# Local Trial Manager

**Company**: IQVIA
**Location**: Kirkland, Quebec
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Local-Trial-Manager--Sponsor-Dedicated---Responsable-local-e--des-essais-cliniques--ddi-e--au-promoteur_R1576742?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_c19a99ec-37e

## Description

The Local Trial Manager (LTM) provides local management of clinical trials within assigned countries, ensuring studies are conducted in accordance with protocol requirements, applicable regulations, ICH-GCP guidelines, and internal procedures.

The LTM is responsible for overseeing operational study delivery from startup through closeout while partnering with cross-functional stakeholders to ensure quality, timelines, and patient recruitment objectives are achieved.

**Key Responsibilities**

- Lead country-level execution of assigned clinical trials, ensuring milestones, quality metrics, and timelines are met.

- Serve as the primary point of contact for country-specific study operations.

- Support site identification, feasibility assessments, site selection, and activation activities.

- Collaborate with investigators, site staff, and cross-functional teams to drive study performance and enrollment.

- Monitor study progress and proactively identify and mitigate operational risks.

- Ensure compliance with applicable regulatory requirements, GCP guidelines, study protocols, and SOPs.

- Oversee site readiness, site performance, and issue resolution throughout the study lifecycle.

- Partner with study teams to develop and execute recruitment and retention strategies.

- Facilitate study team meetings and communicate study updates, risks, and mitigation plans.

- Support management of vendors, study supplies, budgets, and invoicing activities as applicable.

- Coordinate local regulatory submissions and approvals in partnership with study startup teams.

- Ensure timely and accurate maintenance of study documentation, CTMS, and eTMF records.

- Support audit and inspection readiness activities and help address findings through corrective actions.

- Ensure appropriate reporting and documentation of safety-related information and protocol deviations.

- Contribute to process improvement initiatives and best practice sharing across the organization.

**Qualifications**

- Bachelor's degree in Life Sciences, Healthcare, Nursing, Pharmacy, or a related field preferred.

- Clinical research experience with demonstrated experience managing clinical trial activities.

- Strong knowledge of ICH-GCP, clinical trial regulations, and study conduct requirements.

- Experience working with investigators, clinical sites, and cross-functional study teams.

- Excellent organizational, communication, and stakeholder management skills.

- Ability to manage multiple priorities in a fast-paced, matrixed environment.

- Experience with CTMS, eTMF, and other clinical trial management systems preferred.

- Proficiency with Microsoft Office applications.

- Ability to travel as required.

**Preferred Experience**

- Experience overseeing studies from startup through closeout.

- Experience supporting global or multicountry clinical trials.

- Strong problem-solving skills with the ability to proactively identify and address study risks.

- Demonstrated ability to build effective relationships with internal and external stakeholders.

## Skills

### Required
- ICH-GCP
- clinical trial regulations
- study conduct requirements
- CTMS
- eTMF
- Microsoft Office

### Nice to have
- problem-solving
- relationship building

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Kirkland-Quebec-Canada/Local-Trial-Manager--Sponsor-Dedicated---Responsable-local-e--des-essais-cliniques--ddi-e--au-promoteur_R1576742?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)