About the role

  • Clinical Research Associate managing clinical trials for Summit Therapeutics. Supporting complex global studies while ensuring adherence to metrics and quality deliverables from study planning to close out.

Responsibilities

  • Supports all aspects of Clinical Trial Management for complex, global studies
  • Collaborates with functional team members, CROs, and vendors
  • Directs and completes communication between the project team and site personnel
  • Reviews, approves, and tracks vendor invoices and manages accruals and payment process for all assigned clinical trial vendors
  • Initiates and builds professional relationships with clinical site staff
  • Responsible for the development and management of clinical trial documents
  • Provides close oversight on findings on the monitoring reports

Requirements

  • Bachelor's degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or related field preferred
  • 3+ years of clinical research experience in conducting clinical trials
  • Prior phase II or III experience required
  • Sophisticated understanding and highly skilled utilization of Microsoft Apps such as Outlook, Word, Excel, and Teams
  • Ability to travel internationally to visit clinical sites and for study meetings (up to 20%)
  • Excellent interpersonal and decision-making skills
  • Experience in working in a small organization a plus
  • Excellent written and oral communication skills.

Benefits

  • Bonuses
  • Stock options
  • Health insurance
  • Flexible work arrangements
  • Professional development opportunities

Job title

Clinical Research Associate

Job type

Experience level

JuniorMid level

Salary

$97,000 - $114,000 per year

Degree requirement

Bachelor's Degree

Location requirements

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