1–1.5 years in Clinical Research or Site Management Organization (SMO) preferred.
Clinical Research Coordinator Responsibilities
Selected candidates will perform the following duties:
- Coordinate day-to-day clinical trial activities.
- Manage patient recruitment and screening.
- Support informed consent documentation.
- Schedule and coordinate patient visits.
- Maintain Clinical Research Forms (CRFs).
- Update Electronic Data Capture (EDC) systems.
- Ensure protocol compliance and ICH-GCP adherence.
- Prepare Ethics Committee submissions.
- Assist investigators during monitoring visits.
- Maintain Investigator Site Files (ISF).
- Document Adverse Events (AE) and Serious Adverse Events (SAE).
- Coordinate with sponsors, CROs, investigators, and hospital staff.
- Support audit and inspection readiness.
Required Skills
Candidates should possess:
- Knowledge of ICH-GCP Guidelines
- Clinical Trial Documentation
- Regulatory Compliance
- Microsoft Office
- Time Management
- Communication Skills
- Teamwork
- Organizational Skills
- Attention to Detail
Preferred Technical Knowledge
- Case Report Forms (CRF)
- Electronic Data Capture (EDC)
- CTMS Software
- Source Documentation
- Ethics Committee Process
- SAE Reporting
- Monitoring Visits
Why Join CYTENET SMO?
Working with CYTENET SMO offers professionals an opportunity to gain practical exposure to:
- Global Clinical Trials
- Site Management Operations
- Regulatory Documentation
- Sponsor and CRO Interaction
- Professional Training
- Career Development
- Clinical Operations
Career Growth After CRC
A Clinical Research Coordinator can progress into roles such as:
- Senior Clinical Research Coordinator
- Clinical Research Associate (CRA)
- Senior CRA
- Lead CRA
- Clinical Trial Manager
- Project Manager
- Clinical Operations Manager
Professionals may also transition into:
- Pharmacovigilance
- Regulatory Affairs
- Medical Writing
- Clinical Data Management
- Medical Monitoring
Salary
Although the official salary has not been disclosed, professionals with 1–2 years of Clinical Research Coordinator experience in Ahmedabad can expect an estimated annual salary ranging from:
₹3.5 LPA – ₹5.5 LPA
Salary may vary depending on experience, qualifications, and interview performance.
How to Apply
Interested candidates should:
- Update their latest resume.
- Include educational qualifications and clinical research experience.
- Mention technical skills and certifications.
- Send their application to:
📧 Email: info@cytenet.org