# Sr. Site Contracts Associate

**Company**: IQVIA Biotech
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/Sr-Site-Contracts-Associate--IQVIA-Biotech_R1533697?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_2f19cf1a-53f

## Description

IQVIA Biotech is seeking a Sr. Site Contracts Associate with 3-5 years of experience in negotiating clinical site contracts and budget templates. As a Sr. Site Contracts Associate, you will develop the global contracting strategy and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs.

**Essential Functions:**

- Develop and coordinate investigator grants and estimates, contracting strategies, and proposal text to support the proposal development process.

- Create contract language, payment language, and budget templates as required.

- Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs.

- Ensure collaboration 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 legal, operational, and financial contracting support to the Study Teams.

- Assist with the creation and/or review of core scientific, technical, and administrative documentation.

- Contribute to the collection, interpretation, analysis, and dissemination of accurate contracting intelligence.

- Ensure overall contracting efficiency and adherence to project timelines and financial goals.

- Report contracting performance metrics and out of scope contracting activities.

- Work with Quality Management to ensure appropriate contract management and quality standards.

**Qualifications:**

- Bachelor's Degree in a related field.

- 3-5 years of relevant sponsor or clinical research organization clinical site contracting experience.

- Good negotiating and communication skills with the ability to challenge.

- Strong legal, financial, and/or technical writing skills.

- Strong understanding of the regulated clinical trial environment and knowledge of the drug development process.

- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.

## Skills

### Required
- clinical trial contract management
- GCP/ICH
- regulatory guidelines
- negotiation
- communication
- legal writing
- financial writing
- technical writing

### Nice to have
- Grant Plan

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