Research Assistant I

Responsibilities

• Serve as a floating resource to perform a variety of activities in support of the execution and management of projects and programs
• Based on business needs, may provide assistance to the following functional areas: + Research Operations + Community Health + Endpoint and Specialty Services + Site Operations + Data Management + Quality Control + Trial Master File
• Assist in the preparation of Master Plans, Resource Materials, Source Documentation, Meeting Minutes, and submission of documents to the Trial Master File
• Assist in the administration and tracking of project-specific training
• Correspond with investigational sites, CPC staff and sponsors to rectify data queries and collect outstanding documentation
• Assist in tracking receipt, entry, upload, reviews and feedback to investigational sites of endpoint testing
• Assist with the printing, collation and distribution of study materials to project team members, sponsors and sites
• Assist with query management
• Assist with User Acceptance Testing (UAT) and manage user access requests (including user reconciliation)
• Work closely with other team members to ensure timely completion of deliverables and resolution of issues
• Participate in project, program, functional area and general CPC meetings as required
• Adhere to CPC SOPs, Good Clinical Practice guidelines and applicable federal, state and local regulations
• Serve as a study coordinator for select projects as needed
• Additional activities as required

Preferred

• Nursing or bachelor's degree preferred

Benefits

• Comprehensive benefits package (medical, dental, vision, life, STD, LTD etc.)
• Matching 401(k) plan (dollar for dollar up to 4% of your eligible compensation, fully vested immediately)
• 11 paid holidays
• 15 - 25 vacation days based on years of service
• Paid sick time (2.67 hours accrued bi-weekly up to a maximum of 80 hours)
• Flexible and remote work schedules
• Founded in 1989 by the University of Colorado, CPC has two divisions.
• Aurora, Colorado, USA
• https://cpcclinicalresearch.org/
• Distribution of Different Job Fields Receiving Sponsorship
• Represents job field similar to this job
• Engineering and Development
• Trends of Total Sponsorships
• *2026
• (1)
• 2025
• (3)
• 2024
• (12)
• 2023
• (27)
• 2022
• (83)
• 2021
• (18)
• 2020
• Growth Stage
• Recent News
• Morningstar.com
• Rezera Announces Plans to Launch the REVEAL-PAD Multi-Center Study Investigating the Role of Inflammation in Patients with Peripheral Artery Disease

Qualifications

• GED or HS Diploma required
• Minimum of 1 year of experience working in a clinical research setting or commensurate experience
• Basic knowledge of the Good Clinical Practice guidelines and the applicable FDA and ICH regulations for conducting clinical drug trials
• Basic understanding of the drug development process
• Proficiency in MS Office, particularly spreadsheet databases and word-processing
• Good communication and organizational skills
• Great attention to detail
• Ability to work with others in a manner that promotes group effort and achievement
• Ability to shift priorities quickly while ensuring accuracy and timely completion of tasks
• Ability to manage conflicts and resolve problems effectively
• Ability to follow direction to accomplish day-to-day tasks
• Nursing or bachelor's degree preferred
• Minimum of 1 year of experience working in a clinical research setting or commensurate experience.

Required skills

• Clinical Research, Drug Development Process, FDA and ICH Clinical Trial Regulations

Preferred skills

• Nursing or bachelor's degree preferred

Experience

• 1+ years