Serves as the primary site manager for assigned clinical investigative sites
Is the frontline liaison between Novartis and sites to ensure successful collaboration
Manages assigned study sites/networks, conducting phase I-IV protocols according to the monitoring plan and Novartis procedures
Facilitates the preparation and collection of site and country level documents
Performs Site Initiation Visit, ensures site personnel are fully trained on all trial-related aspects
Conducts continuous monitoring activities (onsite and/or remote)
Accountable for continuously updating all relevant electronic systems to perform job functions
Monitors studies as per current legislations, ICH/GCP and Novartis standards
Ensures timely delivery, of high quality, robust and reliable data of the monitored sites
Collaborates with internal stakeholders and site personnel to manage data query resolution process

BS/BA degree. Scientific, Healthcare or other related field.
Excellent knowledge of the drug development process specifically clinical trial/research
Knowledge of international standards (GCP/ICH, FDA, EMEA)
Ability to manage multiple priorities and manage time efficiently.
Excellent Site management capabilities with demonstrated negotiating and problem-solving skills
Strong communicator and presentation skills (oral and written)
Fluent in both written and spoken English.
Minimum of 3 years of experience in site monitoring strongly preferred
RLT, CAR T or Oncology experience a plus!

Health insurance
Life and disability benefits
401(k) with company contribution and match
Generous time off package including vacation, personal days, holidays and other leaves
Performance-based cash incentive
Eligibility for annual equity awards

Senior Clinical Research Associate

Key skills