# Clinical Trial Manager – Sponsor Dedicated

**Company**: IQVIA
**Location**: São Paulo, Brazil
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Clinical-Trial-Manager---Sponsor-Dedicated_R1556631?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_7d88c8b6-9c9

## Description

We are seeking a Clinical Trial Manager – Sponsor Dedicated to provide management of a clinical trial(s) at a local level. As a Clinical Trial Manager, you will be responsible for the operational oversight of assigned project(s) at the local level for end-to-end project management from start-up through to closeout activities.

**Responsibilities:**

- Adhere to applicable Sponsor SOPs, WIs, policies, codes of Good Clinical Practice (GCP), and local regulatory requirements.

- Prepare or contribute to high-level budget estimates and detailed budget proposals, and ensure overall contract management.

- Act as primary company contact for assigned trials at the country level, ensuring local/country teams track project progress and monitor patient recruitment rates.

- Drive study compliance by maintaining and updating trial management systems, using study tools and management reports to analyze trial progress.

- Contribute to site-level recruitment strategies and contingency planning, and participate in preparation for and conduct of Health Authority (HA) inspections and internal Quality Assurance audits.

- Contribute to patient understanding of protocol and patient safety by reviewing country-specific informed consent forms.

**Requirements:**

- BA/BS degree in a health or science-related field.

- Minimum of 2 years of local/regional trial management experience in the pharmaceutical industry or CRO, and previous experience as a Clinical Research Associate.

- Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols, and associated protocol-specific procedures.

- Strong IT skills in appropriate software and company systems.

- Excellent decision-making and financial management skills.

- Proficiency in speaking and writing the country language and English.

## Skills

### Required
- ICH-GCP
- clinical trial management
- budget management
- contract management
- Good Clinical Practice

### Nice to have
- therapeutic area expertise
- local laws and regulations
- study tools and management reports

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Clinical-Trial-Manager---Sponsor-Dedicated_R1556631?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)