This role will assist project teams in executing commercial and governmental clinical research initiatives. Execute responsibilities under clinical research managers' supervision. Develop, evaluate, and sustain project documentation per established guidelines. Collaborate with team members to diagnose challenges and propose potential resolutions. Interface with clients, sponsors, and site representatives to guarantee project objectives are fulfilled. Compensation: $25 - $27 Per Hour Essential Duties: • Implement foundational clinical research methodologies to satisfy protocol and regulatory standards. • Support client deliverable creation according to project specifications, including documentation, operational procedures, and workflow development with guidance from experienced personnel. • Manage incoming and outgoing project materials, monitoring, verifying, and tracking documentation distribution across internal and external research personnel. • Engage with clinical site staff regarding study activities, inquiries, and potential complications. • Conduct comprehensive quality assessments of documentation. • Generate correspondence, meeting agendas, minutes, reports, and project-specific documentation. Ensure thorough review, authorization, and distribution to internal and external participants. • Provide logistical support for committee and data safety monitoring board meetings, including planning, travel arrangements, post-meeting activities, and report generation. • Refresh tracking spreadsheets and tools to reflect current project status. • Recognize and investigate challenges, collaborating with experienced staff on corrective strategies. • Communicate activity status and potential issues to senior team members as appropriate. • Occasionally assist with data management tasks. • Maintain clinical research documentation and associated files. • Guarantee timely task completion and consistently high-quality work. • Execute additional assigned responsibilities. Minimum Qualifications: • Associates Degree - Bachelor's Preferred • 2 years of clinical research experience • Proficiency in Microsoft Office tools including Word, Excel, PowerPoint • Ability to function effectively in dynamic environments, managing substantial workloads and multiple concurrent projects • Exceptional interpersonal and communication capabilities • Strong decision-making and problem-solving skills • Superior organizational abilities with meticulous attention to detail MPF Federal is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status or on the basis of disability. We offer a competitive compensation package including a competitive salary, medical benefits, PTO, holiday pay and more.
United States Remote (Global)
MPF Federal is hiring a Remote - Research Assistant - Full Time
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