Clinical Trial Associate, Clinical Operations

Location
San Francisco, CA, United States
Posted
Sep 05, 2020
Ref
4860031002
Hotbed
Biotech Bay
Required Education
Bachelors Degree
Position Type
Full time
Nurix was founded by internationally recognized experts in the ubiquitin-proteasome (UPS) field and received its initial funding from leading life science investors Third Rock Ventures and The Column Group. Nurix recently entered into a multi-year collaboration with Gilead and Sanofi focused on developing bi-functional molecules to degrade protein targets as novel therapeutics. Additionally, Nurix has a strong internal drug discovery pipeline focused on oncology, immunology and inflammation. Nurix plans to advance two molecules into clinical trials in early 2021.

Position

The Clinical Trial Associate supports Clinical Operations by performing a variety of administrative and operational activities associated with all phases of clinical trials.

Required Qualifications
  • Bachelor's degree (BS/BA) or equivalent combination of education and work experience in science related field
  • Clinical Operations or clinical research-related experience is desired (1-2 years)
  • Familiarity with document filing/management in an electronic Trial Master File preferred
  • Strong attention to detail in composing and proofing materials, establishing priorities, scheduling, and meeting deadlines
  • Excellent verbal and written communication skills
  • Proficiency with MS Word, Excel, Outlook, and PowerPoint

Responsibilities:
  • Assist in the development, review, and formatting of study-specific documents, including plans, manuals, CRFs, patient documents, reference documents, and study tools
  • Develop study-specific TMF plan(s) and manage/oversee collecting, tracking, and archiving of Essential Documents throughout the life of the study
  • Conduct quality reviews of the TMF and work with CRO to resolve discrepancies
  • Assist in the coordination and tracking of clinical supplies and laboratory samples
  • Participate in the review of clinical data in the clinical database, data listings, and reports
  • Assist with data reconciliation of various systems, as required
  • Coordinate preparation of study-specific training materials, as required
  • Maintain and update study trackers/metrics on an on-going basis
  • Facilitate the preparation of meeting agendas and take meeting minutes for clinical team meetings
  • Attend Investigator Meetings and/or support meeting planning
  • Complete additional tasks as assigned and agreed upon

Fit with Nurix Culture and Values
  • Strong team orientation; highly collaborative
  • Solutions and results-oriented focus
  • Hands-on approach; resourceful and open to diverse points of view


Application Process

Nurix is an Equal Opportunity Employer offering a competitive salary and benefits package. Applicants should be legally entitled to work for any employer in the US.

Note to Employment Agencies: Please do not forward any agency resumes. Nurix will not be responsible for fees related to unsolicited resumes.