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The Research Director will own client relationships and create research strategies to embed data into client workflows while driving account growth. They will also manage large, complex research projects and mentor team members to ensure high-quality delivery and strategic insights.
The Initiation Clinical Research Associate leads and executes study start-up, site activation, and regulatory submission activities. They act as the primary contact for assigned sites to ensure compliance and maintain high-quality documentation throughout the study lifecycle.
The Global Study Manager acts as the primary liaison between clients, CROs, and internal teams to ensure seamless study delivery. They provide project management oversight, including budget, risk, and milestone management, while maintaining high-quality client service.
The Research Analyst Engineer is responsible for researching, gathering, and organizing technical hardware and software specifications for internal databases. They will also fact-check data, edit content for web publication, and ensure all information meets quality guidelines.
Design and implement optimization models and a production-grade scheduling solver for workforce planning, scheduling, and resource allocation in a large-scale contact center environment. Validate schedule quality and solver performance, integrate the service into the WFM platform, and collaborate with business and engineering stakeholders to ensure schedules are operationally usable.
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Support the finalization of the TIFA-TCG evaluation by reviewing documents, extracting evidence, managing stakeholder comments, refining analysis, and assisting with targeted consultations. Help quality-check report materials, revise and format the report, manage data and references, and provide administrative coordination.
Manage site activities and supervise assigned oncology studies for a dedicated client, including independent monitoring across all types of visits. Collaborate with sponsors and subject matter experts, and mentor junior CRAs as appropriate.
The Associate Director will drive clinical research and real-world evidence generation activities to support product development, regulatory submissions, and market access. They will collaborate with cross-functional teams to design study protocols, interpret clinical data, and manage scientific communications.
The Market Research Specialist will identify and qualify high-quality leads across Web3, AI, and fintech sectors to fuel the sales pipeline. They will manage CRM data, collaborate with the sales team, and continuously improve research processes to meet business growth goals.
You will be responsible for all site management and supervisory activities for assigned oncology studies while working with industry leaders. Additionally, you will mentor junior CRAs and ensure compliance with clinical research legislation and guidelines.
You will conduct clinical trial monitoring activities including site qualification, initiation, and close-out visits to ensure protocol compliance and patient safety. Additionally, you will perform data review, resolve queries, and contribute to the preparation of study documentation and clinical study reports.
Perform site selection, initiation, monitoring, and close-out visits while maintaining accurate study documentation. Manage study progress by tracking regulatory submissions, recruitment, and data query resolution.
Interns will contribute to experimental design, data analysis, and academic writing for research projects in FinTech and AI. They will take responsibility for specific research tasks and assist in preparing manuscripts for top-tier academic venues.
The Research Analyst Engineer will search for and analyze technical data regarding hardware and software to maintain internal databases. Additionally, they will write, edit, and fact-check content for publication while ensuring it meets company tone and quality standards.
Monitor clinical trial sites and conduct site visits to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Coordinate with cross-functional teams, resolve site issues, support accurate data collection, and train site staff and other CRAs.
Develop new Knowledge & Research Services engagements by building market relationships, understanding client needs, shaping scopes and proposals, and supporting commercial decisions. Oversee Interim Research performance and P&L, align engagement handoffs and delivery, and lead BLISS, LINKS, market engagement, and the practice’s thought leadership.
The Clinical Project Research Manager is responsible for planning, organizing, and leading project teams to deliver clinical research projects on time and within budget. They oversee all operational aspects from start-up through close-out while serving as the primary contact for sponsors and managing cross-functional project teams.
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The Research Nurse will coordinate and complete subject trial visits both on-site and off-site while ensuring adherence to trial protocols and SOPs. They are responsible for accurate data documentation, administration of trial medication, and the reporting of adverse events to the project management team.
Support pre-award and post-award financial activities for clinical research departments, including oversight of research-related hospital and physician bills, revenue and expense accuracy, clinical trial modeling, and accounts receivable. Develop management reports, assist with research budget preparation and negotiation, and collaborate with research, entity, and Finance teams to provide insights for decision-making.
The Senior Research Analyst conducts complex, high-impact research to support congressionally mandated reporting on international labor abuses and supply chains. The role also involves providing technical guidance and mentorship to junior analysts while developing findings and recommendations for senior leadership.
The Hotline Operator provides 24/7 crisis intervention and referral services for individuals at risk of opioid overdose using a harm reduction framework. They also manage data collection, assist patients with treatment access, and collaborate with healthcare providers to support program improvements.
Verify source documents and conduct pre-study, initiation, monitoring, and termination site visits while ensuring compliance with FDA, ICH-GCP, and local regulations. Support budget follow-up, data validation and query resolution, regulatory document collection, and mentoring junior team members as needed.
The Clinical Research Associate will lead performance and compliance for assigned protocols and sites, serving as the primary contact for clinical studies. They are responsible for conducting remote and on-site monitoring to ensure data integrity, subject safety, and adherence to ICH/GCP standards.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP regulations. Additionally, you will coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
You will monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP regulations. Additionally, you will coordinate study setup activities, including identifying investigators and preparing regulatory submissions.
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Conduct quantitative analysis across multiple sexual and reproductive health research and evaluation projects, including data cleaning, statistical modeling, data quality monitoring, and preparation of reports and research products. Contribute to research design and data collection, coordinate analysis timelines, present findings, and guide research assistants.
You will oversee and manage clinical trial activities to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice standards. Additionally, you will conduct site visits, resolve performance issues, and provide training to site staff to ensure successful trial execution.
The Research Nurse will manage day-to-day clinical trial activities, including protocol adherence, data documentation, and patient care both on-site and off-site. They are responsible for administering trial medication, processing samples, and reporting adverse events to ensure patient safety and data integrity.
Analyze mobile games to document ad placement, player journeys, and monetization patterns. Translate raw gameplay and log data into structured research notes to support product and engineering teams.
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