Sr. Project Leader

The Emmes Company, LLC; Rockville (MD); On-site; USD 1 - 2; Full time

Benefits offered by this job

Restaurant discounts

Job summary

The Emmes Company, LLC in Rockville, MD is seeking a Sr. Project Leader to drive complex, federally funded clinical research programs.

You will own project delivery, define milestones, and ensure study plans meet regulatory and quality standards. You will lead cross-functional teams (clinical operations, data management, biostatistics, regulatory), mentor junior project staff, and communicate progress with sponsors.

Qualifications

• Bachelor's Degree required; advanced degrees preferred.
• 12+ years with relevant PM experience in a research environment.
• Experience delivering complex clinical trials or federally-funded research preferred.
• Strong leadership, communication, and problem-solving skills.
• Ability to mentor and develop junior project leaders.

Responsibilities

• Lead assigned government funded protocols and research initiatives.
• Serve as primary client contact for project and protocols.
• Develop and oversee study protocols, SAPs, CSRs, and project plans.
• Ensure GCP, human subjects protections, and regulatory compliance.
• Provide direction on study design, endpoints, and risk mitigation.
• Coordinate with QA for audits and corrective actions.

Skills

Project management

Leadership

Communication

Cross-functional collaboration

Clinical research knowledge

Education

Bachelor's degree

Master's degree

PhD

Job description

Overview

Sr. Project Leader
Be Part of One Team, One Purpose.
At Emmes Group, we're shaping the future of clinical research-where human intelligence meets cutting-edge technology to drive meaningful advancements in healthcare. With over 47 years of scientific excellence, we've led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience.
Through our two business units-Emmes, a full-service CRO, and Veridix AI, our technology, data, and analytical solutions -we are modernizing clinical trials and accelerating the development of life-changing therapies.
We believe that every clinical breakthrough starts with people-people who are passionate, purpose-driven, and ready to make an impact. At Emmes Group, we bring People, Science, and Technology together to collaborate with our customers and deliver global health impact. Our culture is built on integrity, collaboration, and innovation, ensuring that every challenge is met with perseverance and accountability.

Responsibilities

• Serve as the lead for assigned government funded protocols and research initiatives.
• Serves as the client's, investigators' and other stakeholders' primary point of contact for the project and/or assigned protocols.
• Develop, refine, and oversee deliverables such as study protocols, statistical analysis plans, clinical study reports, project plans, SOPs, etc.
• Ensure rigor, reproducibility, and adherence to good clinical practice (GCP), human subjects protections, and federal regulatory standards.
• Provide direction on study design, endpoints, methodology, and risk mitigation strategies.
• Oversee compliance with federal regulations including FDA, OHRP, NIH policy, HHS human subject protections, and other relevant agency requirements.
• Ensure IRB submissions, amendments, continuing reviews, and reporting obligations (AEs/SAEs, protocol deviations, unanticipated problems) are completed accurately and on time.
• Partner with quality assurance teams to support audits, monitoring visits, corrective action plans, and compliance documentation.
• Prepare and present updates, progress reports, technical summaries, and briefing materials.
• Provide subject matter expert input to stakeholders on emerging data, operational risks, and scientific considerations.
• Collaborate with cross functional departments-clinical operations, data management, biostatistics, regulatory, project management-to ensure integrated and high quality study execution.
• Guide operational teams in translating requirements into actionable project plans, timelines, and workstreams.
• Support the development and enhancement of SOPs, data standards, quality frameworks, and research governance structures.
• Oversee data quality, completeness, and scientific validity across all study activities.
• May lead the interpretation of results, author scientific manuscripts, and contribute to abstracts, posters, and presentations.
• Ensure timely and accurate submission of datasets, reports, publications, and regulatory packages to sponsors.
• Provide leadership and scientific guidance to clinical sites, subcontractors, consortia partners, and external collaborators.
• Participate in investigator meetings, scientific advisory boards, and expert panels.
• Foster collaborative relationships that advance the mission of assigned research programs.
• Ensure continuous protection of human subjects in accordance with federal policy, GCP, and corporate and institutional standards.
• Review safety data, oversee Data and Safety Monitoring Board (DSMB) interactions, and guide risk/benefit assessments.
• Escalates persistent issues and coordinates corrective action plans when needed.
• Selects and evaluates subcontractors and vendors in alignment with project needs and corporate standards.
• Negotiates scopes of work, deliverables, timelines, and pricing in collaboration with contract teams.
• Monitors vendor performance against contractual obligations and project milestones.
• Oversees development and approval of vendor Statements of Work (SOWs) and contract modifications.
• Represents the project in Corporate meetings (e.g., project reviews), with Executive leaders, as applicable.
• Uses key performance metrics to successfully execute the project scope.
• Mentors project staff and supports staff development; may be responsible for the development of new Project Leaders.
• Provide performance related feedback to department managers for project staff.
• Models Emmes culture of integrity, accountability, collaboration, innovation, and perseverance across internal and external teams.
• Promotes and implements relevant corporate initiatives as directed.
• Leads or contributes to the development of operational strategy, budget, and proposal content for new business opportunities, as assigned.
• Develops, maintains, and acquires approval of budgets and statement of work documents and subsequent modifications prior to distribution to clients, as well as approvals for invoices and subagreements.
• Performs other duties as assigned
• Complies with all policies and standards

Qualifications

• Bachelor's Degree Required or
• Master's Degree Preferred or
• PhD Preferred
• 12+ Years + Bachelor's with empirical knowledge of the key accountabilities/duties/responsibilities for the position with a typical tenure of at least 5 years project management experience in a research environment. Required or
• 9 years + Master's with empirical knowledge of the key accountabilities/duties/responsibilities for the position with a typical tenure of at least 5 years project management experience in a research environment. Preferred or
• 6 years + PhD with empirical knowledge of the key accountabilities/duties/responsibilities for the position with a typical tenure of at least 5 years project management experience in a research environment. Preferred
• Project Delivery Track Record: Demonstratable track record of successfully delivering complex/high-priority clinical trials or clinical research projects within the agreed time, quality, and budget. Experience in federally-funded research is preferred. High
• Clinical Research Knowledge: Demonstrated working knowledge of the principles of clinical research management and operations. High
• Problem-Solving: Demonstrated strong problem-solving and analytical skills, combined with sound business and ethical judgment. High
• Communication: Excellent verbal and written communication skills for client, team, and scientific interactions. High
• Leadership & Teamwork: Ability to work proactively and effectively, with creative problem-solving and collaboration skills. Highly motivated with the ability to work independently and as part of a multi-disciplinary team. Ability to supervise, mentor, and support lower-level project leaders and staff.
• Project Management: Strong cross-functional project management and time management skills.
• Therapeutic Expertise (Preferred): Broad understanding of a therapeutic area, clinical trial design, and/or process expertise to influence and execute project decisions.

If you're looking for a career where your work advances global health and where scientific excellence meets real-world impact, join us and be part of something bigger. One Team, One Purpose.