# Local Trial Manager

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Prague-Czech-Republic/Local-Trial-Manager---Sponsor-Dedicated_R1539103?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_7177d40d-f74

## Description

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to work with one single client and to manage clinical research projects in different therapeutic areas.

We currently offer the exciting opportunity to join the FSP team as Local Trial Manager (full-time) in Czech Republic.

Your responsibilities will include:

- Adhering to applicable company’s standard operating procedures (SOPs), work instructions, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc.

- Preparing or contributing to high level budget estimates and detailed budget proposals, ensuring overall contract management, including review and approval of external service provider (ESP) contracts, change orders and ensuring services are delivered per contract.

- Acting as primary company contact for assigned trial at the country level, ensuring local/country team tracks project progress against planned timelines and monitors patient recruitment rate to ensure target enrollment is met across allocated countries.

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

- Contributing to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research targets.

- Delivering competent vendor management at the country level to support the study.

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

- Ensuring trial subject safety by reporting adverse events within required timelines.

- Maintaining inspection readiness by ensuring complete, accurate and timely data and essential documents.

- Working closely with Global Trial Lead and Clinical Project Lead to implement CAPA for audits/inspections or quality-related issues.

- Ensuring accurate finance reporting and trial delivery within budget.

- Keeping the trial in compliance with local regulatory requirements.

Qualifications:

- Master’s or higher-level degree in life science.

- Minimum of 5 years of clinical research experience in the pharmaceutical industry or CRO, plus 1-3 years of local clinical trial management experience.

- Therapeutic area expertise in Oncology or Hematology is preferred.

- Strong working knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

- Fluent language skills in Czech (at least C1 level) and good command of English.

- Strong IT skills in appropriate software and company systems.

- Excellent decision-making and strong financial management skills.

- Flexibility and ability to manage study teams in a virtual environment.

- Willingness to travel occasionally for business meetings.

## Skills

### Required
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH) guidelines
- Czech
- English language
- clinical research
- life science
- Oncology
- Hematology

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Prague-Czech-Republic/Local-Trial-Manager---Sponsor-Dedicated_R1539103?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)