Clairo

Clinical Project Manager

Costa Rica

Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceutical, Clinical ResearchIndustries

Requirements

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

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, and communicating information to project teams. They will perform project analysis and management by identifying critical success factors, determining needed resources, collaborating with department leaders, and understanding the project contract. The role also includes project team leadership, supporting Business Development efforts, overseeing project close-out, and performing supervisory functions such as coaching, performance evaluations, and training new hires. Furthermore, they will maintain Quality Service and Departmental Standards by adhering to SOPs, establishing departmental standards, and updating company SOPs.

Skills

Project Management
Clinical Trials
Project Planning
Financial Management
Data Collection
Team Leadership
Communication
SOPs
Training
Protocol Revision

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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