Senior Site Contracts Associate, IQVIA Biotech

IQVIA Biotech

Poland - Homebased

IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure collaborative culture and deep therapeutic expertise allow us to deliver tailored solutions that help bring innovative treatments to patients faster.

Overview

We are seeking an experienced Senior Site Contracts Lead / Contract Strategy Manager to manage contract strategy and oversee all startup contracting activities for selected this role you will support complex studies and multiprotocol programs ensuring high-quality delivery and operational excellence. This position may also include linemanagement responsibilities.

If you are a strategic thinker with strong expertise in international clinical trial contracting wed love to speak with you.

Key Responsibilities

• 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 multiprotocol 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.

Qualifications & Experience

• Bachelors 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.

• Equivalent combinations of education training and experience will be considered.

• 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.

What We Offer

• Opportunity to work on global highcomplexity clinical programs.

• A collaborative supportive and growthoriented environment.

• The chance to influence key clients and shape contracting strategy at scale.

• Career progression and professional development opportunities.

If youre passionate about driving excellence in clinical trial contracting and want to make an impact across global programs we encourage you to apply!