Remote Research Assistant I (Clinical Trials)

CPC Clinical Research; United States; Hybrid; USD 27,000 - 30,000; Full time

Benefits offered by this job

Comprehensive benefits package

Matching 401(k) plan

Flexible and remote work schedules

Job summary

CPC Clinical Research is hiring a Research Assistant I to support multiple clinical projects. You will be organized and adaptable, serving as a floating resource to assist in project execution, documentation, and data management across sites and sponsors.

The role requires a GED or HS Diploma (nursing or bachelor’s degree preferred) and at least 1 year in a clinical research setting. Proficiency in MS Office and strong communication are essential.

Qualifications

• Basic knowledge of Good Clinical Practice (GCP) guidelines and applicable FDA and ICH regulations for 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 shift priorities quickly while ensuring accuracy and timely completion of tasks.
• Ability to manage conflicts and resolve problems effectively.

Responsibilities

• Serve as a floating resource to perform a variety of activities in support of project execution and management.
• Assist in preparation of Master Plans, Resource Materials, Source Documentation, Meeting Minutes, and submission to the Trial Master File.
• Assist in training administration and tracking for project-specific training.
• Correspond with investigational sites, CPC staff and sponsors to rectify data queries and collect outstanding documentation.
• Assist in tracking data receipt, entry, upload, reviews and feedback to sites.
• Assist with distribution of study materials to team members, sponsors and sites.
• Assist with query management.
• Assist with User Acceptance Testing (UAT) and manage user access requests.
• Collaborate with team to ensure timely completion of deliverables and issue resolution.
• Participate in CPC meetings as required.
• Adhere to CPC SOPs, GCP guidelines and applicable regulations.
• Serve as a study coordinator for select projects as needed.
• Additional activities as required.

Skills

MS Office

Communication

Attention to detail

Organization

Education

GED or HS Diploma required

Nursing or bachelor’s degree preferred

Tools

MS Excel

MS Word

Job description

CPC Clinical Research is hiring a Research Assistant I to support multiple clinical projects. You will be organized and adaptable, serving as a floating resource to assist in project execution, documentation, and data management across sites and sponsors.

The role requires a GED or HS Diploma (nursing or bachelor’s degree preferred) and at least 1 year in a clinical research setting. Proficiency in MS Office and strong communication are essential.