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Director, Clinical Quality Assurance

10+ years
Not Disclosed
10 Dec. 11, 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, 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 Quality Assurance (CQA) Lead
Location: Remote (Global)
Employment Type: Full-time
Posted: 12/11/2024

About Biorasi:

At Biorasi, we are growing and looking to support your career journey in an innovative, collaborative, dynamic, and evolving environment. We capitalize on your strengths while encouraging work-life balance. As an award-winning, customer-focused, full-service clinical research organization, we thrive in a fast-paced environment, helping to drive new therapies to patients. Now’s your chance to be part of a growing global company in the expanding clinical research industry.

Your Role:

As CQA Lead, you will oversee Biorasi's compliance with national and international laws and regulations, including Good Clinical Practices (GCP). This position will involve the development and management of quality assurance (QA) processes and will be critical in ensuring compliance across the organization. Your key responsibilities include:

  • Leadership: Lead the Clinical Quality Assurance (CQA) function, developing strategies, policies, procedures, and tools for managing CQA processes and employees.
  • Consultation: Provide regulatory consultation to Biorasi teams and staff to interpret guidelines and regulations.
  • Regulatory Oversight: Ensure Biorasi SOPs and procedures comply with applicable regulations, including GCPs, and represent the company during regulatory inspections.
  • Audit & Quality Control: Develop and execute internal audit plans, corrective/preventive actions (CAPAs), and ongoing oversight to detect and mitigate risks or deviations.
  • Training & Development: Lead the development and delivery of training on regulations and best practices in collaboration with HR, Learning, and Development.
  • Resource Planning: Oversee CQA resource allocation and project budgeting, working closely with the project management and finance teams.
  • Quality Improvement: Champion Biorasi-wide quality improvement initiatives and collaborate with cross-functional teams on process implementation.
  • External Representation: Represent Biorasi at sponsor meetings, public speaking events, and other external engagements.

Your Profile:

  • Education: Degree in science, related scientific discipline, or business (Master’s degree preferred).
  • Experience: 10+ years in drug development or clinical research, with at least 3 years in quality assurance or quality management.
  • Skills:
    • Proven leadership ability with experience managing and developing teams.
    • Strong organizational, multitasking, and attention to detail skills.
    • Knowledge of ICH GCP and global regulatory requirements.
    • Excellent verbal, written communication, and presentation skills.
    • Ability to travel up to 25% of the time.

Why Biorasi?

  • Employee Benefits: Half-day Fridays, paid time off, paid holidays, employee bonus programs, career growth, and training opportunities.
  • Diversity and Inclusion: Biorasi is committed to creating a diverse and inclusive environment and is an equal opportunity employer.

Apply Now:

If you're ready to lead quality assurance at an innovative and collaborative company, apply directly on our website at Biorasi Careers or email us at careers@biorasi.com.