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Clinical Trial Coordinator
Confirmed live in the last 24 hours
Locations
Fremont, CA, USA
Experience Level
Entry
Junior
Mid
Senior
Expert
Desired Skills
Management
Research
Requirements
  • Working knowledge of medical and scientific terminology
  • Demonstrated communication and management skills
  • Demonstrated problem-solving abilities and demonstrated tactfulness and diplomacy in communication, preferably in a medical setting
  • Basic understanding of the clinical trial process
  • Experience working collaboratively and effectively on a team
  • Self driven; able to initiate and work independently
  • Effective communicator; able to present information to colleagues and lay audiences
  • Positive attitude: ability to work well with others
  • Adaptable to change and willing to accept added responsibilities and accountability
  • Ability to meet deadlines with accuracy and efficiency
  • Great attention to detail and organizational skills
  • Effective multitasking skills
  • Ability to work in a dynamic environment and effectively and collaboratively in a cross-disciplinary team
Responsibilities
  • Support Neuralink clinical studies by ensuring adherence to study protocols as well as ensuring compliance with regulations and standards for clinical research
  • Serve as the first line of contact with interested clinical trial participants
  • Establish and maintain relationships with community partners and patient advocacy groups
  • Assist Community Engagement team with trial recruitment activities
  • Review study specific materials and extract relevant data
  • Develop and implement SOPs for clinical trials and related activities
  • Collect and complete regulatory documents for the Sponsor and Institutional Review Board (IRB) as needed
  • Provide regulatory assistance when needed including, but not limited to safety reports, SAE reporting, additional submissions, approvals, and closures
  • Support Clinical Research Associate(s) to conduct study monitoring visits and prepare for site audits
  • Maintain a working knowledge of and assure compliance with Good Clinical Practices, Federal Regulatory requirements, Risk-Based Approach to Monitoring, and Neuralink SOPs
Desired Qualifications
  • Experience with clinical studies
  • Basic knowledge of Good Clinical Practice (ISO 14155), 21 CFR part 50, 54, 56, 812 and other applicable regulations
  • Experience coordinating clinical trials or research
Neuralink

51-200 employees

Implantable brain–machine interfaces
Company Overview
Neuralink's mission is to build devices that will help people with paralysis and invent new technologies that will expand abilities, the community, and the world.
Benefits
  • An opportunity to change the world and work with some of the smartest and the most talented experts from different fields.
  • Growth potential. We rapidly advance team members who have an outsized impact.
  • Excellent medical, dental, and vision insurance through a PPO plan; parental leave.
  • Flexible time off + paid holidays.
  • Equity + 401(k) plan.
  • Commuter Benefits.
  • Meals provided.