Clairo

Clinical Project Manager

Pennsylvania, United States

Clairo Logo
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, Clinical Research, HealthcareIndustries

Requirements

Candidates should possess a Bachelor’s degree, or commensurate experience, in life sciences, pharmacy, nursing, or another healthcare field, and previous management or project experience in clinical development of investigational medications is required. 1-3 years of clinical trials experience is preferred.

Responsibilities

The Clinical Project Manager will identify project guidelines and communication needs by reviewing study requirements and collaborating with stakeholders to develop study start-up activities and documents, establishing project plans and reporting schedules, providing project updates, performing project analysis and management, determining needed resources, collaborating with department leaders, coordinating site management, leading project teams, supporting Business Development efforts, overseeing project close-out activities, performing supervisory functions including coaching and performance evaluations, maintaining Quality Service and Departmental Standards by adhering to SOPs, and maintaining technical knowledge through training. They will also contribute to team efforts and perform other duties as assigned.

Skills

Project Management
Study Start-up
Study Requirements
Communication
Project Planning
Reporting
Stakeholder Collaboration
Resource Allocation
Financial Management
SOPs
Quality Assurance
Data Management
Team Leadership
Training

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.

Key Metrics

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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