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1-2 years
3 -5 lacs per annum
10 Jan. 23, 2025
Job Description
Job Type: Full Time Education: B.Sc,M.Sc,B.Pharma,M.Pharma,LifeScience Graduates 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)
Location: Mohali/Chandigarh
Vacancy: 02

Job Overview:
We are looking for a Clinical Research Associate (CRA) with 1-2 years of relevant experience to join our team. The CRA will be responsible for carrying out various activities at clinical trial (CT) sites, ensuring compliance with the study protocol, regulatory guidelines, and Good Clinical Practice (GCP) standards.

Key Responsibilities:

  • Conduct site activities for clinical trials in accordance with study protocol and regulatory requirements.
  • Perform site monitoring visits to ensure compliance with study protocols, GCP, and SOPs.
  • Verify data accuracy, completeness, and integrity through source document verification and case report form (CRF) review.
  • Report and manage adverse events in compliance with regulatory guidelines.
  • Provide training and guidance to site personnel on clinical trial processes and requirements.
  • Ensure proper handling, storage, and accountability of investigational products at the site.
  • Ensure that informed consent forms (ICFs) are properly completed and documented.
  • Assist in site recruitment and retention efforts, ensuring participant safety and protocol adherence.
  • Communicate effectively with the clinical trial team and site staff to resolve issues and ensure trial success.

Qualifications:

  • 1-2 years of relevant experience in clinical research or clinical trials.
  • Knowledge of clinical trial processes, GCP, and regulatory guidelines.
  • Ability to ensure data accuracy and manage clinical trial documentation.
  • Strong organizational and communication skills.
  • Willingness to travel to clinical trial sites as needed.

Compensation:

  • Annual Salary: ₹3,00,000 - ₹5,00,000

Skills & Competencies:

  • Excellent attention to detail and ability to maintain high-quality data.
  • Strong problem-solving skills and ability to manage multiple tasks.
  • Effective communication skills to interact with study teams and site staff.
  • Proficiency with clinical trial documentation and clinical trial management systems (CTMS).

How to Apply:
Interested candidates are encouraged to apply by submitting their updated resume and relevant experience details on hr@indivirtus.com with CC to admin1@indivirtus.com