Clinical Research Associate (CRA I/II) roles continue to be among the most in-demand positions in the clinical research industry. A leading global clinical research organization, Clinical Research Group (CRG), is hiring CRA Level I and II professionals for a full-time, fully remote role based in Mumbai, India.
This opportunity is ideal for candidates with 1โ1.5 years of on-site monitoring experience who want to work on global clinical trials, collaborate with top pharmaceutical and biotech sponsors, and advance their careers in risk-based monitoring and ICH-GCPโcompliant studies.
Key Responsibilities โ CRA I / CRA II Job
As a Clinical Research Associate, you will be responsible for end-to-end monitoring activities, ensuring protocol compliance and data integrity.
- Coordinate and oversee clinical trial activities from site start-up to close-out
- Conduct on-site and remote monitoring visits as per monitoring plans
- Perform risk-based monitoring (RBQM), including SDV and SDR
- Review clinical trial data on EDC, CTMS, IWRS, and eTMF systems
- Ensure trials comply with ICH-GCP, SOPs, and regulatory requirements
- Maintain audit readiness and support site audits and inspections
- Prepare and submit accurate monitoring visit reports and follow-up letters
- Track country-level metrics and resolve site issues proactively
- Communicate regularly with investigators and site staff
- Support CAPA development and implementation
- Mentor and support junior CRA team members when required
- Travel to sites as per monitoring plan (up to 60โ75% travel)
- Complete administrative tasks including timesheets and expense reports
Eligibility Criteria & Qualifications
To be considered for this CRA I/II position, candidates must meet the following requirements:
- Postgraduate degree in Life Sciences or related discipline
- Minimum 1โ1.5 years of on-site monitoring experience (mandatory)
- Strong working knowledge of ICH-GCP and regulatory guidelines
- Experience in FSP model is preferred but not mandatory
- Proficiency in clinical systems such as CTMS, EDC, IWRS, eTMF
- Valid driverโs license (where applicable)
- Excellent written and verbal English communication skills
Required Skills & Competencies
- Strong client and stakeholder management abilities
- High attention to detail and documentation accuracy
- Ability to manage multiple clinical trials simultaneously
- Problem-solving and risk mitigation skills
- Independent working capability with strong team collaboration
- Digital literacy with Microsoft Office and clinical trial software
Why Join CRG?
- Work on global clinical trials across 100+ countries
- Exposure to top 50 pharmaceutical companies and 750+ biotechs
- Fully remote work model with structured support
- Career progression from CRA I to CRA II and beyond
- Continuous learning, training, and mentoring opportunities
- Strong focus on quality, compliance, and innovation
Salary & Compensation
- Estimated Salary Range: โน6,00,000 โ โน12,00,000 per annum (CTC)
- Salary will be commensurate with experience, level (CRA I or CRA II), and project complexity
How to Apply
