Site Operations Specialist

Science 37; Morrisville (NC); On-site; USD 50,000 - 70,000; Full time

Job summary

Science 37 is seeking a Site Operations Specialist in North Carolina to enable trial start‑ups, logistics, and data management. You’ll support Site Operations Managers and cross‑functional teams while maintaining study trackers and essential documents.

The role emphasizes coordinating visit schedules, budgets, and recordkeeping, with an emphasis on accuracy, compliance, and professional collaboration across sponsors and sites.

Qualifications

• Associate’s or Bachelor’s degree preferred.
• 1+ years of clinical research or administrative experience (sponsor, CRO, or site).
• Strong organizational and multitasking skills with high attention to detail.
• Proficiency in Microsoft Office Suite and familiarity with clinical trial systems.
• Excellent written and verbal communication skills.
• Ability to work both independently and collaboratively in a fast-paced environment.
• Commitment to maintaining confidentiality and compliance with regulatory standards.

Responsibilities

• Draft agendas and minutes for internal and external Study Team meetings.
• Maintain key study trackers and related documentation (e.g., contacts, logs, budgets, contracts).
• Assist in Investigator Site File updates and e-filing of documents.
• Track study start-up and close-out documentation.
• Coordinate across teams to track plans and timelines.
• Support scheduling of participant visits and site logistics.
• Assist with vendor management and data entry across systems.
• Ensure accurate filing and archiving of essential trial documents.

Skills

Clinical research

GCP knowledge

Data entry

Documentation management

Communication skills

Attention to detail

Organizational skills

Cross-functional teamwork

Education

Bachelor's degree

Associate’s degree

Tools

IWRS

CTMS

eTMF

MS Office

Google Apps

Job description

Science 37’s mission is to accelerate clinical research by enabling universal trial access for patients. Through our solutions; Direct-to- Patient Site and Patient Recruitment, we accelerate enrollment by expanding the reach of clinical trials to patients beyond the traditional site and rigorously qualifying patients prior to referring them to a traditional site. Our solutions are powered by a proprietary technology stack with in‑house medical and operational experts that enhance quality through standardized workflows and best‑in‑class study orchestration.

The Site Operations Specialist plays a critical role in overall site enablement and the successful execution of clinical trials. This position supports a wide range of functions essential to the start‑up, implementation, and conduct of Phase I, II, III, and IV clinical studies. Working cross‑functionally, the Site Operations Specialist provides operational support to Site Operations Managers, Logistics Managers, Medical Record Supervisors, Recruitment Operations Managers, Scheduling Logistics Managers, Clinical Project Managers, and Clinical Research Coordinators.

Key responsibilities include supporting study start‑up activities, maintaining and tracking clinical budget data, assisting with medical record acquisition and follow‑up, coordinating logistics and visit scheduling, and contributing to the upkeep of clinical dashboards, metrics, and multi‑system administration. This role is also responsible for data entry and ensuring accurate tracking and filing of essential documents within the Investigator Site File.

As a foundational member of the clinical operations team, the Site Operations Specialist ensures operational readiness and efficiency across departments, making this role indispensable to the broader success of site activation and trial delivery.

DUTIES AND RESPONSIBILITIES

Duties include but are not limited to:

• Drafts agendas and minutes for internal and/or external Study Team meetings
• Responsible for maintaining key study trackers, including but not limited toStudy Contacts Lists, Study Question and Answer Logs, Site Budgets Log, clinical site contracts tracker, medical record status, and participant trackers.
• Assists in creating and update of Investigator Site Files, including any e‑filling or printing of required study documents
• Tracks required documentation for study start‑up and close out
• Assists in tracking and finalizing study plans as requested by study team
• Assists in vendor management, including the efficient use of web tools such as IWRS, IRB web portals and central lab web portals to track the progress of studies and to ensure the studies are running smoothly
• Reviews data queries for accuracy and consistency prior to distribution to clinical sites
• Maintains complete and accurate clinical study documentation
• Represents Science 37 in a professional manner; establishes and maintains good relationships with investigators and all other study personnel
• Assists with coordinating Investigator Meeting attendees and items with Sponsor(s)
• Performs additional study related functions as required, e.g., preparation of and tracking payments to investigators, and participation in clinical project planning
• Supports the maintenance of the clinical dashboard
• Links CRFs to any Data Clarifications Forms/ information (if paper)
• Files/ uploads documents after scanning
• Attend Staff Meeting as needed
• Supports clinical documents filing
• Supports Logistics
• Support Medical Record Acquisition/follow up
• Supports front desk office staff as needed
• Supports scheduling of participant visits
• Other tasks as assigned

Technical Skills:

• Clinical Research Knowledge
• Understanding of clinical trial phases (I–IV), GCP (Good Clinical Practice), and basic regulatory requirements
• Familiarity with clinical trial documents and workflows (e.g., ISF, CRFs, ICFs)
• Data and Document Management
• Experience with eTMF systems and document control
• Ability to manage and organize large volumes of trial documentation
• Skilled in accurate data entry and quality control
• Clinical Systems Proficiency
• Comfortable using CTMS, IWRS/IRT systems, and vendor portals (e.g., IRB, central lab) a plus
• Proficient in Microsoft Office and Google Applications
• Experience with dashboards or reporting tools is a plus
• Scheduling and Logistics Coordination
• Experience supporting scheduling of patient visits and managing site logistics is a plus
• Ability to coordinate across multiple teams and timelines

Soft Skills:

• Attention to Detail
• Ability to manage complex documentation with accuracy and consistency
• Vigilant in identifying errors or missing information
• Organizational Skills
• Excellent time management with the ability to prioritize multiple tasks
• Structured and systematic in tracking deadlines and deliverables
• Communication Skills
• Strong written and verbal communication for clear documentation and correspondence
• Professional demeanor when interacting with sponsors, sites, and internal teams
• Works effectively within cross‑functional teams
• Willing to assist in multiple areas to meet site and study needs
• Adaptability and Initiative
• Able to pivot between tasks and handle shifting priorities in a dynamic environment
• Proactive in identifying ways to improve operational efficiency

Core Competencies:

• Accountability: Takes ownership of assigned tasks and delivers high‑quality work with minimal oversight
• Problem‑Solving: Can troubleshoot basic operational issues and escalate appropriately
• Confidentiality and Integrity: Handles sensitive patient and trial data with discretion
• Customer Service Orientation: Maintains professionalism and responsiveness in support of clinical sites and participants
• Process‑Oriented Mindset: Follows established protocols while contributing to continuous improvement efforts

QUALIFICATIONS & SKILLS

Qualifications

The following qualifications are preferred/or equivalent applicable experience:

• Associate’s or Bachelor’s degree in a life sciences, healthcare, or related field preferred
• 1+ years of clinical research or administrative experience, preferably in a sponsor, CRO, or site setting
• Strong organizational and multitasking skills with high attention to detail
• Proficiency in Microsoft Office Suite and familiarity with clinical trial systems
• Excellent written and verbal communication skills
• Ability to work both independently and collaboratively in a fast‑paced environment
• Commitment to maintaining confidentiality and compliance with regulatory standards

Capabilities

• Required to be in the North Carolina office 5 days a week for 6 months, following approval, may move to rotation of 3 days a week in office.
• Up to 10% travel, as needed, for study visits, training, project team meetings, client presentations and other professional meetings/conferences as needed
• Ability to communicate in English (both verbal and written); fluency in other languages is a plus.
• May require extended or unusual work hours based on research requirements and business needs.

DIRECT REPORTS

BENEFITS

At Science 37, our focus is to provide you with a comprehensive and competitive total reward package that supports you at all stages of your career - both now and into the future. Our success depends on the knowledge, capabilities, and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work that adds to your professional development.

Science 37 is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.

Science 37 values the well‑being of its employees and aims to provide team members with everything they need to succeed.