Premier Research is hiring for two Site Solutions Executive positions in its India Operations team, with office-based, full-time opportunities in Calicut and Bangalore. Eligible candidates with a degree in clinical, biological or mathematical sciences, or related fields, can apply for these clinical research site operations roles.

The positions involve coordinating clinical trial activities, maintaining trial documentation, supporting Principal Investigators, managing ethics committee submissions, and ensuring compliance with study protocols, Good Clinical Practice (GCP) guidelines, and applicable local regulations.

Premier Research Recruitment 2026: Job Details

Positions Available

1. Site Solutions Executive – Calicut

• Location: Calicut
• Job Requisition ID: R7011
• Work Mode: Office-Based
• Employment Type: Full-time

Apply Online: Site Solutions Executive – Calicut

2. Site Solutions Executive – Bangalore

• Location: Bangalore
• Job Requisition ID: R7007
• Work Mode: Office-Based
• Employment Type: Full-time

Apply Online: Site Solutions Executive – Bangalore

Job Responsibilities

Selected candidates will support clinical trial execution and site operations, working with Principal Investigators (PIs), site study teams, sponsors, and Contract Research Organizations (CROs).

Key responsibilities include:

• Coordinating clinical trial activities at the site in compliance with study protocols, GCP guidelines, and local regulations.
• Supporting Principal Investigators and site study teams in meeting sponsor and regulatory requirements.
• Entering data into Case Report Forms (CRFs) and electronic Case Report Forms (eCRFs) in consultation with the investigator.
• Maintaining clinical trial documentation, including the Trial Master File (TMF).
• Preparing for and assisting with site initiation, monitoring, close-out, quality assurance, sponsor, and regulatory inspection visits.
• Coordinating ethics committee submissions for protocols, adverse events, and periodic study reports.
• Scheduling patient investigations, assessments, study visits, screening, and enrolment activities.
• Ensuring the availability, appropriate storage, and accountability of investigational products (IPs), laboratory kits, and other trial supplies.
• Coordinating laboratory sample collection and reporting.
• Supporting timely resolution of clinical trial data queries.
• Maintaining communication with site monitors, investigators, sponsors, and CRO representatives.
• Supporting feasibility assessments, site data collection, and the identification of potential study participants.
• Completing mandatory training, ongoing training modules, and standard operating procedures (SOPs).
• Supporting responses to audit findings and implementing approved recommendations with the Principal Investigator.
• Escalating systemic non-compliance or misconduct to the appropriate manager.

Eligibility and Qualifications

Candidates must meet the educational and professional requirements outlined by Premier Research.

• A Bachelor’s or Master’s degree in clinical, biological, or mathematical sciences, or a related field.
• Alternatively, a medical degree, dental degree, or nursing qualification.
• Candidates qualifying for an educational exception must have at least four years of experience working at clinical research sites.
• Good oral and written communication skills in English and at least one local Indian language.

Required Skills

Candidates should demonstrate the following skills and competencies:

• Strong interpersonal and communication skills.
• Good coordination and organizational abilities.
• Problem-solving and analytical skills.
• Attention to detail and accurate documentation.
• Understanding of the importance of data accuracy and timelines in clinical trials.
• Awareness of ethical and scientific requirements, patient safety, and patient rights.
• Familiarity with computers and office communication tools.

Application Details