Mastech Digital provides digital and mainstream technology staff as well as Digital Transformation Services for all American Corporations. We are currently seeking a Clinical Trial Assistant for our client in the Health Technology domain. We value our professionals, providing comprehensive benefits and the opportunity for growth. This is a Contract position, and the client is looking for someone to start immediately. Duration: 12+ Months Contract Location: San Diego, CA (Onsite) Role: Clinical Trial Assistant Primary Skills: Systems Analysis Role Description: The Clinical Trial Assistant must have at least 2+ years of experience. Qualifications: - Technology Requirements - Microsoft Word, Excel, PowerPoint, Outlook, Teams, Adobe Acrobat, Sample Management Systems (i.e., Freezerworks) - Perform sample management activities, such as shipping/receiving clinical samples, scanning clinical samples into inventory, organizing freezer space, assisting clinical study team with tasks such as performing inventory of study supplies, shipping/receiving samples and/or supplies, filing documents in the Trial Master File, following written and oral instructions from study team, regularly checking e-mail - Preferred background/prior work experience is Laboratory and/or science background, prior work experience as a CTA or at a Sponsor/CRO - Priority soft skills - Attention to detail, communication, organization, adaptability Responsibilities: - The Clinical Trial Assistant (CTA) supports Clinical Operations personnel with preparation, planning, execution, and close-out of clinical studies - Assists Clinical Research Associates (CRAs) and Clinical Trial Leads (CTLs) with collection, review and tracking of essential study documents - Files essential documents in Trial Master Files per instructions, performs quality control checks on documents and file structure - Creates Investigator Site Binders for study sites and assists with development of written site instructions - Orders, tracks, ships clinical study equipment and supplies, builds study specimen collection kits - Manages clinical study samples i.e., receives, stores, ships, frozen human samples; documents sample management in electronic Lab Information Management System (LIMS) - Maintains tracker tools to support study (e.g., trial master file index, spreadsheets to track collection kits, samples, supplies) - Communicates with external vendor/site personnel via phone and email - Prepares for and participates in clinical study project team trainings and meetings Educational Requirements: - Associates Degree or higher Required Skills: - Able to follow written and verbal instructions - Able to write clear and effective memos and instructions - Low-intermediate level word processing, experience using computers, able to use Microsoft Office, Adobe - Familiarity with completion of electronic forms - Effective time management and organizational skills - Accuracy and attention to detail - Basic knowledge of clinical trials Education: Associates Degree or higher/Bachelors degree in Computer Science, Electrical/Electronic Engineering, Information Technology or another related field or Equivalent Experience: Minimum 2+ years of experience Relocation: This position will not cover relocation expenses Travel: No Local Preferred: Yes Note: Must be able to work on a W2 basis (No C2C) Recruiter Name: Srinivas Rao Recruiter Phone: Equal Employment Opportunity
