Site Contract Analyst - IQVIA Biotech

IQVIA; Remote; PLN 102,000 - 273,000; Full time

Job summary

A leading biotechnology firm is seeking a Site Contracts Associate to support clinical development by managing start-up contracting activities. You will develop grant estimates, collaborate with stakeholders, and ensure compliance with project goals. The ideal candidate has a Bachelor's Degree in life sciences and 2-5 years of relevant experience in contract negotiation. Strong communication, technical writing, and organizational skills are essential for this homebased role. This position offers a competitive salary range and opportunities for career growth.

Benefits

Health and welfare benefits

Incentive plans

Bonus potential

Qualifications

• 2 - 5 years relevant experience in contract negotiation.
• Experience with clinical site contracting.
• Understanding of GCP/ICH and regulatory guidelines.

Responsibilities

• Support start-up contracting activities for studies.
• Develop investigator grant estimates for proposals.
• Ensure collaboration with stakeholders and sponsors.

Skills

Contract negotiation

Communication skills

Interpersonal skills

Technical writing

Organizational skills

Education

Bachelor's Degree in life sciences or health care

Tools

Microsoft Office

Job description

Site Contracts Associate

IQVIA Biotech

Poland, Serbia, Spain, Slovakia - 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.

Job Overview

Support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsor’s requirements, including pre-award activities.

Essential Functions

• Develop simple investigator grant estimates and proposal text to support the proposal development process.
• Utilize and maintain contract and budget templates and contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.
• Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
• Provide specialist operational and financial contracting support to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.
• Assist in the creation and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.
• Contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.
• Ensure overall contracting efficiency and adherence to project timelines and financial goals; report contracting performance metrics and out of scope contracting activities as required.
• Comply with contract management and quality standards. Provide administrative and operational support to investigator site contract analysts, managers and directors as required.
• Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.

Qualifications and Skills

• Bachelor's Degree in life sciences or health care
• 2 - 5 years relevant experience, including demonstrable experience acting as a contract negotiator.
• Relevant sponsor or clinical research organization clinical site contracting experience.
• Good negotiating and communication skills.
• Good interpersonal skills and a strong team player.
• Strong technical writing skills.
• Understanding of regulated clinical trial environment and knowledge of drug development process.
• Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
• Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards.
• Good organizational and planning skills.
• Strong knowledge of Microsoft Office and e-mail applications.
• Ability to interpret pricing models and to prepare proposals, bid grids and budgets.
• Good understanding of clinical trial contract management.
• Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.

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 https://jobs.iqvia.com

The potential base pay range for this role, when annualized, is zł102,800.00 - zł272,500.00. 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.

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.

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