Provide regional and global operational leadership across clinical trials, ensuring high-quality monitoring and site management throughout the study lifecycle.
Compensation
Annual salary ranging from $86,000 to $143,000, plus bonus.
Responsibilities
Provide regional and/or global clinical operations oversight across assigned clinical trials, ensuring compliance with study protocols, Monitoring Plans, ICH-GCP guidelines, applicable regulations, and project timelines.
Lead and support Clinical Operations Leads (COLs) and Clinical Research Associates (CRAs), providing study-specific guidance, training, mentoring, and operational direction throughout the clinical trial lifecycle.
Oversee monitoring and site management deliverables, including visit schedules and reports, recruitment progress, essential document collection, protocol deviations, and adherence to Monitoring Plans.
Lead and contribute to country and site feasibility assessments, selection, and start-up activities, providing operational input into country and site strategies.
Act as a key point of coordination between monitoring teams, Clinical Project Management, cross-functional stakeholders, and Sponsors, escalating operational risks and supporting the implementation of corrective actions.
Requirements
Bachelor's degree in a relevant discipline
Nice to have: Clinical Operations Lead experience
Wellness Nurse
Spectrum Retirement Communities, LLC · Posted Nov 12, 2026
The Wellness Nurse supports the health and well-being of residents through ongoing clinical monitoring and support, provides assistance to community nurses, caregivers, and medication personnel to help ensure regulatory compliance and clinical excellence.
Responsibilities
Assist in coordination of the resident admission process including screening, assessment, and care needs
Ensure care is delivered as indicated in resident care plans
Medication and treatment administration and ensure medications are administered per physicians’ orders
Assistance with coordinating care and services with other outside providers including resident physicians
Document and report care provided and resident observations including unusual or significant changes
Requirements
Graduate from an accredited school of practical nursing
Senior Clinical Research Associate (Level I) responsible for remote or on‑site monitoring of clinical trials, ensuring compliance with ICH‑GCP and sponsor protocols.
Responsibilities
Monitors investigator sites using risk‑based monitoring
Conducts on‑site and remote monitoring activities
Documents observations and escalates deficiencies
Provides trial status tracking and progress reports
Participates in investigator meetings
Requirements
Bachelor's degree in a life sciences related field
The Clinical Trial Manager is accountable for achieving the final clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the customer.
Responsibilities
Manage all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP
Develop clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan
Contribute to the development of the Master Action Plan (MAP) for providing clinical related documents
Ensure timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central)
Collaborate with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings
Requirements
Bachelor's degree or equivalent and relevant formal academic / vocational qualification
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
The Senior Clinical Research Associate (SCRA) is responsible for the initiation, monitoring, management, and close-out of study sites in accordance with protocol requirements, ICH-GCP guidelines, company SOPs, and applicable regulatory requirements.
Compensation
We provide a competitive compensation package, comprehensive benefits, and opportunities for professional growth within a collaborative and rewarding environment.
Responsibilities
Perform site qualification, initiation, routine monitoring, and close-out visits across assigned clinical trials
Ensure protocol compliance, data quality, patient safety, and regulatory adherence at investigative sites
Conduct remote and on-site monitoring activities, including source data verification and risk-based monitoring tasks
Build and maintain effective relationships with investigators, study coordinators, and site personnel
Identify, document, and escalate site issues while driving timely resolution and mitigation plans
Performs and coordinates all aspects of the clinical monitoring and site management process, conducting remote or on-site visits to assess protocol and regulatory compliance.
Responsibilities
Monitors investigator sites with a risk-based monitoring approach
Applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions
Ensures data accuracy through SDR, SDV and CRF review
Assess investigational product through physical inventory and records review
Documents observations in reports and letters
Requirements
Bachelor's degree in a life sciences related field
Sr. Clinical Operations LeadNewJobgether · US
Senior Clinical Research AssociateNewTFS HealthScience · Paris, France