Premier Research Hiring Associate Analyst (PRI) – Fully Remote
Are you seeking remote clinical research jobs in India, CRO site start-up analyst vacancies, or regulatory feasibility coordinator careers? Leading global Contract Research Organization (CRO) Premier Research is hiring an Associate Analyst (PRI) for its clinical operations team under a 100% remote (work-from-home) model.
This clinical study feasibility screening, site start-up support, Confidential Disclosure Agreement (CDA) management, Investigator Site File (ISF) auditing, and electronic Trial Master File (eTMF) validation vacancy operates under a fully remote model, with Bangalore as the base location. The position is open to life sciences, nursing, and pharmacy graduates holding a Bachelor's or Master's degree. Candidates must possess 1 to 3 years of experience in clinical trial operations, site start-up, feasibility, or project coordination. To draft a professional ATS-friendly resume detailing your site trackers, TMF validations, or study metrics reporting, check our guide on how to apply for healthcare and pharma jobs online.
📋 Job Overview
- Company: Premier Research
- Position: Associate Analyst (PRI)
- Job Requisition ID: R6479
- Job Location: Fully Remote (Work From Home, Base: Bangalore, India)
- Employment Type: Full-Time
- Experience: 1 – 3 Years in Clinical Operations / Site Start-up
- Qualification: Bachelor's / Master's degree in Pharmacy, Life Sciences, Biotech, or Nursing
- Expected CTC: ₹6,50,000 – ₹10,00,000 per annum
💼 Key Responsibilities
- Site Feasibility Support: Gather study information from sponsors, prepare Confidential Disclosure Agreements (CDAs), and compile feasibility questionnaires.
- Start-Up Coordination: Monitor start-up milestones, coordinate with site monitors, and track approvals for essential investigator site files.
- eTMF & ISF Auditing: Review, validate, and upload essential regulatory documentation into the electronic Trial Master File (eTMF) to support audit readiness.
- Feasibility Communications: Serve as a central communication link between biotech sponsors, CRO project managers, and clinical research sites.
- Study Trackers Management: Maintain site select spreadsheets, track patient recruitment metrics, and verify eCRF compliance timelines.
- Finance Support: Assist project teams in coordinating investigator site payments and patient reimbursements.
To learn about clinical trials, monitoring frameworks, and trial site management structures, read our detailed Clinical Research Coordinator (CRC) Guide.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master's degree in Pharmacy, Life Sciences, Biotechnology, Nursing, or related disciplines.
- Experience: 1 to 3 years of active clinical research experience, with a focus on site start-up, feasibility, or project coordination.
- TMF Proficiency: Understanding of essential document collection, review checklists, and eTMF software tools.
- Communication: Good written and verbal English communication skills for collaborating with global sponsor and investigator teams.
- Software Skills: Proficiency in Microsoft Excel, PowerPoint, Word, and clinical trial tracking systems.
- Ownership: Ability to work independently and manage project trackers under remote work disciplines.
To practice your knowledge of GCP parameters, regulatory documentation files, and trial roles before your screening rounds, try our interactive Clinical Trial Assistant (CTA) Quiz.
🎁 Why Join Premier Research?
- 100% remote working model, allowing you to build your career from home.
- Obtain direct exposure to global clinical operations and advanced study feasibility processes.
- Partner with innovative biotechnology and specialty pharmaceutical sponsors.
- Access structured training programs and career progression pathways.
To evaluate your skills in clinical operations and monitor coordination concepts, try our Clinical Research Associate (CRA) Assessment Quiz.
📝 Resume Tips for Premier Research Candidates
- Detail Document Tasks: Mention experience with CDAs, feasibility logs, investigator site files, and Greenlight approvals.
- Highlight Software Experience: Clearly list any eTMF systems, CTMS databases, or tracking spreadsheets you have managed.
- Use Target Keywords: Include terms like Site Activation, Study Feasibility, Essential Documents, TMF validation, and ICH-GCP.
💬 Premier Research Associate Analyst Interview Questions
- Q1. What is a Confidential Disclosure Agreement (CDA) and why is it used in study start-up?
Answer Guidance: A CDA (also called a Non-Disclosure Agreement or NDA) is a legal contract between the sponsor/CRO and the clinical site. It is executed before sharing confidential details about the study protocol to ensure that the site does not disclose proprietary information. - Q2. What is the difference between a Feasibility Questionnaire and a Site Selection Visit?
Answer Guidance: A feasibility questionnaire is a survey sent to potential sites during the early planning phase to evaluate their patient population, facility equipment, and investigator interest. A Site Selection Visit (SSV) is an in-person or remote meeting conducted after reviewing questionnaires to physically verify the site's capabilities before final activation. - Q3. How do you handle missing essential documents during eTMF audit reviews?
Answer Guidance: I document the discrepancy in our tracking tool, notify the Clinical Research Associate (CRA) or site coordinator, provide a clear timeline for document recovery, and verify the updated file against our checklist before archiving it in the eTMF database.
📖 How to Apply?
Before submitting your application, please read our step-by-step guidance on how to navigate the Workday 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 Study Feasibility, Site Start-up, or Clinical Analysis 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 Link
If you are ready with your documents, apply directly via the official Premier Research Workday careers portal:
Apply Online – Premier Research Careers (Associate Analyst PRI)📄 Try Free ATS Resume Analyzer & Builder
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🚀 Launch Free ATS Resume Tool❓ Frequently Asked Questions
Q. Is this Associate Analyst role remote?
Yes, this is a 100% remote (work-from-home) clinical operations position within India.
Q. What is the required experience for this Premier Research job?
Candidates must have between 1 to 3 years of clinical operations, feasibility, site start-up, or trial tracking experience.
Q. What fields of study are eligible?
A Bachelor's degree in Pharmacy, Life Sciences, Biotechnology, Nursing, or related disciplines is required.
