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2-4 years
3.5 – 6 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: Senior Clinical Research Associate (Sr. CRA)
Location: Mohali/Chandigarh
Vacancy: 01

Job Overview:
We are seeking an experienced Senior Clinical Research Associate (Sr. CRA) to join our team. The ideal candidate will be responsible for performing various activities at clinical trial sites, ensuring adherence to protocol requirements and maintaining compliance with regulatory standards. This position offers an excellent opportunity for professionals with clinical research and onsite experience to contribute to the successful execution of clinical trials.

Key Responsibilities:

  • Perform various activities at clinical trial sites, ensuring compliance with study protocols, regulatory requirements, and standard operating procedures (SOPs).
  • Monitor and support the site staff to ensure the efficient conduct of clinical trials.
  • Conduct site initiation, monitoring, and close-out visits.
  • Ensure accurate and timely data collection, source document verification, and reporting of adverse events.
  • Collaborate with clinical trial teams to ensure proper handling of investigational products and documentation.
  • Provide training and guidance to site personnel on study procedures, safety requirements, and data integrity.
  • Review and verify clinical trial documentation, including case report forms (CRFs), informed consent forms (ICFs), and regulatory submissions.
  • Ensure the safety and well-being of study participants by adhering to ethical standards and GCP guidelines.

Qualifications:

  • 2-4 years of clinical research experience and hands-on onsite monitoring.
  • Strong understanding of clinical trial processes, regulatory guidelines, and GCP compliance.
  • Experience with clinical trial protocols and documentation.
  • Excellent communication, organizational, and problem-solving skills.
  • Ability to travel to clinical trial sites as required.

Compensation:

  • Annual Salary: ₹3,50,000 - ₹6,00,000

Skills & Competencies:

  • In-depth knowledge of clinical research processes and regulatory requirements.
  • Strong attention to detail and ability to maintain accurate documentation.
  • Effective communication skills and the ability to work collaboratively in a team environment.
  • Time management skills to handle multiple tasks efficiently.

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