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Clinical Research Associate Ii

Fortrea
2+ years
₹8–12 LPA
Bangalore, India
15 July 7, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Clinical Research Associate II (CRA II)

Location: Bangalore
Department: Clinical
Employment Type: Full-Time

Experience: Minimum 2+ years of independent Clinical Monitoring experience in clinical research, including site monitoring, GCP compliance, and study management.
Salary Package: ₹8–12 LPA (Approx., based on current market standards; final compensation depends on candidate experience, therapeutic area expertise, and skills.)


Role Overview

The Clinical Research Associate II (CRA II) is responsible for independently managing clinical trial sites, ensuring compliance with ICH-GCP guidelines, sponsor requirements, and regulatory standards. The role involves end-to-end site monitoring, data quality oversight, regulatory compliance, and maintaining audit readiness throughout the clinical trial lifecycle.


Key Responsibilities

Clinical Site Monitoring

  • Independently manage assigned clinical study sites throughout the study lifecycle.

  • Conduct Pre-Study, Site Initiation, Routine Monitoring, Process Monitoring, and Close-Out Visits.

  • Prepare and implement study-specific monitoring plans.

  • Verify study training records and ensure site readiness.

Regulatory & Compliance

  • Ensure compliance with ICH-GCP Guidelines, protocol requirements, sponsor SOPs, and local regulatory requirements.

  • Verify informed consent procedures and participant eligibility.

  • Maintain audit-ready study documentation and site files.

  • Ensure site regulatory documents and eTMF records remain complete and current.

Data Quality & Documentation

  • Perform Source Data Verification (SDV) and source document review.

  • Review electronic Case Report Forms (eCRFs), generate and resolve queries.

  • Ensure study data accuracy, completeness, consistency, and integrity.

  • Prepare and submit accurate monitoring visit and trip reports within required timelines.

Investigational Product (IP) Management

  • Verify investigational product inventory, storage, and accountability.

  • Track IP shipments and study supplies as required.

Safety Management

  • Track and follow up on Serious Adverse Events (SAEs).

  • Ensure timely reporting and documentation of safety events.

Project & Study Coordination

  • Collaborate with study teams to ensure project timelines and deliverables are achieved.

  • Participate in investigator meetings, project meetings, and study teleconferences.

  • Present training during Site Initiation Visits (SIVs).

  • Support investigator recruitment, site management, and clinical project administration.

  • Update and maintain CTMS, eClinical systems, and sponsor trial management tools.

Leadership & Team Support

  • Act as Lead CRA when assigned.

  • Mentor and support new team members through co-monitoring and training.

  • Contribute to process improvements and operational excellence.

  • Perform additional responsibilities assigned by management.


Educational Qualification

  • Bachelor's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or another allied health discipline.

  • Equivalent relevant clinical research experience may be considered.


Required Experience

  • Minimum 2 years of Clinical Monitoring experience.

  • Experience independently conducting monitoring visits across multiple clinical trial phases.

  • Strong understanding of ICH-GCP Guidelines and local regulatory requirements.

  • Experience with eClinical systems, CTMS, and electronic data capture (EDC) platforms.

  • Knowledge of Serious Adverse Event (SAE) reporting processes.


Technical Skills

  • Strong knowledge of Clinical Trial Monitoring procedures.

  • Experience with CTMS, eTMF, EDC, and other clinical electronic systems.

  • Proficiency in Microsoft Office Suite.

  • Understanding of clinical trial documentation and regulatory requirements.

  • Strong documentation, reporting, and data review skills.


Key Competencies

  • Strong organizational and project management skills.

  • Excellent analytical and problem-solving abilities.

  • High attention to detail and data accuracy.

  • Excellent communication and stakeholder management skills.

  • Ability to work independently with minimal supervision.

  • Strong interpersonal and collaboration skills.

  • Customer-focused approach with commitment to quality.

  • Ability to maintain confidentiality and regulatory compliance.

  • Effective planning, negotiation, and decision-making skills.

  • Adaptability in a matrix and fast-paced clinical research environment.


Travel Requirement

  • Travel: Approximately 60%, including regular travel to clinical study sites.

  • Ability to travel by air and work outside standard business hours when required.