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Cra (Level I, Level Ii And Sr Cra)

2+ years
Not Disclosed
10 Sept. 25, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title:

Clinical Research Associate (CRA) – Level I, Level II, Senior CRA

Location:

Remote, India (Fully Onsite when required)

Job ID:

R-01326248

Job Type:

Full-time

Category:

Clinical Research / Monitoring

Work Schedule:

Standard (Mon-Fri)

Work Environment:

  • Office and on-site monitoring environments

  • May include non-traditional work settings

  • Exposure to clinical or laboratory environments

  • Independent travel up to XX% (cars, airplanes, trains)

  • Able to communicate with diverse groups effectively

  • Able to perform under pressure and manage multiple projects simultaneously


About the Role:

The CRA performs and coordinates all aspects of clinical monitoring and site management, ensuring trials are conducted according to protocol, ICH-GCP, regulatory requirements, and SOPs. The role involves remote and on-site visits, site process management, data verification, and collaboration with investigational sites to guarantee subject safety and data integrity.


Key Responsibilities:

Clinical Monitoring & Site Management:

  • Conduct remote or on-site site visits to ensure protocol compliance.

  • Manage procedures and guidelines from different sponsors and monitoring environments (FSO, FSP, Government).

  • Ensure audit readiness and proper documentation of all monitoring activities.

  • Develop collaborative relationships with investigational sites.

  • Apply risk-based monitoring, root cause analysis, and corrective/preventive actions to address site issues.

  • Ensure data accuracy via SDV, SDR, and CRF review.

  • Assess investigational products through physical inventory and records review.

  • Escalate observed deficiencies to clinical management and track resolution.

  • Maintain regular site communication to ensure adherence to protocols.

Project & Documentation Support:

  • Conduct trial close-out and retrieval of trial materials.

  • Ensure essential documents are complete per ICH-GCP and regulations.

  • Conduct on-site file reviews per project specifications.

  • Update study systems per agreed conventions (e.g., CTMS).

  • Facilitate communication between investigative sites, clients, and project teams.

  • Maintain administrative tasks such as timesheets and expense reports.

  • Contribute to project publications, tools, and process improvement initiatives.


Qualifications & Experience:

Education:

  • Bachelor’s degree in life sciences or related field, OR

  • Registered Nursing certification or equivalent formal academic/vocational qualification.

Experience:

  • Minimum 2+ years as an onsite clinical research monitor (experience may vary by CRA level).

  • Valid driver’s license where applicable.

  • Equivalent combination of education, training, and related experience may be considered.

Knowledge, Skills & Abilities:

  • Proven clinical monitoring skills and medical/therapeutic knowledge.

  • Understanding of ICH-GCP, regulatory requirements, and procedural documents.

  • Critical thinking, root cause analysis, and problem-solving skills.

  • Risk-based monitoring expertise.

  • Strong oral and written communication skills.

  • Customer-focused with good listening and attention to detail.

  • Organizational and time management skills.

  • Interpersonal skills and ability to work independently or in a team.

  • Proficient in Microsoft Office and ability to learn software.

  • Presentation skills and strong command of English.