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The Senior Clinical Data Associate performs activities for Phase I-III clinical trials to ensure data quality and adherence to timelines. Responsibilities include ongoing data review, reconciliation of third-party data, and performing user acceptance testing and quality control of clinical databases.
The Senior Clinical Data Associate performs data management activities for Phase I-III clinical trials, including data review and reconciliation. They are also responsible for conducting User Acceptance Testing (UAT) and Quality Control (QC) of clinical databases.
The coordinator manages the negotiation of confidentiality disclosure agreements and oversees the execution of site-level clinical trial agreements. They serve as the primary point of contact for investigative sites and vendors while ensuring all documentation meets quality and regulatory standards.
The Medical Director serves as the Global Lead Medical Monitor for clinical trials, providing therapeutic expertise and protocol-specific training to project teams. They also contribute medical input to clinical development programs and support business development activities through proposal generation and sponsor meetings.
The PMHNP provides comprehensive psychiatric assessment, diagnosis, treatment, and medication management within an integrated behavioral health setting. They also provide clinical oversight to care teams and collaborate with primary care providers to ensure high-quality patient outcomes.
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The Staff RN provides general nursing care to patients and families across the health-illness continuum while collaborating with a multidisciplinary team. Responsibilities include performing health assessments, documenting nursing interventions, and participating in process improvement to ensure clinical quality and safety.
The Staff RN provides general nursing care to patients and families across the health-illness continuum within a virtual ICU setting. They are responsible for performing health assessments, documenting nursing interventions, and collaborating with a multidisciplinary team to ensure patient safety and quality outcomes.
Manage the full lifecycle of clinical site payment administration, including protocol schedules, startup payments, and invoiceable items. Ensure accurate configuration of systems and resolve payment escalations to maintain site satisfaction and operational continuity.
Lead statistical strategy and delivery for complex clinical trials, ensuring high-quality outputs and regulatory compliance. Provide technical leadership, mentor junior staff, and collaborate with multidisciplinary stakeholders to support global programs.
The Senior Clinical Team Manager directs and coordinates the technical and operational aspects of clinical trials to ensure successful completion within budget and timelines. They manage clinical and start-up activities, lead project teams, and maintain compliance with ICH GCP and regulatory standards.
Perform manual, independent reviews of clinical trial interviews and scale administrations to ensure scoring accuracy and protocol adherence. Senior roles will also oversee site performance, interpret rater patterns, and manage targeted site interventions.
The Medical Director provides medical and scientific oversight for clinical research programs, serving as the primary medical monitor for sponsor-dedicated studies. Responsibilities include protocol development, safety monitoring, SAE reporting, and providing medical expertise to project teams throughout the clinical trial lifecycle.
Serve as the primary medical and scientific strategic lead for psychiatry-focused clinical studies and business development. Collaborate with cross-functional teams to design protocols, execute study strategies, and provide expert medical input for internal and external stakeholders.
The Staff RN provides general nursing care to patients and families across the health-illness continuum within a virtual ICU setting. Responsibilities include performing health assessments, documenting nursing interventions, and collaborating with a multidisciplinary team to ensure clinical quality and safety.
Lead day-to-day clinical trial operations from start-up through close-out while managing study timelines and enrolment targets. Provide oversight of CRA activities, ensure protocol compliance, and manage relationships with sponsors and investigators.
The Clinical Research Associate is responsible for conducting site visits, ensuring protocol compliance, and maintaining high-quality study documentation. They will also manage site relationships, support patient recruitment, and validate study data throughout the clinical trial lifecycle.
The Clinical Project Leader will provide cross-functional leadership for clinical trials, ensuring projects are delivered on time, within budget, and in compliance with ICH GCP standards. They are responsible for managing client relationships, project P&L, and mitigating risks throughout the project lifecycle.
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The Manager of Clinical Operations is responsible for leading the operational planning and execution of clinical trials to ensure they meet regulatory standards and timelines. They also focus on mentoring junior staff and collaborating with cross-functional teams to optimize trial design and operational efficiency.
The Principal Biostatistician will design and analyze clinical trials while overseeing statistical activities for programs and regulatory submissions. They will also manage day-to-day biostatistics operations, provide statistical consulting, and lead bid defense meetings with prospective clients.
Perform site selection, initiation, monitoring, and close-out visits while ensuring compliance with regulatory requirements. Manage study progress by tracking regulatory submissions, recruitment, and data query resolutions.
The Medical Director oversees the execution of clinical trials in Neuroimmunology, specifically focusing on Lupus SLE, for a top-5 pharma client. Responsibilities include developing clinical development plans, overseeing medical writing for protocols, and managing clinical teams and scientific risks.
The Clinical Team Manager oversees all clinical operational and quality aspects of respiratory studies in compliance with ICH-GCP. This includes developing monitoring strategies, managing project financials, and leading clinical teams to ensure deliverables are met within contractual timelines.
Manage the performance and workload of medical writers while overseeing the preparation and quality of publication deliverables. Lead resource planning, budget preparation, and the development of departmental training programs and SOPs.
Conduct 45-minute online psychological counseling sessions to help clients improve their mental well-being. Identify client needs and provide individualized, sustainable solutions for issues ranging from stress to career growth.
The role involves managing administrative tasks, triaging tickets and emails in Jira, and responding to payment queries from sites and sponsors. Additionally, the associate supports system migrations and study reconciliation activities through data preparation and tracking.
Provide medical leadership and support for clinical trials in nephrology, including protocol creation and real-time medical monitoring. Act as the primary medical liaison between the sponsor and internal departments to ensure subject safety and study compliance.
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The Director will engage with senior management to establish strategic department initiatives and drive business development activities for Clinical Assessment Technologies. They are also responsible for overseeing the development of assessment training content and ensuring all materials meet protocol and regulatory requirements.
The Clinical Research Associate II will conduct remote or on-site visits to assess protocol and regulatory compliance, manage documentation, and ensure trials adhere to approved protocols, ICH-GCP guidelines, and SOPs. Key duties involve monitoring investigator sites using a risk-based approach, identifying failures, implementing corrective actions, and ensuring data reliability.
The Principal Biostatistician serves as a resource for the statistical department, mentoring biostatisticians and overseeing training plans. They provide support across all statistical tasks during the project lifecycle and ensure high-quality work is completed on time.
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