Premier Research is hiring for two positions in its India Operations team: Site Solutions Executive (Mysore) and Site Solutions Executive Level 2. These are full-time, office-based opportunities for candidates interested in clinical research site operations and clinical trial coordination.
The selected candidates will support clinical trial activities, coordinate with Principal Investigators (PIs), maintain clinical trial documentation, facilitate site monitoring activities, and ensure compliance with Good Clinical Practice (GCP) guidelines and applicable regulations.
Candidates with qualifications in clinical, biological or mathematical sciences, medicine, dentistry or nursing can apply, subject to the experience requirements.
Premier Research Recruitment 2026 – Job Details
| Particulars | Details |
|---|---|
| Company | Premier Research |
| Job Category | Clinical Research |
| Recruitment Type | Full-Time |
| Work Mode | Office-Based |
| Job Location | India |
| Positions | Site Solutions Executive; Site Solutions Executive Level 2 |
| Job Requisition IDs | R7194, R7191 |
| Job Posting | November 2026 |
| Application Mode | Online |
1. Site Solutions Executive – Mysore
Job Requisition ID: R7194
Location: Mysore, Karnataka, India
Premier Research is looking for a Site Solutions Executive / Clinical Research Coordinator to support one of its clinical research sites in Mysore.
Candidates must be proficient in reading and writing Kannada.
Key Responsibilities
- Coordinate and facilitate clinical trial activities at the site in compliance with study protocols, GCP guidelines and local regulations.
- Support the Principal Investigator and site study team in meeting sponsor and regulatory requirements.
- Perform timely data entry in Case Report Forms (CRFs) and Electronic Case Report Forms (eCRFs).
- Maintain clinical trial documentation, including the Trial Master File (TMF).
- Prepare for and support site initiation, monitoring and close-out visits, sponsor visits, QA visits and inspections.
- Report site performance metrics at predetermined intervals.
- Coordinate submissions of protocols, adverse events and periodic study reports to the Ethics Committee.
- Assist in scheduling patient investigations and assessments.
- Ensure the availability, storage and accountability of Investigational Products (IP), laboratory kits and other clinical trial supplies.
- Coordinate laboratory sample collection and reporting.
- Assist with data query resolution and protocol-related procedures.
- Support patient screening, enrolment, scheduling and study visits.
- Maintain communication with site monitors, investigators, sponsors and CRO representatives.
- Support patient-awareness activities, training events and site-level data collection.
- Develop databases of potential patients eligible for clinical trial enrolment.
- Identify operational challenges and coordinate mitigation plans with the relevant teams and Principal Investigator.
- Complete mandatory training, SOPs and ongoing training modules.
- Support audit and inspection readiness and help address audit findings.
Eligibility and Qualifications
- Bachelor’s or Master’s degree in clinical, biological or mathematical sciences or related fields.
- Medical or dental degree or nursing qualification.
- Candidates qualifying through the stated educational exceptions require 1–4 years of experience working at clinical research sites.
- Proficiency in reading and writing Kannada.
- Good oral and written communication skills in English and at least one local Indian language.
2. Site Solutions Executive Level 2
Job Requisition ID: R7191
Location: Regional India
Premier Research is hiring a Site Solutions Executive Level 2 for its India Operations team. The position focuses on coordinating clinical trial activities, supporting Principal Investigators and maintaining clinical research site processes and documentation.
Key Responsibilities
- Coordinate clinical trial activities at the site in accordance with protocols, GCP guidelines and local regulations.
- Support Principal Investigators and site study teams in meeting sponsor and regulatory requirements.
- Review site processes, identify operational gaps and support process implementation.
- Perform timely CRF and eCRF data entry in consultation with investigators.
- Maintain clinical trial documentation, including the Trial Master File.
- Prepare for and assist with site initiation, monitoring and close-out visits.
- Support patient visits, QA visits, sponsor visits and regulatory inspections.
- Report site performance metrics at predetermined intervals.
Eligibility and Qualifications
- Bachelor’s or Master’s degree in clinical, biological or mathematical sciences or related fields.
- Medical or dental degree or nursing qualification.
- Candidates qualifying through the stated educational exceptions require a minimum of 4 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 for Both Positions
Candidates should possess the following skills:
- Clinical trial coordination and site management.
- Good Clinical Practice (GCP) awareness.
- Clinical trial documentation and data accuracy.
- CRF and eCRF data entry.
- Trial Master File maintenance.
- Communication and interpersonal skills.
- Coordination and organizational abilities.
- Problem-solving and analytical skills.
- Attention to detail.
- Understanding of clinical research ethics, patient safety and patient rights.
- Familiarity with computers and office communication tools.
