Clairo

Assistant Clinical Project Manager

Costa Rica

Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, Clinical ResearchIndustries

Requirements

Candidates should possess a Bachelor’s degree, which is preferred, and have 0-1 year of experience working with clinical trials or within a pharmaceutical environment. They should also demonstrate the ability to work effectively in a group setting and independently, adjust to changing priorities, possess excellent attention to detail, strong interpersonal and communication skills (both verbal and written), and strong organizational skills.

Responsibilities

The Assistant Clinical Project Manager will assist Clinical Project Managers with project administration by drafting project documents, reviewing and editing presentations, participating in meetings, acting as a liaison with team members, reporting study needs, assisting in maintaining project progress, monitoring data flow, responding to inquiries, verifying protocol imaging requirements, serving as an acting Project Manager, mentoring the Operations team, ensuring project timelines are met, assisting in tracking and resolving client issues, maintaining quality service, adhering to SOPs, participating in process improvement initiatives, and contributing to team efforts. They will also maintain technical knowledge through training and participate in modifying SOPs and providing recommendations to management.

Skills

Project Documentation
Presentation Review
Meeting Participation
Protocol Understanding
Cross-functional Communication
Data Monitoring
Client Communication
Microsoft Office

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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