Lead end-to-end data management activities across clinical studies and development programs, ensuring clinical data is accurate, complete, reliable, and inspection-ready throughout the study lifecycle.
Compensation
Anticipated annual salary range of $145,000–$160,000, depending on experience, qualifications, internal equity, and location.
Annual bonus eligibility.
Significant equity opportunities.
Responsibilities
Oversee clinical data management strategy and execution for assigned studies
Serve as the lead Clinical Data Manager and primary Data Management contact for assigned studies
Lead core data management processes, including EDC database development, eCRF design, edit check specifications, user acceptance testing, Data Management Plans, database changes, data cleaning, external data reconciliation, and database lock activities
Oversee Data Management deliverables across assigned programs and provide expert guidance on the setup, configuration review, and user acceptance testing of Randomization and Trial Supply Management (RTSM) systems
Translate clinical protocol requirements into fit-for-purpose electronic Case Report Forms (eCRFs), data collection processes, and study-specific data review tools
Requirements
Bachelor's degree
Nice to have: Scientific or healthcare-related degree
Perform and coordinate all aspects of the clinical monitoring and site management process as a Clinical Research Associate (Level II), conducting remote or on-site visits to assess protocol and regulatory compliance.
Compensation
The salary range estimated for this position based in Illinois is $66,800.00–$125,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.
Responsibilities
Monitors investigator sites with a risk-based monitoring approach
Ensures data accuracy through SDR, SDV and CRF review
Assess investigational product through physical inventory and records review
Escalates observed deficiencies and issues to clinical management expeditiously
Conducts monitoring tasks in accordance with the approved monitoring plan
Requirements
Bachelor's degree in a life sciences related field
Play a key role in moving clinical trials forward by supporting the development, negotiation, and finalization of site agreements, amendments, budgets, and other site-related contractual documents.
Responsibilities
Prepare, draft, negotiate, and finalize site agreements, amendments, budgets, and other site-related contractual documents.
Negotiate contract language and study budgets with assigned clinical research sites through execution.
Review agreements and supporting documents for completeness, accuracy, quality, and compliance before signature.
Identify and escalate contractual risks, requests outside approved parameters, and non-responsive sites to the appropriate study stakeholders.
Collaborate with Legal, Data Privacy, study teams, sponsors, sites, and investigators to resolve contract-related questions and issues.
Requirements
Bachelor’s degree or equivalent in business administration, finance, science, or a related field
Contribute to clinical trial operations by delivering clinical trial monitoring work to a high standard, working collaboratively to deliver high-quality outcomes across clinical programmes.
Compensation
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Responsibilities
Coordinate all activities for setting up and monitoring a study
Complete accurate study status reports and maintain study documentation
Run sponsor generated queries efficiently and take responsibility for study cost efficiency
Participate in the preparation and review of study documentation and feasibility studies for new proposals
Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff
Requirements
University degree in medicine, science, or equivalent
Perform and coordinate different aspects of the clinical monitoring and site management process as a Clinical Research Associate I, conducting remote or on-site visits to assess protocol and regulatory compliance.
Responsibilities
Monitors investigator sites with a risk-based monitoring approach
Ensures data accuracy through SDR, SDV and CRF review
Documents observations in reports and letters
Escalates observed deficiencies and issues to clinical management
Maintains regular contact between monitoring visits with investigative sites
Requirements
Bachelor's degree in a life sciences related field
Senior Manager, Data ManagementNewJobgether · New York City, US