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Manage all laboratory aspects of clinical trial projects from award through closeout, serving as the primary point of contact for sponsors. Lead study set-up, monitor project timelines and budgets, and coordinate cross-functional resources to ensure high-quality execution.
The Senior Clinical Trials Associate manages clinical study documentation, maintains the electronic Trial Master File, and ensures FDA readiness. They also coordinate with study sites, vendors, and sponsors while supporting project teams and training new staff.
The Clinical Trial Manager is responsible for leading clinical study site management activities and coordinating a team of clinical staff within a geographic region. They ensure site qualification, initiation, monitoring, and close-out activities are conducted in compliance with study protocols and standard operating procedures.
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.
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety and regulatory compliance. Collaborates with functional leaders to coordinate study milestones and ensures the clinical team adheres to protocol and risk mitigation strategies.
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The Associate Medical Director provides medical oversight for clinical trials, ensuring compliance with regulatory requirements and company SOPs. They also manage safety variables, perform medical reviews of adverse events, and provide medical consultation to project teams and clients.
The Senior Clinical Research Associate is responsible for managing research activities at clinical sites, including study start-up, site training, and maintenance. They ensure compliance with regulatory requirements, manage informed consent processes, and oversee safety-related event reporting.
The virtual assistant will manage patient communications, including phone calls and emails, while assisting with medication refill requests and scheduling inquiries. Additionally, the role involves maintaining standard operating procedures to support the practice's transition to a cash-based model.
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 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 Programmatic Media Manager is responsible for driving performance, strategy, and account growth for major multi-channel paid media clients. This role involves executing media campaigns, managing budgets, and serving as the primary point of contact for client communication and reporting.
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 Clinical Research Associate will coordinate study setup and monitoring activities while ensuring high-quality outcomes and accurate documentation. They are responsible for maintaining strong relationships with stakeholders and ensuring strict compliance with protocols to protect patient safety.
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 Senior Clinical Trial Coordinator is responsible for overseeing and coordinating clinical trial activities to ensure compliance with protocols and regulatory standards. They will manage trial documentation, facilitate communication between study sites and sponsors, and ensure the timely completion of project milestones.
The Clinical Trial Coordinator II provides administrative and technical support for clinical trials, including site activation, regulatory document management, and file reviews. They ensure trial activities are completed on time and within budget while maintaining compliance with SOPs and regulatory guidelines.
The In-House Clinical Research Associate II is responsible for managing clinical study sites in accordance with GCPs and regulatory requirements. They provide support to project teams, maintain study documentation, and assist with remote monitoring and data management tasks.
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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.
The Senior Clinical Data Manager leads multiple clinical studies, ensuring accurate data collection, management, and reporting in compliance with regulatory requirements. They are responsible for EDC system development, vendor oversight, data cleaning, and mentoring junior team members.
The Lead Clinical Research Associate oversees clinical study teams, ensuring high-quality execution, compliance, and timely delivery of trial activities. They provide mentorship, manage project timelines, and act as the primary point of coordination across cross-functional teams.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data reliability. You will provide feedback on methodology and scoring while maintaining accurate documentation for clinical trial activities.
The role involves administering clinical assessments to trial participants and evaluating the quality of assessments performed by other raters to ensure data standardization. You will provide feedback on scoring techniques, manage documentation, and conduct remote interactions with participants and raters.
The Senior Clinical Research Associate coordinates clinical monitoring and site management processes to ensure protocol compliance and data reliability. They perform risk-based monitoring, manage site documentation, and facilitate communication between investigative sites and project teams.
You will lead clinical research tasks by creating data management plans, ensuring regulatory compliance, and resolving data discrepancies. Additionally, you will collaborate with cross-functional teams and mentor junior staff to maintain high data quality standards.
Manage a portfolio of healthcare partners to secure and maintain clinical placements for MRI students. This involves outbound prospecting, reactivating dormant accounts, and coordinating student placements with hospital and imaging center leadership.
The Clinical Trial Manager is responsible for planning and managing all aspects of clinical trials, ensuring adherence to timelines, budgets, and quality standards. They collaborate with cross-functional teams and investigators to implement protocols and ensure compliance with international regulations.
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Monitor clinical trial sites through on-site and remote visits while maintaining strong relationships with investigators. Ensure study integrity by managing documentation and keeping sites audit- and inspection-ready.
Accountable for the strategic development and delivery of decentralized and hybrid clinical trials while optimizing speed, quality, and cost. This role involves managing customer relationships, overseeing project financials, and collaborating across functional teams to ensure regulatory compliance.
The Senior CRA coordinates clinical monitoring and site management to ensure trial compliance with protocols, ICH-GCP guidelines, and regulatory requirements. Responsibilities include conducting remote or on-site visits, managing documentation, and maintaining collaborative relationships with investigational sites.
The Lead CRA provides leadership and oversight to the CRA and CTA teams to ensure the accurate and timely conduct of clinical trials. They serve as the primary liaison between study sites, internal staff, and clients while managing clinical monitoring plans and quality issues.
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