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The Case Manager will work telephonically with patients and care teams to manage complex health needs and ensure appropriate benefit administration. They will apply clinical judgment to develop care plans, reduce risk factors, and facilitate multidisciplinary case conferences.
The instructor will teach undergraduate courses in the research ecosystem minor and develop course content including syllabi and assignments. They are also responsible for assessing student performance, holding office hours, and participating in collaborative instructional meetings.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits to ensure protocol compliance. Additionally, you will collaborate with investigators and site staff while performing data review to maintain high-quality clinical data.
The clinician will remotely administer semi-structured clinical interviews and cognitive test batteries to study subjects using a tele-health platform. They are also responsible for scoring assessments and providing central monitoring reviews to ensure data accuracy and quality.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to pediatric subjects and their caregivers. They are also responsible for scoring assessments and providing central monitoring to ensure data accuracy throughout clinical trials.
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The Veterinary Medical Officer conducts disease surveillance, investigates potential foreign animal diseases, and manages emergency response operations. They also collaborate with stakeholders to implement regulatory actions and provide expert guidance on animal health and public safety.
The clinician performs clinical reviews to assess the medical appropriateness of mental health and substance abuse services. They also conduct prior authorizations, concurrent reviews for inpatient care, and engage with providers to ensure efficient treatment planning.
The clinician will remotely administer semi-structured clinical interviews and cognitive assessment batteries to study subjects. They are also responsible for scoring assessments and providing central monitoring of neuropsychological test data to ensure accuracy.
You will collaborate with the content and research team to plan and execute clinical studies for digital health applications. Additionally, you will manage study participants and handle communication with psychotherapists according to defined processes.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. This includes conducting site visits, resolving performance issues, and collaborating with cross-functional teams to ensure accurate data collection.
The Clinical Trial Manager will oversee daily operations, logistics, and vendor management for outsourced clinical trials. They are responsible for trial status tracking, risk management, and ensuring compliance with ICH and GCP regulatory requirements.
The role involves conducting patient interviews and clinical assessments while ensuring the integrity and reliability of clinical trial data. The rater will provide guidance to other raters on methodology and scoring techniques through live interactions.
The Registered Nurse will assess and triage patient needs via phone and in-office visits while providing clinical guidance and care coordination. They will also manage medication refills, test results, and support patients through transitions of care and chronic disease management.
The Clinical Specialist reviews clinical trial data and assessment scales to ensure standardized practices and data integrity. They also conduct live interactions with raters to provide guidance on methodology, scoring techniques, and performance support.
The freelance study nurse will conduct study-related visits via video or telephone and support the digital informed consent process. They will also assist with documentation and serve as a point of contact for non-medical participant inquiries.
The Clinical Research Associate will coordinate clinical trial monitoring activities, maintain study documentation, and ensure compliance with protocols and regulatory requirements. They will also manage stakeholder relationships and oversee study cost efficiency to ensure high-quality clinical outcomes.
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You will provide clinical support and consultation to medical staff regarding the CARTO 3 navigation system during electrophysiological procedures. Additionally, you will act as a primary point of contact for the product portfolio, managing customer relationships and driving the development of electrophysiology labs.
Performs clinical evaluations on medical claims to ensure documentation substantiates the need for employee absence. Acts as a clinical resource for claims examiners and provides guidance on medical management and claim decisions.
Translate and edit healthcare-related documents from German to English for a major client. Collaborate with a dedicated team of linguists to ensure high-quality localization and professional excellence.
The Clinical Research Associate II is responsible for monitoring clinical study sites to ensure data integrity, patient safety, and adherence to regulatory standards. They will manage site activities, maintain Trial Master File documentation, and conduct qualification, initiation, and close-out visits.
You will support the management of clinical trial sites in compliance with ICH-GCP and study protocols while participating in site initiation, monitoring, and close-out visits. Additionally, you will conduct source data verification and assist cross-functional teams in ensuring data quality and patient safety.
Perform manual, independent reviews of recorded clinical trial interviews and scale administrations to ensure scoring accuracy and protocol adherence. Senior roles also involve clinical decision-making regarding site performance and overseeing rater remediation.
You will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. Key tasks include monitoring clinical trial sites, conducting site visits, and collaborating with cross-functional teams to ensure accurate data collection.
The Clinical Application Specialist acts as a clinical expert for angiography systems, providing hands-on training and support to medical professionals. They also assist the sales team by providing clinical expertise and contributing to the development of successful sales strategies.
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The Senior Clinical Research Associate is responsible for independently setting up, monitoring, and closing out clinical study sites while ensuring adherence to ICH-GCP regulations. They will also manage regulatory submissions, handle sponsor queries, and contribute to study documentation and feasibility assessments.
The Senior Director leads analytic service delivery by aligning strategic objectives with tool development and managing cross-functional analytic teams. They partner with clinical and business leaders to drive data-informed decision-making, performance improvement, and value realization across the enterprise.
You will conduct clinical trial monitoring activities, including site qualification, initiation, and close-out visits. Additionally, you will ensure protocol compliance, maintain data integrity, and collaborate with site staff to facilitate study conduct.
You will advise participants on training opportunities and manage the administrative processing of online and on-campus seminars. Additionally, you will assist with preparatory accounting and contribute to the development of customer communication strategies.
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