Chief Compliance Officer

2 days ago

Davangere, Karnataka, India beBeeClinicalCompliance Full time ₹ 19,99,950 - ₹ 24,99,900
Job Title: Clinical Quality Assurance Compliance & Training

Experience: 5 plus years.

Location: Mumbai.

Type: Full-time.

Experience Level: Senior Manager/Senior Manager.

Department: Clinical Research Department

This role will be responsible for oversight on end-to-end clinical trial activities from a quality perspective. The candidate will be accountable for quality compliance (QC) activities of the clinical trial medical science team and operations team, clinical trial supply management (CTSM) team, and clinical data management team by reviewing all study-related activities, processes, procedures, and adherence to applicable regulations and guidelines to ensure 24x7 inspection/audit readiness.

The successful candidate will be responsible for establishing procedures and trainings of teams that ensure protection of human subjects from research risk, reliability/integrity of the data, and thereby assures internal consistency and quality compliance measures.

They will develop and implement a risk-based and flexible approach to quality compliance (QC) within the function, which will ensure that trial participants and data are safeguarded in compliance with applicable regulatory requirements and best practices.

  • Identify and decide team member's job-specific SOP training requirements in view of their role and maintain oversight of training to ensure all team members are trained on each SOP as required.
  • Preparation of SOPs related to QC function and support in review of SOPs specific to Medical science, Clinical team, and Data Management team.
  • Quality review of the clinical trial medical science related activities like synopsis, protocol, clinical study report (CSR), and appendices, and SOPs in line with ICH GCP requirement, Indian and global regulatory requirement.
  • Quality review of the clinical trial operation related activities, related tools, plans, and documentation like site feasibility, site selection visit, site initiation, Ethic committee documentation, monitoring – site-specific reports, Site Documents, logs, and close-out activities in line with ICH GCP requirement, Indian and global regulatory requirement.

Key Requirements:

  • 5 years' experience in a CRO/Pharma/Biotech organization in the quality department with experience of quality activities in the clinical research department.
  • Strong eye for detail and ability to spot inconsistencies is a must, along with good conflict management skills.
  • Must have experience in handling audits & inspections of DCGI, US FDA.
  • Thorough knowledge of recent GCP guidelines, ICMR guidelines, Drugs and Cosmetic Act regulations, and other applicable regulations pertaining to clinical trials.
  • Experience of working in matrix business environments is preferred.
  • Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.

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