Remote Ppd Clinical Research Jobs in Ridgewood, NJ

In this remote role you will serve as the primary country-level leader for clinical trial delivery, ensuring studies are executed efficiently from start-up through closeout. You will oversee local trial operations, drive performance, and collaborate cross-functionally to deliver high-quality data aligned with regulatory requirements and sponsor expectations.

This role is ideal for a clinical operations professional who thrives in a fast-paced, large matrixed environment and is passionate about improving patient outcomes through clinical research.

Key Responsibilities

Clinical Trial Delivery & Oversight

• Lead end-to-end country-level trial management, from study start-up through database lock and closeout
• Serve as the primary contact for assigned clinical trials within your country
• Ensure delivery of high-quality, compliant data and documentation aligned with ICH-GCP, SOPs, and regulatory standards
• Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target

Site & Stakeholder Management

• Partner with CRA's, Global Project Leads, and cross-functional teams to ensure successful study execution
• Lead site feasibility, selection, and activation processes
• Drive investigator engagement and site performance, including recruitment and retention strategies

Operational Excellence & Compliance

• Monitor study progress through systems and reports; implement corrective and preventive actions (CAPA) when needed
• Ensure inspection readiness through complete and accurate trial documentation (CTMS, eTMF)
• Oversee patient safety reporting (AEs/SAEs) within required timelines

Financial & Vendor Management

• Manage country-level budgets, forecasting, and financial tracking
• Oversee local vendors and site payments, ensuring timely and accurate processing

Regulatory & Quality Assurance

• Coordinate ethics and regulatory submissions/approvals in collaboration with start-up teams
• Ensure compliance with local regulations and global standards (ICH-GCP)

What You Bring

Required Qualifications

• Bachelor's degree in life sciences, healthcare, or related field
• Strong knowledge of ICH-GCP, regulatory requirements, and clinical trial processes
• Excellent communication and stakeholder management skills
• Proficiency in clinical systems (e.g., CTMS, eTMF)
• 3-5+ years of total trial management experience
• Experience managing complex or early-phase trials
• Demonstrated ability to lead cross-functional teams and drive performance

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 athttps://jobs.iqvia.com

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. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.