Clinical Research Associate II

Summary

Join Precision Medicine Group as an In-house CRA II, providing comprehensive support to clinical research study sites and teams. You will adhere to GCP and regulatory guidelines, acting as a key point of contact for study sites. Responsibilities include assisting with investigator recruitment, site file preparation, document management, data entry, and communication with study personnel. The role requires a Bachelor's degree, 2+ years of relevant experience, proficiency in Microsoft Office, and strong communication skills. Preferred qualifications include solid clinical research experience and excellent organizational skills. This position offers a competitive salary, annual bonus, health insurance, retirement benefits, life and disability insurance, parental leave, and paid time off.

Requirements

• Bachelor's degree / international equivalent or equivalent combination of education and experience ideally in a business, scientific or healthcare discipline
• Minimum of 2 years of relevant experience
• High in proficiency in the Microsoft Office package of programs (Outlook, Word, Excel, and PowerPoint)
• Customer service demeanor; demonstrate flexibility and teamwork
• Ability to focus on detail for extended periods of time, high attention to accuracy
• Fluency in English communication, verbally and in writing
• Working knowledge of the drug development process
• Ability to travel as needed

Responsibilities

• Assist with the investigator recruitment activities utilizing phone scripts, questionnaires, study site materials and other tools for use in evaluating investigative sites
• May assist in identifying study sites by performing site feasibility and recruitment tasks, e.g., completing, disseminating, and reviewing responses to site recruitment questionnaires
• Schedules internal and external meetings as required
• Prepares Investigator Site Files including distribution to study sites (electronically or physically), coordination with shipping vendor, if required
• Performs ongoing essential document collection and review, maintenance, and close-out activities, organizing and maintaining site level data in the trial master file (TMF) under general supervision ensuring that sponsor and investigator obligations are being met and are compliant with ICH/GCP guidelines and applicable local regulations
• Assist with sets up and maintains site-related data in applicable clinical systems according to procedures and guidelines. Utilizes the Clinical Trial Management System (CTMS) to ensure milestones and activities are accurately tracked
• Acts as site contact/liaison for study and site management issues including addressing questions, assists with managing study supplies, and may support offsite central monitoring activities. Escalates issues and risks as needed
• Ensures timely and complete data entry by site in EDC or any other system that requires data entry
• Sends email blasts/newsletter, updates, and updated study core documents to study site personnel
• Assists in providing logistics support in samples management and tracking, where applicable and in study supply management
• Supports investigators and investigative staff in fulfilling obligations regarding local submissions according to local regulatory and Institution Review Board (IRB)/Independent Ethics Committee (IEC) requirements
• Assists in data review inclusive of site level data review, resolutions provided by sites to queries, facilitates database closure and freezing procedures as per study plans
• Assist with study tracking via the CTMS, Study specific trackers or Sponsor designated system to ensure that the study reporting is current, accurate and complete
• Documents site and Sponsor contact and study interactions in a timely and professional manner
• Assist in remote review of the electronical Investigator Site File, where applicable
• Assists with Investigational Product accountability, where applicable
• Consults with project team members regarding study site issues
• Provides quality review of the amended site level informed consent template
• Follows up with sites for trial invoices and ensures the CTMS is accurately updated to allow the timely processing of Investigator Payments
• May attend site visits as needed, supporting the CRA to ensure sponsor and investigator obligations related to the study documentation are being met and are compliant with applicable regulatory requirements and guidelines
• May serve as an Independent Essential Document Reviewer post-SIV
• Supports on-site visits activities if needed
• May mentor an In-house CRA Trainee (New Graduate Level)
• Performs other duties as assigned by management
• Performs all tasks in accordance with applicable guidelines, (e.g., ICH-GCP), company and sponsor SOPs, project plan, study-specific processes, local regulatory requirements

Preferred Qualifications

• Solid experience in clinical research or related experience
• Excellent organizational skills
• Ability to work efficiently in a remote work environment

Benefits

• Discretionary annual bonus
• Health insurance
• Retirement savings benefits
• Life insurance
• Disability benefits
• Parental leave
• Paid time off for sick leave and vacation