Clinical Research Associate (Part time Contractor)

Job Responsibilities Works on assigned studies to ensure that human subject protection is maintained, Good Clinical Practice (GCP), and applicable regulations are followed. Coordinates and manages clinical site monitoring responsibilities for assigned studies in accordance with contractual agreements, SOPs, and applicable regulatory guidelines. May conduct on-site and remote site qualification, site initiation, interim, and site close-out monitoring visits. Serve as primary point of contact for site questions relating to study enrollment, conduct, and close‑out issues: liaise with appropriate study team members as needed. Communicates through verbal and written communication with site investigator and project team overall site performance, trends, deficiencies, and concerns. Supports study start‑up activities such as tracking and performing quality review of study documents, completing, and distributing site activation letters, etc. Performs study‑related training. Manages the development and maintenance of study documents, processes and systems as assigned. Ensures quality and completeness of central and site master files. Tracks and maintains required study documents, performs quality control review, manages renewals. Tracks study site and overall study metrics including but not limited to enrollment, deviations, adverse events, trial master file maintenance. Attends internal and external meetings as required. Provides all job‑related progress reports and visit documentation as required. May support safety activities such as narrative writing, managing the CEC/DSMB, etc. OUS: Prepares and coordinates submissions to regulatory authorities. May perform other activities as assigned. Qualifications & Technical Competencies Fluency in English and local language, if different, required. Higher education degree or equivalent education, training, and experience. Preferred 2 years clinical trial experience. Preferred monitoring experience. Able to work independently once trained. Good verbal and written communication skills. Strong organizational skills. Basic computer proficiency. Understanding of clinical research processes and regulations. Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) Certification preferred but not required. Working Conditions Up to 20% travel for In‑House Clinical Research Associates; up to 80% travel for Field Clinical Research Associates. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear, frequently required to stand, walk, sit, use hands to finger, handle, or feel and reach with hands and arms, and must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, depth perception, and ability to adjust focus. Extensive use of a computer keyboard. The compensation grade range for this position is: - Please Note: Individual base pay depends on various factors, in addition to primary work location, such as complexity and responsibility of role, job duties/requirements, and relevant experience and skills. Equal Employment Opportunity NAMSA is an equal employment opportunity company. NAMSA participates in pre‑employment background and drug screen processes aligned to local, state and federal laws. #J-18808-Ljbffr North American Science Associates, Inc.