# Senior Local Operations Manager - HemOnc

**Company**: ICON Strategic Solutions
**Location**: Blue Bell
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Clinical-Trial-Manager_JR163431-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_5d57bfae-bf7

## Description

As a Senior Local Operations Manager - HemOnc at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

The Senior LOM role is a site-aligned E2E partner to streamline communication across cross-functional stakeholders throughout trial lifecycles.

Key responsibilities:

- Serve as the primary point of communication for sites, facilitating internal client teaming to drive issue resolution.

- Intimately understand the site operational model and own relationships with critical site stakeholders to provide a voice for the site to the client's teams.

- Contribute to quality Site Selection through participation in site feasibility, ensuring consistent conduct of site qualification visits, and appropriate follow-up of site qualification visit reports and country feasibility reports.

- Ensure local/country teams meet recruitment targets with high-quality data on time and within study budget.

- Act as the primary company contact for assigned trial sites, engaging with Investigators and Site Staff throughout the life of the trial.

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

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

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

- Ensure high standards for study monitoring by conducting quality local trial team meetings and facilitating SM training when needed.

- Contribute to patient understanding of the protocol and patient safety by preparing country-specific informed consent.

- Ensure trial subject safety by reporting AEs/SAEs/PQCs within required reporting timelines.

- Ensure Inspection readiness by maintaining complete, accurate, and timely data and essential documents in systems utilised for trial management.

- Accountable for ensuring quality data is provided by the site and queries are resolved within expected timelines.

Requirements:

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

- 3-5+ years of trial end-to-end management experience.

- Start-up & Database Locks/Cleaning experience preferred.

- HemOnc experience required.

- 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.

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

Rewards & Benefits:

- Competitive base salary and performance-related incentives.

- Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.

- Retirement and pension plans.

- Life assurance and disability coverage.

- Employee assistance programmes and wellbeing resources.

- Learning and development opportunities through structured training and career pathways.

## Skills

### Required
- ICH-GCP
- trial management
- HemOnc
- communication
- vendor management

### Nice to have
- Start-up & Database Locks/Cleaning
- local laws and regulations

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/US-Blue-Bell-ICON/Senior-Clinical-Trial-Manager_JR163431-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)