Clairo

Project Coordinator, Respiratory

Costa Rica

Not SpecifiedCompensation
Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceutical, Clinical TrialsIndustries

Job Description

Position Overview

Clario is a 50+ year old company that delivers industry-leading clinical trial endpoint technology solutions. The future of clinical trials is vibrant, with new technologies revolutionizing what’s possible. From new trial modes to faster and integrated evidence and findings, our innovative clinical trial solutions mean we can unlock better evidence.

Employment Type

Full time

Salary

Not specified

Location Type

Not specified

What We Offer

  • Competitive compensation
  • Private health insurance
  • Engaging employee programs
  • Flexible work schedules
  • Attractive PTO plan
  • Flex workspace

Responsibilities

  • Assist Project Management personnel with various tasks throughout the study lifecycle.
  • Assist with the Planning and Setup, Monitoring, and Closeout Phases of study management, which may include:
    • Database setup.
    • Study documentation development.
    • Equipment distribution/tracking.
    • Report creation/distribution.
    • Archival of study documentation.
  • Coordinate Project Assurance meetings and assist with compiling meeting minutes and action items.
  • Support financial components of study management, including:
    • Assistance with documentation/database updates due to scope changes.
    • Follow-up related to invoice reconciliations.
    • Preparation of reports in support of study forecasting activities.
  • Facilitate issue management by documenting and tracking progress to ensure timely resolution to customer escalations.

Other Duties and Responsibilities

  • Ensure compliance with timely training completion/documentation.
  • Respond to customer inquiries and participate in customer calls/meetings upon Project Manager’s request.
  • Take the lead in managing various aspects of a project as requested.
  • Other related projects and tasks as assigned.

Requirements

  • Education: Bachelor Degree preferred.
  • Experience: At least 1-3+ years of experience in the pharmaceutical field (or related industry experience).
  • Knowledge:
    • Knowledge of the drug development process.
  • Skills:
    • Good organizational, interpersonal, time management, and prioritization skills.
    • Excellent verbal and written communication skills, including the ability to communicate effectively in English.
    • Detail-oriented and responsive to inquiries and requests.
    • Working knowledge of Microsoft Office products.

EEO Statement

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

Skills

Project Management
Database Setup
Study Documentation
Equipment Tracking
Report Creation
Meeting Coordination
Invoice Reconciliation
Issue Management
Customer Inquiries
Pharmaceutical Industry
Drug Development Process
Organizational Skills
Interpersonal Skills
Time Management
Prioritization Skills

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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