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The provider will deliver medication abortion and reproductive healthcare services via a virtual platform, including patient intake review and treatment planning. They are responsible for conducting video or phone appointments and coordinating with nursing staff for follow-up care and prescriptions.
The Initiation Clinical Research Associate leads and executes all study start-up, pre-SIV, activation, and protocol amendment activities. They act as the primary contact for assigned sites, managing regulatory submissions and ensuring compliance with sponsor and regulatory requirements.
You will provide strategic medical leadership and scientific guidance across project teams to ensure high-quality medical affairs delivery. Additionally, you will oversee compliance with regulatory standards and represent the department in business development initiatives.
The Clinical Trial Coordinator II provides administrative and technical support to the project team, ensuring audit readiness and efficient site activation. They are responsible for reviewing trial files, maintaining study metrics, and coordinating activities to meet project deadlines.
The Case Manager will assess client needs, coordinate services, and provide ongoing support to help clients achieve their goals. This role involves managing multiple cases while maintaining a client-centered approach and ensuring professional communication.
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The Clinical Research Associate conducts site monitoring visits to ensure clinical trial protocol compliance, data integrity, and adherence to regulatory standards. They provide leadership and guidance to site teams while managing study documentation, budgets, and cross-functional communication.
The Clinical Research Associate conducts site monitoring visits to ensure clinical trial protocol compliance, data integrity, and adherence to regulatory standards. They provide leadership and guidance to site staff while managing study documentation, budgets, and cross-functional communication.
The Clinical Research Associate conducts site monitoring visits to ensure clinical trial protocol compliance, data integrity, and adherence to GCP guidelines. They provide leadership and oversight to site teams while managing study budgets, regulatory documentation, and cross-functional communication.
The Clinical Research Associate conducts site monitoring visits and provides leadership to ensure clinical trials adhere to protocol, SOPs, and regulatory requirements. They manage site relationships, perform data verification, and collaborate with cross-functional teams to resolve study-related issues.
The Manager of Clinical Operations is responsible for overseeing the planning and execution of clinical trials to ensure compliance with protocols and regulatory standards. They will also mentor junior staff, manage cross-functional relationships, and drive continuous improvement in operational performance.
Manage pre-admission and prior authorizations with insurance providers while conducting concurrent reviews and clinical chart audits. Coordinate with clinical teams and maintain accurate authorization records in the electronic health record system.
Provide medical oversight for clinical trials, ensuring adherence to regulatory requirements and company SOPs. Conduct medical review and analysis of safety data, including serious adverse events and periodic safety reports.
The role involves managing patient inquiries, conducting intake screenings, and coordinating appointments for a behavioral health clinic. You will also maintain accurate documentation in the EHR and assist patients with portal navigation and paperwork.
Provide virtual clinical and administrative support to neurology clinics, including patient scheduling, intake, and documentation. Maintain accurate patient records in EHR systems while ensuring compliance with HIPAA regulations.
The Medical Review Officer interprets and reports drug test results for DOT and non-DOT clients while ensuring compliance with federal regulations. They also conduct interviews with donors to determine legitimate medical explanations for non-negative test results.
The Senior Medical Coding Specialist leads the medical coding process for clinical trial data, ensuring accuracy and compliance with industry standards. They also collaborate with cross-functional teams to resolve coding discrepancies and provide mentorship to junior staff.
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The Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining data integrity throughout clinical trials. They also collaborate with investigators and site staff to facilitate study conduct and contribute to the preparation of study documentation.
You will lead clinical research tasks, including the creation and maintenance of data management plans and documentation to ensure regulatory compliance. Additionally, you will collaborate with cross-functional teams to resolve data discrepancies and mentor junior staff in data cleaning and reconciliation procedures.
Conduct diagnostic assessments and provide individual psychotherapy sessions via secure telehealth platforms. Maintain clear clinical documentation and coordinate care within a multidisciplinary team environment.
Conduct intake assessments and facilitate virtual individual and group counseling sessions using evidence-based curricula. Maintain accurate documentation in the EMR and collaborate with clinical supervisors on treatment planning and crisis support.
You will lead and coordinate external clinical supply packaging and distribution activities to ensure the successful delivery of clinical trial materials. This includes managing third-party contractors, overseeing documentation, and ensuring compliance with quality standards and study timelines.
The specialist will process and triage Individual Case Safety Reports (ICSRs) while ensuring data accuracy and regulatory compliance within safety databases. They will also perform literature screening, MedDRA coding, and maintain documentation for clinical trials and post-marketing programs.
The Clinical Specialist reviews assessment quality and provides guidance to raters on methodology and scoring techniques. They also participate in calibration activities and ensure the integrity of clinical trial data through live interactions and documentation.
The Clinical Trials Associate provides administrative and project tracking support to the clinical project team to ensure tasks are completed accurately. They are responsible for maintaining project documentation, managing system access, and performing quality audits on trial-related files.
The Senior Clinical Data Manager leads end-to-end data management activities for clinical studies, ensuring compliance with protocols, budgets, and timelines. They also provide mentorship to junior staff, manage sponsor relationships, and drive process improvements within the Biometrics department.
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The Clinical Data Manager oversees all aspects of the clinical trial data management process from study startup to database lock. They are responsible for database development, quality control, and ensuring data integrity while managing timelines and cross-functional team communication.
The Clinical Data Manager oversees the entire clinical trial data management process from study startup to database lock. They are responsible for database development, quality control, medical coding, and ensuring compliance with regulatory directives and study plans.
Conduct site qualification, monitoring, and close-out visits while ensuring protocol compliance and patient safety. Collaborate with site staff to manage clinical data and contribute to the preparation of study documentation and reports.
The Medical Director will lead medical safety evaluation and risk management efforts, including the review of adverse events and clinical outcomes. They will also provide medical consultation to the team, manage signal detection activities, and ensure compliance with regulatory guidelines.
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