Premier Research Hiring Site Solutions Executive (Clinical Research)
Are you seeking Premier Research Careers India or a Clinical Trial Coordinator Job in Srinagar? Globally recognized clinical research organization (CRO) Premier Research is hiring for the position of Site Solutions Executive.
This clinical trial coordination, eCRF data management, and site documentation vacancy operates full-time from a clinical site in Srinagar, Jammu & Kashmir. The role is open to candidates holding a Bachelor's or Master's degree in Clinical Sciences, Biological Sciences, Mathematical Sciences, Life Sciences, Nursing, MBBS, or BDS. Candidates with 1 to 4 years of experience in clinical operations or site management are preferred, though profiles with 4+ years of direct site experience without these degrees will also be considered. The executive will enter CRF data, organize Trial Master File (TMF) logs, coordinate regulatory documentation, and scheduling patient visits. To write a resume detailing your patient recruitment metrics, ethics committee submissions, or GCP compliance trackers, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Premier Research |
| Position | Site Solutions Executive |
| Job Requisition ID | R6461 |
| Job Location | Srinagar, Jammu & Kashmir, India |
| Work Mode | On-site / Office-Based |
| Department | Clinical Operations |
| Experience Required | 1 – 4 Years in clinical trial coordination (or 4+ years site experience) |
| Qualifications | Bachelor’s / Master's degree in Life Sciences, Nursing, BDS, MBBS |
💼 Key Responsibilities
- Site Coordination: Coordinate daily clinical trial operations at the research site under the protocol.
- GCP Compliance: Ensure clinical activities comply with ICH-GCP guidelines, protocol rules, and local regulations.
- PI Support: Assist the Principal Investigator (PI) in screening, enrolment, dosing, and patient visit scheduling.
- eCRF Data Entry: Perform timely data entry of Case Record Forms (CRF) and Electronic CRFs (eCRF).
- TMF Oversight: Maintain the Trial Master File (TMF) and essential study folders on-site.
- Ethics Submissions: Coordinate submissions of protocols, adverse events, and periodic reports to the Ethics Committee.
- Monitoring visits: Prepare site documents for monitoring visits, sponsor audits, QA checks, and regulatory inspections.
To learn how clinical operations coordinators and site solution specialists salaries compare to conventional pharmacovigilance safety analyst and clinical programming tracks, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master's degree in clinical, biological, or mathematical sciences, or a medical/dental/nursing qualification.
- Alternative Entry: Candidates with 4+ years of clinical research site experience can apply without the science degree.
- GCP Guidelines: Strong knowledge of Good Clinical Practice (GCP) guidelines, site protocols, and documentation auditing.
- Communication: Good oral and written communication skills in English and at least one local Indian language.
- Database Skills: Experience working with eCRF portals and managing site patient registries.
For pharmacy and biological science graduates evaluating clinical operations pathways compared to conventional laboratory quality control or chemical formulation careers, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Premier Research?
- Work for a global leader supporting biotech, medtech, and specialty pharma trials.
- Obtain exposure to international clinical trial regulations and quality standards.
- Excellent career growth tracks inside clinical operations and management.
- Collaborative workplace environment that supports ongoing technical training.
To review your basic knowledge of patient registries, clinical trial structures, and GCP guidelines before your screening assessments, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 Site Solutions vs Healthcare IT
Premier Research Site Solutions Executives coordinate trial sites, manage investigator databases, and audit eCRF records, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Premier Research Candidates
- Highlight Therapeutic Focus: Detail the specific studies (oncology, rare disease, neurology) you coordinated on-site.
- Specify eCRF Tools: Name the clinical databases (Rave, Inform, Oracle Clinical) you have worked with.
- Document Visit History: Mention the number of site initiation, monitoring, or close-out audits you assisted with.
💬 Premier Research Site Solutions Executive Interview Questions
- Q1. How do you prepare a clinical site for a monitor's visit?
Answer Guidance: I ensure all data entry in the eCRF is up to date, resolve outstanding queries, organize investigator site files (ISF), confirm investigational product (IP) logs are reconciled, and schedule time with the PI. - Q2. What are the key elements of an Informed Consent Form (ICF) process?
Answer Guidance: The ICF process must be voluntary, documented, and completed before any protocol-related procedure. It requires explaining study risks, benefits, and patient rights, followed by signing and dating by the subject and the person obtaining consent. - Q3. How do you handle a serious adverse event (SAE) at the site level?
Answer Guidance: I immediately inform the Principal Investigator, assist in documenting all clinical details, complete the SAE form, and ensure it is submitted to the sponsor and Ethics Committee within 24 hours of site awareness.
📖 How to Apply?
Before submitting your application, please read the step-by-step guidance on how to navigate the registration portal, fill out required forms, and format your application profile:
📄 Premium ATS Resume Builder Service
Want to build a professional ATS-friendly resume tailored for Clinical Site Operations, Trial Coordination, or Clinical Operations roles? Message us directly on our LinkedIn Company Page with the phrase "I want Resume Builder Service", and our expert team will connect with you:
📲 Message Us on LinkedIn🚀 Direct Application Links
If you are ready with your resume and profile documents, submit your application directly via the official recruitment boards:
Apply Online – Premier Research Workday Board❓ Frequently Asked Questions
Q. Where is this clinical site position located?
This is an on-site, office-based role located at one of the research sites in Srinagar, India.
Q. Can I apply if I don't have a science graduation degree?
Yes, candidates with a minimum of 4 years of experience working directly at clinical research sites are eligible without a science degree.
Q. What is the required local language skill?
Candidates should be fluent in English and at least one local Indian language spoken in Srinagar.
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