Emmes · 12 hours ago
Associate Global Project Manager
United States
Full-time
Remote
Mid Level
4+ years expEmmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. The Associate Global Project Manager is responsible for the successful delivery of Biopharmaceutical projects, ensuring effective project delivery in agreement with contracted timelines and budgets while maintaining client satisfaction through relationship management.
BiopharmaBiotechnologyClinical TrialsHealth CareMedical
Responsibilities
May serve as a lead for project bids and multi trial initiatives
Ensures that deliverables for assigned project(s) are completed according to the contract budget, schedule, and quality standards. Manages projects in all areas of performance
Develops successful working relationships with clients, executive management, and project staff. Collaborates with stakeholders to manage project issues, proactively identify and mitigate risks and drive milestone achievement
May serve as the primary point of contact for assigned biopharma clients. Demonstrates proficiency in knowledge and understanding of client needs
Tracks project deliverables against contract using Emmes’ tools. Prepares/presents study metrics to maintain transparency for internal/external stakeholders. Monitors trends and drives changes to the plan as needed; identifies risks to delivery and supports development of mitigation plans with the project team
Ensures adherence to quality control expectations and milestone timelines for delivery of contractually required reports and deliverables
Manages project resources (i.e., budget, personnel, and subcontracts)
Identifies and manages changes to scope and requests for out-of-scope activities. Collaborates with Business Development, Contracts Department, and executive management to ensure timely execution of contract amendments/change orders. Prospectively manages client expectations
May support bid defense meeting presentations in collaboration with Business Development for assigned clients
Develops study management plans in collaboration with core project team members
Identifies and documents lessons learned from study successes and challenges to promote development of best practices
Models and propagates Emmes’ commitment to a culture of quality in all aspects of our deliverables, utilizing a solution-based, science-driven, value-added approach in collaborating with clients
Performs other duties as assigned
Qualification
Required
Bachelor's degree in a scientific discipline
Minimum of 4 years demonstrating scientific principles appropriate in managing a clinical research portfolio
Minimum of 1 year in a pharmaceutical and/or CRO setting, serving in a Project Manager or equivalent position
Demonstrable track-record of success delivering clinical trials within agreed time, quality and cost
Demonstrated experience in developing and fostering client and internal relationships
Understanding of ICH GCP and applicable global regulatory regulations and guidelines
Skilled in MS Office Suite of products and working knowledge of Clinical Trial Management Systems, electronic Trial Master File, and electronic Data Capture systems and solutions
Demonstrated experience in managing diverse staff and leading successful teams
Strong verbal and written communication skills
Benefits
Flexible Approved Time Off
Tuition Reimbursement
401k Retirement Plan
Work From Home Anywhere in the US
Maternal/Paternal Leave
Casual Dress Code & Work Environment
Company
Emmes
Emmes is a contract research organization that offers clinical research services for public health and biopharmaceutical innovation.
1001-5000 employees
Funding
Current Stage
Late StageTotal Funding
unknownKey Investors
Behrman Capital
2022-06-21Acquired
2019-03-04Private Equity
Leadership Team
Peter Ronco
Chief Executive Officer
Recent News
2025-09-20
2025-01-18
2024-12-10
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