Premier Research Hiring Site Solutions Executive (PRI) - Pune

🏢 Premier Research

📍 Pune, Maharashtra

🎓 Pharmacy / Life Sciences / Nursing / Medicine

💼 1 Years+ Experience

Are you seeking premium Premier Research Careers India or Site Solutions Executive Jobs in Pune? Global Contract Research Organization (CRO) Premier Research has announced recruitment for a **Site Solutions Executive (PRI)** at its Pune, Maharashtra operations. This full-time office position is open to life sciences and pharmacy graduates with 1 or more years of experience.

This role offers an excellent opportunity to manage clinical trial data entry, coordinate site-level study activities, and maintain essential trial documentation (TMF). To prepare your profile and application details, read our guide on how to apply for healthcare and pharma jobs online.

📋 Job Details

Particulars	Details
Position	Site Solutions Executive (PRI)
Company	Premier Research
Location	Pune, Maharashtra, India
Work Mode	Office-Based (Pune Office)
Employment Type	Full-Time
Experience Required	1 Years+ (Or 4+ years of site coordination experience for candidates without scientific degrees)
Qualifications	B.Pharm, M.Pharm, Pharm.D, B.Sc & M.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Nursing, MBBS, BDS, or equivalent
Department	India Operations
Job ID	R6265
Salary Range	Competitive (Based on experience)
Application Deadline	Apply Immediately (Not Mentioned)

💼 Key Responsibilities

Coordinate day-to-day clinical trial activities and general operations at study research sites.
Ensure complete compliance with study protocols, ICH-GCP guidelines, and local regulatory requirements.
Support Principal Investigators (PIs) and site coordination teams with study execution processes.
Review existing site workflows and identify opportunities for operational improvement.
Perform accurate and timely Case Report Form (CRF) and Electronic Case Report Form (eCRF) data entries.
Maintain the Trial Master File (TMF) and ensure all essential clinical trial documentation is complete.
Ensure document accuracy and regulatory readiness for sponsor audits or site monitoring visits.
Support clinical monitors (CRAs) and study sponsors with site operational requirements.
Maintain high standards of patient safety and ethical guidelines throughout study execution.

Formulating site records and completing eCRF entries require a strong command of trial protocols. Test your clinical compliance knowledge with our interactive Clinical Trial Assistant (CTA) Quiz.

🎓 Qualifications & Eligibility Criteria

Candidates possessing any of the following qualifications are eligible to apply:

Degrees: B.Pharm, M.Pharm, Pharm.D, B.Sc or M.Sc in Life Sciences, Biotechnology, Microbiology, Biochemistry, Nursing, MBBS, BDS, Medical or Dental degree, or equivalent clinical, biological, or mathematical science degrees.
Candidates without the above scientific credentials must have at least 4 years of hands-on experience working at clinical research sites.
Experience: 1 or more years of experience in clinical trial coordination or site operations.

For science and pharmacy graduates planning their career and comparing global salary development, check our guide on B.Pharm Career after Graduation: India vs USA.

Required Skills

Strong English communication skills (both written and verbal).
Reading and writing proficiency in Hindi, Marathi, and English.
Excellent site coordination, organizational, and documentation skills.
Analytical thinking, attention to detail, and problem-solving capabilities.
Basic knowledge of clinical research workflows and ICH-GCP guidelines.
Familiarity with CRF/eCRF documentation and database entry checks.
Computer proficiency, including office tools and communication software.

💰 Salary & Employee Benefits

Competitive base salary matching industry standards for mid-level clinical operations roles at Premier Research.
Opportunity to work directly with global biotechnology and pharmaceutical companies.
Direct exposure to international clinical research projects.
Supportive work environment with structured career development and training pathways.
Office-based, stable career in a leading Contract Research Organization (CRO).

To learn about typical roles and career progressions in clinical trial site operations, read our comprehensive Clinical Research Coordinator (CRC) Guide.

🌟 Why Join Premier Research?

Premier Research is a premier global CRO specializing in delivering clinical research services for innovative biotech and medical device sponsors.
Highly supportive, quality-conscious, and ethical work culture that directly contributes to improving patient lives.
Strong stepping stone to transition into Clinical Research Associate (CRA), Clinical Trial Manager (CTM), or site lead positions.

📑 Resume Tips for Premier Research

Highlight your years of experience at clinical study sites, patient recruiting, and eCRF platforms.
Emphasize your local language skills (Hindi, Marathi) which are highly preferred for coordinator roles in Maharashtra.
Ensure your CV has a clean layout, clear headers, and is optimized for Applicant Tracking Systems (ATS).

🎯 Premier Research Site Solutions Executive Interview Questions

What are the primary responsibilities of a Site Solutions Executive during study start-up?
What is the difference between an informed consent form (ICF) and an assent form?
How do you handle site documentation when a protocol amendment is issued by the sponsor?
Describe your experience with local site investigations and how you communicate with subjects.
What is GCP and what are its key principles regarding patient safety and data integrity?

📌 How to Apply?

Interested and eligible candidates can submit their applications online directly through Premier Research's official Workday job portal using the link below. Since no specific application deadline is mentioned, candidates are advised to apply immediately. For step-by-step guidance on setting up your profile, read our guide on how to apply for healthcare and pharma jobs online.