Research Assistant I

CPC Clinical Research

3d•$19 - $22

About The Position

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, and Trial Master File. Work closely with other team members to ensure timely completion of deliverables and resolution of issues.

Requirements

GED or HS Diploma required.
Minimum 1 year of professional experience (clinical research experience preferred). Higher degree may be considered in lieu of experience.
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.

Nice To Haves

Nursing or bachelor’s degree preferred.

Responsibilities

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.
Assist in sending project supplies to study sites and tracking receipt of those supplies.
Assist in tracking receipt, entry, upload, reviews and feedback to investigational sites of endpoint testing.
Assist with query management.
Serve as a study coordinator for select projects as needed.
Assist with user access requests (including user reconciliation).
Perform general data review of study data in EDCs.
Additional activities as required.