Contract - Senior Clinical Trial Assistant

San Francisco, CA, United States
Jun 16, 2021
Biotech Bay
Required Education
Bachelors Degree
Position Type
Full time

Position Summary:

The Senior Clinical Trial Assistant (CTA) is responsible for providing support to the lead Clinical Trial Manager (CTM) and Clinical Research Associate (CRA) in the management of clinical trials.

The Sr. CTA will be responsible for tracking and document maintenance as applicable and supporting the oversight of vendors and clinical trial sites. The Sr. CTA will work closely with a cross-functional team to ensure that clinical trials are conducted in a timely fashion and in compliance with GBT SOPs, ICH/GCP/regulatory guidelines, company goals and budgets.

Essential Duties and Responsibilities:
  • Support one or more study execution team (SETs), including scheduling meetings, distributing agendas and meeting minutes
  • Document outstanding action items with expected completion dates and responsible individual(s). Follows-up on all SET action items
  • Support SET risk management discussions, follow-up and documentation
  • Track and maintain study information and report on study progress
  • Track and provide IRB/IEC submission documentation and other supplementary documentation, as appropriate
  • Obtain, review, process, and track study related documents (CVs, FDA 1572s, lab certifications, IRB approvals, contracts, protocols, etc.)
  • Maintain and disseminate basic study tracking information including, but not limited to: visit reports, regulatory documents, site contact lists, team contact lists and vendor lists
  • Lead Essential Document Packet review and approval process
  • Lead ICF development, review and approval process
  • Attend monitoring oversight visits with CRA or CTM​, where needed and as appropriate
  • Maintain and ensure the completeness of the Trial Master File (TMF) in accordance with SOP requirements
  • In collaboration with Supply chain, lead the management and tracking Investigational Product (IP)supplies for study sites
  • Oversight of preparation, shipment and management of study supplies to sites
  • Support preparation of materials for investigator meetings, workshops, and study manuals
  • Lead development of study newsletters
  • Lead onboarding of new CTA team members
  • Identify and support process improvement initiatives
  • All work must adhere to ICH Good Clinical Practice (GCP) guidelines and comply with company SOPs

  • Bachelor's degree or equivalent or combination of relevant experience and training
  • 2 to 4 years of relevant industry experience
  • Effective communication skills
  • Excellent organizational skills and attention to detail
  • Excellent problem-solving skills
  • Ability to efficiently perform multiple tasks and manage changing priorities
  • Appropriate and timely escalation
  • Ability to complete activities with minimal oversight
  • Demonstrate proficiency in Microsoft Word, PowerPoint and Excel
  • Take direction well