Premier Research has announced a new Site Solutions Executive vacancy in Srinagar, India. This office-based clinical research opportunity is ideal for candidates with backgrounds in Life Sciences, Clinical Research, Nursing, Medicine, Dentistry, or related healthcare disciplines who are looking to build a career in clinical trial operations.
The selected candidate will work directly with investigators and research sites to coordinate clinical trial activities, ensure regulatory compliance, maintain study documentation, and support successful execution of sponsor-sponsored clinical studies.
If you’re searching for Clinical Research Jobs in India, Site Solutions Executive Jobs, or Clinical Trial Coordinator Jobs 2026, this opportunity offers hands-on exposure to global clinical trials within a leading CRO.
Job Details
| Particular | Details |
|---|---|
| Company | Premier Research |
| Position | Site Solutions Executive |
| Location | Srinagar, India |
| Job Type | Full-Time |
| Work Mode | Office-Based |
| Department | Clinical Operations |
| Job ID | R6461 |
Key Responsibilities
The selected candidate will:
- Coordinate day-to-day clinical trial activities at the research site.
- Ensure compliance with study protocols, ICH-GCP guidelines, and local regulations.
- Support the Principal Investigator (PI) and study team throughout trial execution.
- Perform timely CRF/eCRF data entry and maintain data quality.
- Maintain Trial Master File (TMF) and essential study documentation.
- Prepare and support site initiation, monitoring, close-out, QA, sponsor, and inspection visits.
- Coordinate ethics committee submissions and regulatory documentation.
- Schedule patient visits, screening, enrolment, investigations, and assessments.
- Coordinate laboratory sample collection and logistics.
- Maintain communication between investigators, sponsors, CROs, and monitors.
- Track and report site performance metrics.
- Support patient awareness programs and clinical research outreach activities.
- Assist in feasibility studies, epidemiological data collection, and patient database creation.
Eligibility Criteria
Candidates should possess any one of the following qualifications:
- Bachelor’s Degree in Clinical Sciences
- Bachelor’s Degree in Biological Sciences
- Bachelor’s Degree in Mathematical Sciences
- Life Sciences Degree
- Nursing Qualification (B.Sc Nursing/GNM)
- MBBS
- BDS
- Master’s Degree in related disciplines
OR
Candidates with 4+ years of experience working at clinical research sites may also be considered if they do not meet the above educational requirements.
Required Skills
- Clinical Trial Coordination
- Good Clinical Practice (ICH-GCP)
- eCRF & CRF Management
- Trial Master File (TMF)
- Ethics Committee Documentation
- Clinical Site Management
- Patient Recruitment & Scheduling
- Clinical Documentation
- Regulatory Compliance
- Strong Communication Skills
- English and one local Indian language
- Organizational & Analytical Skills
- Attention to Detail
Why Join Premier Research?
Premier Research is a globally recognized Clinical Research Organization (CRO) supporting biotechnology, pharmaceutical, and medical device companies in bringing innovative therapies to patients.
Employees receive:
- Opportunity to work on global clinical trials
- Exposure to international regulatory standards
- Career growth within clinical operations
- Collaborative and supportive work environment
- Training and professional development
- Meaningful contribution to patient-focused research
How to Apply
