Work When You Want Paid Research Studies - Davie, FL
Participants will share their opinions through online surveys, video focus groups, and product testing. They will provide feedback on various ads, apps, and services.
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Participants will share their opinions through online surveys, video focus groups, and product testing. They will provide feedback on various ads, apps, and services.
Conduct independent and collaborative research evaluating precision screening and prevention strategies using large healthcare datasets, statistical methods, machine learning, AI, and health economic analyses. Publish and present findings, contribute to grants and scientific reporting, and collaborate with multidisciplinary research partners.
Manage research activities at investigative sites throughout the clinical study lifecycle, including start-up, maintenance, and closeout. Ensure study compliance with regulatory requirements, informed consent, and safety reporting while collaborating with study teams.
Mentor undergraduate students through the entire research process, including topic selection, study design, and execution. Provide structured feedback on research plans, data interpretation, and written drafts to ensure academic quality.
Contribute expertise to help research models understand and interpret Jyotish as an experienced practitioner would. Explain the reasoning behind chart readings and astrological analyses.
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Participate in paid online or video focus groups, surveys, and at-home product tests. Share feedback on advertisements, apps, services, and other products.
Independently conduct and oversee clinical trial site monitoring, including site qualification, initiation, interim, and close-out visits, while ensuring protocol, GCP, regulatory, and quality compliance. Guide and mentor CRA colleagues, review monitoring documentation and trial data, resolve site issues, and coordinate with sponsors and cross-functional teams on study delivery.
Conduct and oversee clinical trial site monitoring, including site visits, source data verification, regulatory document review, investigational product accountability, and adverse event reporting. Guide and mentor CRA colleagues, support study planning and site issue resolution, and ensure compliance with protocols, ICH GCP, regulations, and applicable SOPs.
Conduct and oversee clinical trial site monitoring, including qualification, initiation, interim, and close-out visits, while ensuring protocol, GCP, regulatory, and quality compliance. Guide and mentor CRA team members, manage site issues and sponsor communications, and support trial documentation, data integrity, recruitment, and study operations.
Lead U.S. and global qualitative and quantitative research projects, from defining objectives and selecting methods through fieldwork, analysis, and reporting. Synthesize primary, syndicated, secondary, and unstructured customer data into actionable recommendations, while managing vendors and partnering with stakeholders to inform business decisions.
Independently manage, analyze, draft, negotiate, and execute complex industry-funded research agreements while balancing institutional compliance, project needs, and protection of intellectual property. Advise and collaborate with researchers, sponsors, and internal offices; provide training and subject matter expertise; and contribute to policy development and process improvement.
Recruit and prescreen potential clinical research participants, match them to active or upcoming studies, and schedule research appointments. Maintain participant records and medical histories in Clinical Conductor, track recruitment trends, and create IRB-approved outreach and recruitment materials.
The associate will support teams in conducting technical assistance, data analytics, and program evaluation across various Medicaid policy areas. Responsibilities include maintaining technical documentation, performing quantitative analyses, and providing operational support to ensure projects remain on schedule and within budget.
Develop and lead an integrated content and research strategy for HR and talent professionals, producing editorial content, research publications, learning programs, and conference and webinar programming. Represent the organization as a subject-matter expert, build relationships with practitioners and speakers, support leadership councils, and lead a collaborative team while improving audience engagement.
Participants will engage in online surveys, focus groups, and product testing to provide feedback on various services and products. They are responsible for completing their panel profile to receive relevant study invitations.
The Clinical Research Associate is responsible for managing site relationships, ensuring protocol compliance, and overseeing the quality and integrity of clinical trial data. They conduct various site visits, including qualification, initiation, monitoring, and termination, while protecting the rights and well-being of trial subjects.
Build historical financial models and conduct company, industry, and macroeconomic research to support investment theses and recommendations. Develop client and industry relationships, prepare research reports and presentations, and collaborate across products to strengthen analysis and corporate access.
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The Director of Research will lead and scale the Beeck Center's applied research portfolio, focusing on digital transformation and public service delivery. They are responsible for defining strategic research directions, managing cross-functional teams, and translating practitioner insights into actionable policy recommendations.
Conduct and oversee clinical trial site monitoring, including qualification, initiation, interim, and close-out visits, while ensuring protocol, GCP, regulatory, and quality compliance. Guide and mentor CRA colleagues, resolve site and study issues, support trial documentation and reporting, and coordinate with sponsors and cross-functional teams.
The consultant will conduct qualitative research, including in-person interviews and observations in West Kalimantan, to capture the experiences of program participants. They are responsible for transcribing data, analyzing findings, and drafting a 3,000-word article that highlights the program's impact and participant challenges.
Lead end-to-end quantitative research engagements, including study design, fieldwork, analysis, and reporting for technology and gaming clients. Act as a strategic advisor to clients while managing multiple complex projects and supporting business development efforts.
Conduct and oversee clinical trial site monitoring, including site visits, source data verification, regulatory documentation, investigational product accountability, and adverse event reporting. Guide and mentor CRA colleagues, support study planning and budgets, resolve site issues, and ensure compliance with protocols, ICH GCP, regulations, and SOPs.
The Research Computing Services Manager provides technical and financial oversight for non-desktop computing infrastructure to support biomedical research. They lead teams across Linux, Windows, database, and storage domains to ensure efficient, secure, and reliable research operations.
The Senior Director leads a team of Account Managers to drive retention and growth across a $60M+ research program portfolio. They are responsible for managing renewal strategies, coaching staff on complex negotiations, and collaborating cross-functionally to improve partner outcomes.
The Contract Clinical Research Associate manages clinical study sites to ensure adherence to GCPs, SOPs, and regulatory requirements. They perform site monitoring visits, track subject recruitment, and maintain essential study documentation throughout the trial lifecycle.
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Conduct original research in generative AI and large language models applied to crypto and financial domains, focusing on reasoning under market uncertainty and multi-agent coordination. Design and execute rigorous experiments to develop novel post-training methodologies and evaluation frameworks for LLMs in adversarial financial environments.
Conduct in-depth research and risk assessments of various crypto projects to provide holistic insights. Analyze market trends and synthesize data from multiple sources to support informed decision-making.
The Research Analyst will conduct due diligence on issuers and partners while building commercial and financial models to evaluate product structures. They will also produce research memos and presentations to support key commercial decisions and track equity capital market developments.
The Clinical Research Associate performs on-site and remote monitoring activities to ensure investigational sites are adequately prepared and compliant. They are responsible for training site staff and supporting regulatory or ethics committee submissions.
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