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Lead Researcher - Compliance Monitoring Team

5-10 years
Not Disclosed
10 Aug. 1, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, 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 Opening: Lead Researcher - Compliance Monitoring Team

Location: Arcolab, Bangalore

Experience Level: 5 to 10 years

Job Description:

Arcolab is seeking a Lead Researcher with extensive experience in compliance monitoring for clinical trials, bioavailability/bioequivalence (BA/BE) studies, and pharmacovigilance. The ideal candidate will play a crucial role in ensuring quality and regulatory compliance across various operations.

Key Responsibilities:

  • Quality Management System: Assist in establishing and maintaining the quality management system for clinical trials, BA/BE studies, and pharmacovigilance activities.

  • Compliance Monitoring: Oversee compliance monitoring to ensure adherence to regulatory guidelines and internal standards within clinical trials and BA/BE organizations.

  • Process Improvement: Identify and implement process improvements and optimization strategies in pharmacovigilance (PV) and clinical operations (CO).

  • Regulatory Support: Provide support to the Medical Affairs team in interpreting and applying regulatory guidelines.

  • Trend Analysis: Track and analyze compliance review trends in PV and CO to identify areas for improvement.

  • SOP Development: Assist in the preparation and review of standard operating procedures (SOPs) for clinical trials, BA/BE studies, and PV.

  • Data Review: Conduct reviews of clinical trial data throughout its lifecycle, including paper-based and electronic systems.

  • Quality Control: Perform quality control reviews of key trial documents such as protocols, informed consent forms, clinical study reports, and investigator brochures.

  • Pharmacovigilance Oversight: Oversee quality control processes for PV activities, including individual case safety reports (ICSR), aggregate reports, and signal detection.

  • Audit Preparation: Participate in internal and external audit preparations, inspections, and ensure audit readiness.

  • Risk Management: Manage risks related to CO and PV functions, implementing risk mitigation strategies as needed.

  • ISO Compliance: Support the implementation and adherence to ISO 27001 and ISO 27701 standards, ensuring data security and privacy compliance.

Application Process:

Interested candidates are invited to share their resumes with Dev Kiran at dev.kiran@arcolab.com.