Adela is focused on the detection of cancer and other high-morbidity, high-mortality conditions through a blood test. The Company’s genome-wide methylation analysis technology has the unique ability to   the most highly informative (methylated) regions of the genome from the non-informative regions and preferentially target those informative regions for sequencing. The technology is initially being developed for use across the cancer continuum for detection, diagnosis and management and in the future will be applied to other conditions beyond cancer. 

Summary:

Under the direction of the Associate Director of Clinical Operations and the Clinical Trial Manager, the Senior Clinical Research Associate contributes to the tactical implementation and conduct of clinical research studies. The Sr. CRA ensures the quality of each research study through on-site centralized, and remote monitoring of protocol and regulatory compliance. The SR. CRA represents Adela at the research site level and maintains collaborative relationships with investigator sites, any potential contract research organizations (CROs), and the internal clinical development team and may be responsible for junior level staff.

Responsibilities:

  • Serves as liaison between Adela clinical development team and research site staff with respect to tactical elements of study completion 
  • Assesses site qualification potential (reviews study requirements and identifies sites through feasibility and qualification visits) 

  • Completes study start-up activities: 

  • Assists with creation of study tools and training materials 

  • Directs site staff through start-up activities  

  • Assists with regulatory processes as needed 

    • Conducts on-site initiation, interim monitoring, and close-out visits per Adela SOP to ensure data integrity and good clinical practice; writes and submits visit reports 
    • Conducts centralized monitoring tasks (remote data review for identification of queries, data trends, deviations, issue escalation, etc.) 
    • Verifies and fulfills site supply requests for product/study materials 
    • Tracks and escalates any safety events 
    • Drafts CAPA/intervention plans 
    • Communicates site enrollment and study metrics through maintenance of tracking tools 
    • Maintains trial master files for assigned clinical research projects 
    • Maintains professional expertise through familiarity with up-to-date medical and clinical operations knowledge and familiarity with Adela’s product pipeline. 
    • Works independently with minimal instruction and routine supervision by CTM, or functional manager; may perform as CRA lead on studies as appointed by CRA Manager 
    • Ability to help train and supervise junior level staff  
    • Field site travel up to 30% 


    Requirements:

    • Knowledge of medical terminology, clinical monitoring procedures (SOPs), and ICH/GCP guidelines 
    • Proven ability for attention to detail and accuracy in work 
    • Excellent written and oral communication skills 
    • Excellent organizational and time management skills 
    • Strong computer skills including Microsoft Office, EDC systems, eTMF 




    This position has been filled.