Research Assistant II

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
Endpoint and Specialty Services
Site Operations
Data Management
Quality Control
Trial Master File
Work closely with other team members to ensure timely completion of deliverables and resolution of issues.
Perform a variety of general administrative tasks such as filing, copying, and preparation of shipments for assigned projects.
Upload essential documents into eTMF system.
Perform quality control reviews of project-specific documentation and support submission of documents to the Trial Master File.
Perform ALCOA+ checks of documents uploaded into eTMF system.
Participate in project, program, functional area and general CPC meetings as required.
Assist in the preparation of Master Plans, Resource Materials, Source Documentation, Meeting Minutes, and submission of documents to the Trial Master File.
Coordinate and track receipt of project supplies to study sites
Assist in tracking receipt, entry, upload, reviews and feedback to investigational sites of endpoint testing.
Assist in the development, administration, and tracking of project specific training.
Manage email reconciliation and export at study close-out.
Collect and review investigational site documentation and process as directed.
Correspond with investigational sites, CPC staff and sponsors to rectify data queries and collect outstanding documentation.
Serve as one of the primary points of contact for investigational sites.
Perform query management, report generation, and data reconciliation tasks.
Assist with User Acceptance Testing (UAT)
Manage user access requests (including user reconciliation).
Perform general data review of study data in EDCs
Qualifications:
GED or HS Diploma required. Nursing or bachelor’s degree preferred.
Minimum of 1 years of experience working in a clinical research (or similar) setting. Higher degree may be considered in lieu of experience.
Demonstrated ability to complete core tasks with minimal direction, while reliably escalating for guidance on less routine assignments.
Thorough knowledge of the Good Clinical Practice guidelines and the applicable FDA and ICH regulations for conducting clinical drug trials.
Good understanding of the drug development process.
Proficiency in MS Office, particularly spreadsheet databases and word-processing.
Excellent 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 discern priorities and obtain direction to accomplish day-to-day tasks.
Posting deadline: This posting will remain open until filled. For best consideration, please apply by September 29, 2026.
CPC offers:
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
An Equal Opportunity Employer
CPC is dedicated to the principles of equal employment opportunity (EEO). CPC prohibits unlawful discrimination against applicants or employees on the basis of age 40 and over, race (including traits historically associated with race, such as hair texture and length, protective hairstyles), sex, sexual orientation, gender identity, gender expression, color, religion, creed, national origin, ancestry, disability, military status, genetic information, marital status, or any other status protected by applicable state or local law. It is our intention that all qualified applicants are given equal opportunity and that selection decisions be based on job-related factors.
Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act (ADA) and certain state or local laws. If you need assistance, please email our Human Resources team at careers@cpcmed.org.

Employment type
Full-Time

Work arrangement
Yes