Training Operations Manager (f/m/d)

Hungary

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical ResearchIndustries

Requirements

Candidates should possess a Bachelor’s, Master’s, or Doctoral degree in a relevant subject related to the Pharmaceutical, Healthcare, or Life Science industry, which is desirable. They should have at least 2+ years of experience working in Training Operations Management or a Project Management-focused position, such as a Project Associate or Project Coordinator. Strong attention to detail, organizational, and time-management skills are required, along with the ability to prioritize tasks and manage workloads effectively. Creative and problem-solving skills are also necessary to implement internal improvement projects and meet client learning and education needs. Excellent verbal and written communication skills in English are essential, and experience within the Clinical Research, Pharmaceutical, or Healthcare industry is highly desirable.

Responsibilities

The Training Operations Manager will manage training operations projects across all Clario product/service lines, lead client meetings, develop and finalize training plans and delivery schedules, coordinate resource assignments, update project management tools, and communicate assignments to project managers. They will also coordinate timelines within the Education team, identify potential risks, escalate issues, manage the deployment of eLearning curriculums and instructor-led training via the Learning Management System, assist with training new team members, and lead/contribute to key process improvement initiatives. Furthermore, they will assist with addressing project-related issues, ensuring timely resolution to escalations, and maintaining tracking documentation to monitor progress.

Skills

Project Management

Training Operations

Client Management

Learning Management System (LMS)

eLearning Deployment

Instructor-led Training Deployment

Risk Management

Process Improvement

Resource Management

Communication

Clairo

Generates clinical evidence for trials

About Clairo

Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.

London, United KingdomHeadquarters

1972Year Founded

$29.9MTotal Funding

GROWTH_EQUITY_VCCompany Stage

Biotechnology, HealthcareIndustries

5,001-10,000Employees

Benefits

Competitive and equitable total rewards package

Physical, mental and financial health and wellness

Flexible working approach

Risks

Increased competition from AI-driven platforms like Medable may threaten Clario's market share.

The IPO filing may lead to investor pressure for rapid financial returns, affecting strategy.

AI integration from ArtiQ poses data privacy and compliance risks, especially in the EU.

Differentiation

Clario offers a comprehensive endpoint technology platform for diverse clinical trial models.

The company has nearly 50 years of experience in clinical trial technology solutions.

Clario's global presence includes 30 facilities across North America, Europe, and Asia Pacific.

Upsides

Clario's IPO aims for a valuation of over $10 billion, indicating strong market confidence.

The FDA clearance of SpiroSphere® with wireless ECG enhances Clario's clinical trial capabilities.

Clario's acquisition of ArtiQ boosts its AI capabilities in respiratory clinical trials.

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