Project Delivery Associate - OptymEdge

Emmes Global•Rockville, MD

10d•Remote

About The Position

Project Delivery Associate - OptymEdge Location: CA Remote & US Remote OptymEdge, (part of the Emmes Group), develops proven solutions for training and certification of Visual Function Examiners and Visual Acuity Rooms. OptymEdge partners with study teams to provide visual function certification that ensures a high level of quality and consistency for ophthalmic clinical trial data. OptymEdge is the largest and longest-standing certification organization in the industry. We pioneered visual acuity certification from conception. Our services have grown to be synonymous with providing the highest level of quality and standardization of clinical trial data. Over 2,500 sites certified worldwide, since 1995 Phase I through post-marketing experience across anterior segment and retina trials Clinical Ophthalmology, Optometry, and clinical trial expertise Primary Purpose The Project Delivery Associate (PDA) supports the successful delivery of clinical studies within a technology-enabled clinical research environment. Working within defined digital workflows and under close guidance from senior team members, the PDA executes assigned activities that support data accuracy, documentation completeness, and timely delivery. The PDA is clinical site-facing and operational in nature, focused on learning core certification processes, understanding regulated workflows, and developing foundational delivery skills. The PDA contributes to team efficiency through consistent execution, attention to detail, and effective use of systems, forming the baseline for progression into more complex and independent delivery roles.

Requirements

2 years of relevant experience in an administrative, operational, clinical, or technology-supported environment.
Internship, placement, or academic experience in clinical research, healthcare, life sciences, or technology-enabled operations may be considered.
Basic proficiency with Microsoft Office applications, particularly MS Word; exposure to databases or document management systems preferred.
Strong organizational and time-management skills, with the ability to follow defined, technology-enabled processes.
High attention to detail and ability to manage multiple tasks with guidance and oversight from more senior team members.
Clear written and verbal communication skills
Interest in clinical trials, healthcare, or life sciences; ophthalmology experience preferred but not required.
Willingness and ability to learn new systems, tools, and digital workflows in a regulated environment.

Responsibilities

Supports project-specific certification activities under the direction of the Project Delivery Manager (PDM) following established digital workflows.
Performs certification data review, validation and maintenance within electronic systems, ensuring accuracy, completeness and traceability.
Assists in tracking project deadlines, deliverables and milestones for assigned workstreams using electronic tracking tools and templates
Maintains study documentation within electronic systems, ensuring audit readiness and adherence to documentation standards.
Performs basic quality checks by identifying inconsistencies, missing data or deviations from defined workflows and escalating appropriately.
Supports coordination of conference calls, virtual meetings, and routine communications.
Formats, tracks, and distributes technical and non-technical reports using standardized templates and tools.
Supports the PDM in preparation of study start-up documentation and management of training requirements.
Escalates issues, questions, or risks to the PDM or senior team members in a timely manner.
Develops working knowledge of internal platforms and digital tools used across certification, data capture, and imaging workflows.
Participates in team meetings and training sessions to build understanding of systems, processes and clinical trial delivery