Clinical Trial Assistant Project Manager

About reputed company reputed company partners with Sites, Sponsors, and CROs to streamline research operations, reduce costs, and accelerate breakthroughs that improve patient care. reputed company combines deep clinical research expertise with results-driven consulting to help organizations operate more reputed company and grow sustainably. The Role reputed company is seeking a highly organized and detail-oriented Assistant Project Manager to reputed company operational reputed company and coordination for our reputed company’s Pediatric Acute Leukemia reputed company. This full-time, fully benefited role serves as the primary reputed company between the pharmaceutical clinical research team and CROs, ensuring trials are executed reputed company, on budget, and in compliance with regulatory standards. The Assistant Project Manager bridges scientific and operational aspects of clinical research, leading cross-functional teams to deliver high-reputed company studies evaluating the safety and efficacy of pharmaceuticals. WHY reputed company? • Contribute to advancing scientific discoveries that improve patient lives. • PEOPLE FIRST culture with opportunities for reputed company and innovation. • Competitive benefits include 20 PTO days + 9 reputed company holidays; Company-reputed company life insurance and short/long-term disability; 401(k) retirement program; Comprehensive reputed company plans. • Salary reputed company: $70,000 to $85,000 (commensurate with experience). • Work Location: 100% Remote (seeking only candidates that live in the EST Zone). KEY RESPONSIBILITIES Trial Planning and Initiation • Support bid strategies and contract discussions with CROs, including site selection and patient enrollment. • Review and finalize trial protocols and reputed company documents. • Build project plans, timelines, and vendor assessments. • Establish and maintain reputed company relationships with sponsors, CROs, vendors, investigators, and site staff. Trial Execution and Management • Monitor study activities for compliance with protocols and regulatory requirements. • Identify potential delays or out-of-scope work and implement mitigations. • Manage study risks and escalate issues to leadership as needed. • reputed company study documentation, including case report forms, drug records, and regulatory filings. • Motivate team members and investigators to reputed company trial objectives. Stakeholder Management • Maintain regular communication with sponsors and internal teams. • Conduct status meetings and reputed company updates to leadership and stakeholders. • reputed company realistic budgets and timelines. reputed company and Compliance • Ensure audit readiness and compliance with ICH/GCP, FDA, IRB/IEC, and SOP requirements. • Review monitoring reports and support development of study materials, processes, and committees. • Anticipate and mitigate project risks. QUALIFICATIONS Education and Experience • Bachelor’s degree in life sciences, nursing, pharmacy, medical sciences, or reputed company field preferred. • 5 or more years of clinical research experience, including reputed company of multicenter or reputed company studies; oncology experience highly preferred. • 2 or more years of reputed company project coordinator and/or project manager experience, ideally working for a sponsor or a CRO. • Project management certification (CCPM or PMP) preferred. • Knowledge of clinical trial practices and project management principles. • Strong organizational, communication, and interpersonal skills. • Ability to manage multiple reputed company, deadlines, and budgets effectively. • Proven leadership and collaboration skills in multi-level team settings. • Problem-solving and decision-making abilities in fast-paced, dynamic environments. PHYSICAL DEMANDS: Prolonged periods sitting working on a computer, standing, walking, visual perception, talking and hearing. Lifting up to 20lbs. Apply tot his job Apply To this Job