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Site Solutions Executive (Pri) - Delhi, India

4+ years
3-6 LPA
Delhi, New Delhi, India
10 June 11, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Site Solutions Executive (PRI) – Delhi, India
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Type: Office-Based (Full-Time)
Location: India (Delhi Region)
Requisition ID: R6221
Posted: Recently

Premier Research is seeking a Site Solutions Executive (PRI) to join our India Operations team in Delhi. In this role, you will contribute to advancing biotech, medtech, and specialty pharma innovations that help bring new medicines, devices, and diagnostics to patients faster. Our work is deeply connected to improving and saving lives, and our people are central to our success.

We are committed to supporting your professional growth, offering opportunities to build skills, develop your career, and maintain a healthy work-life balance. At Premier Research, your ideas are valued, and your contributions directly influence how we work and deliver impact.

Key Responsibilities
As part of the clinical research site team, you will:

  • Coordinate and support clinical trial activities at the site, ensuring adherence to study protocols, GCP guidelines, and applicable regulatory requirements

  • Assist the Principal Investigator (PI) and study team in ensuring sponsor and regulatory compliance across all trial activities

  • Review site processes, identify gaps, and support implementation of improved workflows

  • Perform timely entry of Case Report Forms (CRF/eCRF) in coordination with the PI or investigator

  • Maintain essential clinical trial documentation, including the Trial Master File (TMF)

  • Support site initiation, monitoring, and close-out visits, as well as patient visits, QA audits, sponsor visits, and inspections

  • Report site performance metrics as required

Candidate Profile
We are looking for candidates who have:

  • A Bachelor’s or Master’s degree in clinical, biological, mathematical sciences, or related fields; or a medical, dental, or nursing qualification

    • Alternatively, at least 4 years of experience working in clinical research site environments may be considered

  • Strong written and verbal communication skills in English and at least one Indian local language

  • Proficiency in Hindi and English (reading and writing is mandatory)

  • Excellent interpersonal, coordination, and organizational abilities

  • Strong attention to detail with a focus on data accuracy and documentation

  • Analytical and problem-solving skills

  • Awareness of ethical standards, patient safety, and regulatory requirements in clinical research

  • Basic proficiency with computers and office tools

Additional Requirement

  • Must be available to join on or before June 14, 2026

  • Role is based in the Delhi region, India