Senior Site Contracts Associate

🔥 3 minutes ago

Apply Now

Find Similar Remote Jobs

Receive Emails For Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 $1G Post-IPO Debt on 2023-05

Healthcare Insurance • Biotechnology • Artificial Intelligence

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Develop complex investigator grant estimates, contracting strategies, and proposal text to support business development. • Create and maintain contract and budget templates, systems, tools, processes, and training materials for complex studies and multi‑protocol programs. • Collaborate closely with sponsors, stakeholders, and RSU regional teams to ensure successful delivery of the project scope and compliance with sponsor requirements. • Provide legal, operational, and financial contracting expertise to support site agreements and facilitate efficient study start-up and maintenance. • Create and review scientific, technical, and administrative documentation required for study initiation. • Assess the contracting landscape and contribute to the analysis and dissemination of contracting intelligence across the company. • Ensure contracting efficiency, adherence to timelines, and achievement of financial targets. • Track and report contracting performance metrics and out-of-scope activities. • Partner with Quality Management to uphold high contract management and quality standards. • Mentor and coach colleagues, delivering training and technical guidance. • Present to clients and professional bodies as needed. • Maintain accurate internal system documentation, including CTMS, trackers, and project plans. • Build and maintain strong relationships with preferred clients, serving as liaison for key accounts when required.

🎯 Requirements

• Bachelor’s degree in a related field (required). • 7+ years of site contracting experience within a sponsor or CRO, including demonstrable experience as an international contract expert. • Strong negotiation and communication skills, with the ability to challenge and influence. • Excellent interpersonal skills and proven success working within matrix teams. • Advanced legal, financial, and technical writing abilities. • Solid understanding of clinical trial regulations, GCP/ICH, and the overall drug development process. • Knowledge of local and global regulatory requirements, SOPs, and corporate standards. • Ability to exercise independent judgment and take calculated risks. • Strong project leadership skills and experience mentoring others. • Excellent planning, organizational, and presentation skills. • Strong proficiency in Microsoft Word, Excel, and other Office tools. • Deep knowledge of clinical trial contract management processes. • Proven experience leveraging metrics to establish timelines and deliverables. • Ability to initiate and grow programs across departments to drive organizational impact.

🏖️ Benefits

• Opportunity to work on global, high‑complexity clinical programs. • A collaborative, supportive, and growth‑oriented environment. • The chance to influence key clients and shape contracting strategy at scale. • Career progression and professional development opportunities.