Clinical QC Consultant

Position Overview Clinical QC Consultant – Job Description The Clinical QC Consultant is responsible for ensuring the quality, accuracy, and compliance of clinical trial documentation and data. This role supports clinical operations by performing quality control reviews and ensuring adherence to regulatory requirements and internal standards. Key Responsibilities Perform QC review of clinical documents, including: Clinical study reports (CSRs) Protocols and protocol amendments Informed consent forms (ICFs) Monitoring visit reports Trial master file (TMF) documents Ensure compliance with: Food and Drug Administration (FDA) regulations International Council for Harmonisation (ICH) guidelines Good Clinical Practice (GCP) standards Verify data accuracy and consistency across clinical systems (e.g., EDC, CTMS, TMF) Identify discrepancies, errors, or missing information and communicate findings to clinical teams Ensure proper documentation, version control, and audit readiness Support inspection readiness activities and participate in internal audits Collaborate with cross‑functional teams including Clinical Operations, Data Management, and Regulatory Affairs Assist in the preparation of protocols (including administrative letters for protocols and summary of changes for protocol amendments) and CSRs Assist in the preparation of study‑level documentation required for clinical trials (e.g., CSR appendices, shell drafts) Edit CSR statistical analysis plans and table/figure/listing specifications for grammar, format, and consistency Support authoring of protocols, investigator brochures, CSRs and other study‑level documentation required for clinical trials Edit submission documents (sections of CSRs, IND/CTA, NDA, MAA, requests for information and briefing documents) for regulatory agencies Review CSR statistical analysis plans and table/figure/listing specifications for grammar, format, and consistency Required Qualifications Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field 5+ years of experience in clinical research, QA/QC, or clinical operations Strong knowledge of FDA regulations, ICH guidelines, and GCP Experience reviewing clinical trial documentation and TMF management High attention to detail and strong analytical skills Preferred Qualifications Experience in hepatology or rare disease clinical trials (relevant to focus areas) Prior experience in a biotech or pharmaceutical company Familiarity with electronic systems such as Veeva Vault, Medidata, or similar Key Skills Quality control and audit readiness Documentation review and compliance Communication and collaboration Problem‑solving and critical thinking Work Environment Contract/consultant role Remote or hybrid (depending on project needs) May require collaboration across global teams #J-18808-Ljbffr MEDVACON LIFE SCIENCES, LLC