Premier Research

Healthcare

SiteSolutionsExecutive(PRI)

₹15–25L ~AI est. Hyderabad, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Site Solutions Executive (PRI) at Premier Research. Skills: Clinical trial management, Site operations. Coordinate and facilitate all Clinical trial activities at. Ensure compliance with protocol, GCP guidelines and local”

Industry & Context.

Healthcare
Problems you'll solve

Problem-solving; Analytical skills

Eligibility Requirements

Start by 22 June 2026

What They're Looking For.

Must Have

Bachelor's or Master's degree in clinical, biological or mathematical sciences or related fields, or a medical or dental degree or a nursing, Minimum of 4 years of experience of working at clinical research sites, Good oral and written communication skills in English and at least one local Indian language, Proficiency in Hindi, Telugu and English

What You'll Do.

Coordinate and facilitate all Clinical trial activities at

Ensure compliance with protocol

GCP guidelines and local

Support Principal Investigator (PI) and site study team

Assure clinical trial(s) meet all criteria set by

Review site processes

Identify gaps in site processes

Support roll-out of site processes

Perform timely data entry of Case Record Forms

Maintain clinical trial-related documents at site

Maintain Trial Master File

How You'll Work.

Team & Collaboration

Site study team; Principal Investigator (PI)

Communication Scope

Oral communication; Written communication

Full Job Description

Premier Research is looking for a Site Solutions Executive (PRI) - Hyderabad, India to join our India Operations team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. * We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. * Your ideas influence the way we work, and your voice matters here. * As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here. **What you 'll be doing:** * Coordinates and facilitates all Clinical trial activities at site ensuring compliance with protocol, applicable GCP guidelines and local regulations. * Supports Principal Investigator (PI) and site study team assuring that the clinical trial(s) being conducted meet all the criteria set by the sponsors and regulators, * Reviews the site processes, identifies gaps and supports roll-out of site processes. * The following key functions are required routinely: Performs timely data entry of the Case Record Forms (CRF) or Electronic CRF (eCRF) in consultation with the PI/Investigator Maintaining clinical trial-related documents at site including Trial Master File. **What we are looking for:** * A bachelor’s or master’s degree in clinical, biological or mathematical sciences or related fields, or a medical or dental degree or a nursing qualification; Exceptions to this would require a minimum of 4 years of experience of working at clinical research sites. * Good oral and written communication skills in English and at least one local Indian language * Excellent interpersonal skills * Good coordination and organizational skills and also problem-solving and analytical s

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