The role involves leading biostatistical efforts to advance clinical research and medical discovery. The Associate Director will support various therapeutic areas including cell and gene therapy and infectious diseases.
Emmes Group
32 Remote Job Openings at Emmes Group
Leads the delivery of complex, technology-enabled clinical certification studies and imaging programs while managing client expectations and study-level outcomes. Provides functional leadership by mentoring staff and driving process improvements to enhance operational scalability.
The Clinical Trial Manager I leads operational activities for clinical studies, overseeing monitoring teams and ensuring timelines and quality standards are met. They are responsible for site management, developing key study plans, and maintaining relationships with clients and vendors.
Provide lead statistical programming support for complex clinical research projects using advanced SAS techniques. Ensure regulatory-compliant output, develop programming documentation, and mentor junior staff.
The role involves administering and maintaining enterprise clinical applications to ensure high availability, security, and performance. Key duties include managing user access, implementing system upgrades, and collaborating with stakeholders to optimize application usage.
The In-House CRA supports site management and monitoring activities to ensure clinical trials comply with protocols, SOPs, and regulatory requirements. Key duties include maintaining essential documents in the Trial Master File and tracking trial progress via CTMS.
The Senior CRA is responsible for monitoring clinical study sites remotely and on-site to ensure trials are conducted according to protocols, SOPs, and ICH GCP guidelines. Key duties include conducting site visits, verifying source data, and managing action item resolution to ensure regulatory compliance.
The CRA II is responsible for monitoring clinical study sites remotely and onsite to ensure trials are conducted according to protocols, SOPs, and ICH GCP guidelines. Key duties include conducting site visits, verifying source data, and managing site staff training and compliance.
Technical Project Manager I, II & III - Essex Management (Contingent Role)
Emmes Group
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Full Time
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a month ago
Emmes Group
Manage and lead technical projects throughout their lifecycle, ensuring delivery on time, within budget, and in compliance with regulatory requirements. Responsibilities range from project coordination and documentation for Level I to strategic portfolio leadership and governance for Level III.
Oversee the delivery of global clinical trial operations by managing staff development, resource allocation, and operational efficiency. Act as a key escalation point to ensure quality, compliance, and financial management across projects.
The role provides lead oversight for statistical programming on complex clinical projects, ensuring timely delivery of regulatory submission deliverables. It involves managing staff, mentoring team members, and implementing standardized programming best practices.
The role involves designing and developing SAS programs to analyze clinical data and create tables, figures, and listings. Responsibilities include writing documented code, developing macros, and resolving data inconsistencies to ensure reproducible results.
Manage the end-to-end planning and execution of industry conferences and trade shows to enhance brand visibility. Convert event touchpoints into commercial opportunities through lead qualification and pipeline development for biopharma sponsors.
The Medical Officer is responsible for medical monitoring of clinical trials, including safety oversight and the evaluation of adverse events. They provide medical consultancy for protocol development, bid preparation, and engagement with safety oversight committees.
Independent Lead Generation & Pipeline Development Consultant (Europe) – Veridix AI (Contractor)
Emmes Group
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Full Time
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a month ago
Emmes Group
The consultant will independently design and execute lead generation strategies to identify and qualify new business opportunities within the European biotech and pharma markets. Key tasks include conducting outbound outreach, monitoring market intelligence, and passing qualified leads to internal commercial teams.
Provide high-level administrative support to executives within a clinical research organization. Assist in managing operations to help advance medical discovery and patient care.
Business Systems Engineer I & II - Essex Management (Contingent Roles)
Emmes Group
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Full Time
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2 months ago
Emmes Group
Apply process improvement and business process reengineering methodologies to modernize clinical informatics and health IT environments. Analyze current-state workflows to design future-state solutions and lead the transition to automated, technology-enabled business processes.
Business Systems Architect - Level 2 - Essex Management (Contingent Role)
Emmes Group
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Full Time
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2 months ago
Emmes Group
Lead large-scale business process reengineering and modernization initiatives within Life Sciences and Clinical Informatics programs. Coordinate between client delivery and project teams to design scalable, technology-enabled solutions and ensure alignment with organizational goals.
Lead proposal teams in developing high-quality, compliant biomedical research proposals for the U.S. government and other organizations. Manage the end-to-end proposal process, including shredding requirements, writing content, and coordinating with SMEs and pricing teams.
The Project Leader - Biostatistician serves as the matrix leader for government-sponsored clinical research projects, managing the core project team and ensuring delivery within timeline and budget. They are responsible for statistical leadership, client relationship management, and the continuous monitoring and mitigation of project risks.
The CRA II is responsible for monitoring clinical study sites remotely and on-site to ensure trials are conducted according to protocols, SOPs, and ICH GCP guidelines. Key tasks include conducting site visits, verifying source data, and managing action item resolution post-visit.
Leads collaborations with clinical investigators to determine study design, develop protocols, and author statistical analysis plans. Manages statistical activities for clinical studies and presents findings in reports and peer-reviewed journals.
Oversees statistical activities and deliverables across a broad research area while managing a team of Biostatistician Managers. Serves as the primary statistical expert and client point of contact for large projects, ensuring high-quality and timely completion of deliverables.
Associate Project Leader - Vaccines & Infectious Diseases
Emmes Group
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Full Time
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2 months ago
Emmes Group
The Associate Project Leader serves as the matrix leader for government-sponsored clinical research projects, ensuring deliverables are met within timeline and budget. They act as the primary point of contact for clients and stakeholders while coordinating across various internal departments to execute project goals.
The Data Manager oversees data management activities throughout the research study lifecycle, from design to closeout. Key duties include designing eCRFs, managing data validation, and ensuring the accuracy and completeness of study data in electronic databases.
The Safety Manager implements Pharmacovigilance and Medical Monitoring activities, supervising Safety Monitors and managing safety reporting for clinical projects. They ensure adherence to Good Pharmacovigilance Practices and coordinate safety-related documentation and regulatory submissions.
Quality Assurance Analyst - Essex Management (Contingent Role)
Emmes Group
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Full Time
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2 months ago
Emmes Group
Provide technical and administrative oversight of software development to ensure compliance with federal, GxP, and FDA standards throughout the SDLC. Conduct quality assessments, risk-based validations, and formal reviews to ensure data integrity and system reliability.
Clinical Systems Business Analyst (Jr & Mid) – Multiple Openings - Essex Management (Contingent Role)
Emmes Group
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Full Time
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2 months ago
Emmes Group
The role acts as a bridge between clinical operations and technical teams to translate business needs into functional specifications. Responsibilities include leading stakeholder workshops, documenting workflows, and supporting system implementation and validation.
The Senior Clinical Research Associate will contribute to the advancement of clinical research by supporting various medical discovery projects. They will work collaboratively within a performance-driven environment to embed innovation into company processes.
Project Manager – Level I - Essex Management (Contingent Role)
Emmes Group
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Full Time
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2 months ago
Emmes Group
The Project Manager I leads assigned projects or workstreams through the full lifecycle, ensuring alignment with contractual scope and organizational objectives. They coordinate cross-functional teams, manage project documentation, and mitigate risks to ensure successful delivery.
The Clinical Research Associate II is responsible for monitoring clinical study sites to ensure trials are conducted in accordance with protocols, SOPs, and regulatory requirements. They perform site visits, conduct source data verification, and facilitate the resolution of action items while maintaining compliance with ICH GCP standards.
Design, develop, and enhance cloud-based, SaaS web-based clinical trial applications while collaborating with cross-functional teams. Ensure code quality through unit testing, debugging, code reviews, and technical documentation while mentoring junior team members.
