Clinical Research Associate, Sponsor Dedicated Clinical Research Associate, Sponsor Dedicated 5 days ago Be among the first 25 applicants Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for IQVIA. To be eligible for this position, you must reside in the same country where the job is located. Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. Collaborate and liaise with study team members for project execution support as appropriate. If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. Qualifications Bachelor's Degree Degree in scientific discipline or health care preferred. Req Requires at least 2 years of year of on-site monitoring experience. Req Equivalent combination of education, training and experience may be accepted in lieu of degree. Req Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Good therapeutic and protocol knowledge as provided in company training. Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). Written and verbal communication skills including good command of English language. Organizational and problem-solving skills. Effective time and financial management skills. Ability to establish and maintain effective working relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. The potential base pay range for this role, when annualized, is $71,900.00 - $189,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. EEO Minorities/Females/Protected Veterans/Disabled If you have questions about this posting, please contact support@lensa.com Seniority level Seniority level Entry level Employment type Employment type Part-time Job function Job function Research, Analyst, and Information Technology Industries Internet Publishing Referrals increase your chances of interviewing at Lensa by 2x Sign in to set job alerts for “Clinical Research Associate” roles. Washington, DC $42,702.40-$71,156.80 1 week ago Washington, DC $42,702.40-$71,156.80 2 weeks ago Washington, DC $42,702.40-$71,156.80 2 weeks ago Silver Spring, MD $42,702.40-$71,156.80 2 weeks ago Washington, DC $50,252.80-$83,761.60 5 days ago Washington, DC $50,252.80-$83,761.60 2 weeks ago Gaithersburg, MD $59,100.00-$87,900.00 2 months ago Washington, DC $50,252.80-$83,761.60 5 days ago Washington, DC $50,252.80-$83,761.60 1 week ago Washington, DC $50,252.80-$83,761.60 2 weeks ago Washington, DC $50,252.80-$83,761.60 2 weeks ago Silver Spring, MD $50,252.80-$83,761.60 2 weeks ago Rockville, MD $90,000.00-$120,000.00 1 month ago Gaithersburg, MD $50,000.00-$65,000.00 1 week ago Research Assistant I - Suicide CRP Initiative Clinical Research Coordinator I- Arlington, VA Junior Scientist (Human Research Protections) Washington, DC $60,000.00-$85,000.00 2 days ago Clinical Research Associate (DMD/neuromuscular) Washington, DC $36,400.00-$47,320.00 2 weeks ago Washington, DC $36,400.00-$47,320.00 2 weeks ago Washington DC-Baltimore Area $44,000.00-$54,000.00 4 days ago Washington, DC $61,560.00-$76,950.00 1 week ago Bethesda, MD $49,000.00-$81,000.00 2 weeks ago We’re unlocking community knowledge in a new way. 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