Emmes Group

Technical Project Manager I, II & III - Essex Management (Contingent Role)

Emmes Group · Full Time · 7 days ago

Emmes Group

🌎 United States ⭐ 10+ yrs exp 💼 Product

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.

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Senior Study Start-Up Associate

Emmes Group · Full Time · 8 days ago

Emmes Group

🌎 United States ⭐ 5-10 yrs exp 💼 Others

The Senior Study Start-up Associate manages the preparation and submission of regulatory packages to ensure clinical trial alignment with global and local requirements. They coordinate site activation, maintain regulatory trackers, and serve as a primary contact for sponsors and regulatory authorities.

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In-House Clinical Research Associate- Government

Emmes Group · Full Time · 8 days ago

Emmes Group

🌎 United States ⭐ 0-2 yrs exp 💼 Healthcare

The In-House CRA supports site management and monitoring activities to ensure clinical trials comply with protocols, SOPs, and regulatory requirements. Key tasks include maintaining essential documents in the Trial Master File and tracking trial progress via the CTMS.

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Manager - Global Clinical Project Management

Emmes Group · Full Time · 8 days ago

Emmes Group

🌎 India ⭐ 10+ yrs exp 💼 Product

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.

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In-House Clinical Research Associate

Emmes Group · Full Time · 11 days ago

Emmes Group

🌎 United States ⭐ 0-2 yrs exp 💼 Healthcare

The In-House CRA supports site management and monitoring activities to ensure clinical trials comply with protocols, SOPs, and regulatory requirements. Key tasks include maintaining essential documents in the Trial Master File and tracking trial progress via CTMS.

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Manager, Statistical Programming

Emmes Group · Full Time · 15 days ago

Emmes Group

🌎 India ⭐ 5-10 yrs exp 💼 Others

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.

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Sr. Clinical Application Administrator - Clinevo

Emmes Group · Full Time · 17 days ago

Emmes Group

🌎 India ⭐ 5-10 yrs exp 💼 Software Development

Administer and maintain enterprise clinical applications to ensure high availability, security, and performance. Lead system upgrades, user access governance, and collaborate with stakeholders to optimize application usage.

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Clinical Trial Manager II

Emmes Group · Full Time · 17 days ago

Emmes Group

🌎 United States ⭐ 5-10 yrs exp 💼 Healthcare

The Clinical Trial Manager II oversees operational activities and site monitoring for clinical studies to ensure timelines and quality standards are met. They lead monitoring teams, develop key study plans, and serve as the primary operational point of contact for clients and sponsors.

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Controlled Documents Specialist

Emmes Group · Full Time · 19 days ago

Emmes Group

🌎 Brazil, Colombia, Panama ⭐ 2-5 yrs exp 💼 Others

Manage the full lifecycle of controlled documents within the Veeva Quality platform to ensure regulatory compliance and quality standards. Support stakeholders in document creation and maintain audit readiness through accurate classification and metadata management.

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Senior Statistical Programmer

Emmes Group · Full Time · 21 days ago

Emmes Group

🌎 India ⭐ 2-5 yrs exp 💼 Software Development

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.

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Events & Demand Generation Lead 

Emmes Group · Full Time · 21 days ago

Emmes Group

🌎 United States ⭐ 2-5 yrs exp 💼 Marketing

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.

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Medical Officer

Emmes Group · Full Time · 22 days ago

Emmes Group

🌎 United States ⭐ 2-5 yrs exp 💼 Healthcare

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.

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Independent Lead Generation & Pipeline Development Consultant (Europe) – Veridix AI (Contractor)

Emmes Group · Full Time · 24 days ago

Emmes Group

🌎 Spain ⭐ 10+ yrs exp 💼 Software Development

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.

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Executive Assistant

Emmes Group · Full Time · 25 days ago

Emmes Group

🌎 India ⭐ 2-5 yrs exp 💼 Virtual Assistant

Provide high-level administrative support to executives within a clinical research organization. Assist in managing operations to help advance medical discovery and patient care.

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Business Systems Engineer I & II - Essex Management (Contingent Roles)

Emmes Group · Full Time · a month ago

Emmes Group

🌎 United States ⭐ 5-10 yrs exp 💼 Software Development

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.

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Business Systems Architect - Level 2 - Essex Management (Contingent Role)

Emmes Group · Full Time · a month ago

Emmes Group

🌎 United States ⭐ 5-10 yrs exp 💼 Software Development

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.

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Proposal Manager

Emmes Group · Full Time · a month ago

Emmes Group

🌎 United States ⭐ 2-5 yrs exp 💼 Others

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.

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Project Leader - Biostatistician

Emmes Group · Full Time · a month ago

Emmes Group

🌎 United States ⭐ 5-10 yrs exp 💼 Healthcare

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.

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CRAII

Emmes Group · Full Time · a month ago

Emmes Group

🌎 India ⭐ 0-2 yrs exp 💼 Others

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.

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Senior Biostatistician

Emmes Group · Full Time · a month ago

Emmes Group

🌎 United States ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Senior Biostatistician Manager

Emmes Group · Full Time · a month ago

Emmes Group

🌎 United States ⭐ 10+ yrs exp 💼 Healthcare

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.

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Associate Project Leader - Vaccines & Infectious Diseases

Emmes Group · Full Time · a month ago

Emmes Group

🌎 United States ⭐ 5-10 yrs exp 💼 Others

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.

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Clinical Data Manager - Temp to Perm

Emmes Group · Part Time · a month ago

Emmes Group

🌎 United States ⭐ 2-5 yrs exp 💼 Healthcare

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.

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Safety Manager - Cell and Gene

Emmes Group · Full Time · 2 months ago

Emmes Group

🌎 United States ⭐ 5-10 yrs exp 💼 Others

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.

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Quality Assurance Analyst - Essex Management (Contingent Role)

Emmes Group · Full Time · 2 months ago

Emmes Group

🌎 United States ⭐ 2-5 yrs exp 💼 Software Development

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.

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Clinical Systems Business Analyst (Jr & Mid) – Multiple Openings - Essex Management (Contingent Role)

Emmes Group · Full Time · 2 months ago

Emmes Group

🌎 United States ⭐ 2-5 yrs exp 💼 Software Development

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.

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Senior Clinical Research Associate

Emmes Group · Full Time · 2 months ago

Emmes Group

🌎 United States ⭐ 5-10 yrs exp 💼 Healthcare

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.

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Project Manager – Level I - Essex Management (Contingent Role)

Emmes Group · Full Time · 2 months ago

Emmes Group

🌎 United States ⭐ 2-5 yrs exp 💼 Product

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.

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Clinical Research Associate II

Emmes Group · Full Time · 2 months ago

Emmes Group

🌎 United States ⭐ 2-5 yrs exp 💼 Healthcare

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.

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Sr. Software Development Engineer - Veridix AI

Emmes Group · Full Time · 2 months ago

Emmes Group

🌎 United States ⭐ 2-5 yrs exp 💼 Software Development

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.

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