# 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/So-Paulo-Brazil/Sr-Site-Contracts-Associate--IQVIA-Biotech_R1522475?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_ff3bdb69-087

## Description

IQVIA Biotech is seeking a Sr. Site Contracts Associate in Brazil with 5 years of experience in negotiating clinical site contracts and budget templates.

The successful candidate 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.

Key responsibilities include:

- Developing and coordinating investigator grants and estimates, contracting strategies, and proposal text

- Creating contract language, payment language, and budget templates

- Utilizing and maintaining contracting systems, tools, processes, and training materials

- Collaborating with sponsors, stakeholders, and RSU regions and countries

- Providing specialist legal, operational, and financial contracting support

- Assisting with the creation and review of core scientific, technical, and administrative documentation

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

- Ensuring overall contracting efficiency and adherence to project timelines and financial goals

- Reporting contracting performance metrics and out of scope contracting activities

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

Requirements:

- 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

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

- Strong understanding of regulated clinical trial environment and knowledge of 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

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Sr-Site-Contracts-Associate--IQVIA-Biotech_R1522475?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)