Premier Research
Healthcare
SiteSolutionsExecutive(PRI)
Neural analysis suggests this role is
optimal for Mid+ candidates.
“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.
Problem-solving; Analytical skills
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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