[Remote] Clinical Project Manager at Clairo

Costa Rica

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Healthcare, Clinical ResearchIndustries

Requirements

Bachelor’s degree required or commensurate experience level. Educational majors in life sciences, pharmacy, nursing, or other healthcare field highly desirable
Previous management or project experience in clinical development of investigational medications required
1-3 years clinical trials experience within a CRO or pharmaceutical

Responsibilities

Identifies project guidelines and communication needs by reviewing study requirements and response assessment criteria, collaborating with key stakeholders to develop study start-up activities and associated documents, defining project plans (timelines, milestones, limitations), establishing project reporting schedules, providing project updates to BD Director, Global Services Managing Directors, and Sponsor representative(s), and communicating timely project information to project teams, sites, and company/sponsor representative(s)
Performs project analysis and management by identifying critical project success factors for tracking, analysis, and reporting, determining needed resources and communicating to departmental managers, collaborating with department leaders for training, performing financial tasks (monthly billing, forecasting, project scope reviews/amendments, pass-through cost management), understanding project contract for revenue reporting, understanding SOPs and working with QA for deviations, training project team on SOPs, and communicating protocol clarifications/revisions
Coordinates site management of data collection with internal and external teams
Provides project team leadership by leading by example with professional conduct, developing/delivering team training, establishing performance expectations, providing input on team member performance to managers, analyzing team performance, and collaborating on coaching/mentoring
Supports Business Development efforts by collaborating with BD Director on capabilities calls/meetings, attending professional meetings as Company representative, and delivering Investigator Meeting presentations
Oversees project close out by assisting with submission activities and initiating/overseeing close out activities to completion
Performs supervisory functions (if applicable) by communicating job expectations, planning/monitoring/appraising results, coaching/counseling/disciplining staff, enforcing systems/policies/procedures, approving time sheets/time off/overtime, performing evaluations, coordinating interviews/hiring, and training new hires
Maintains Quality Service and Departmental Standards by adhering to SOPs, establishing/enforcing departmental standards, and reviewing/updating company SOPs
Contributes to team effort by exploring new opportunities to add value, helping others accomplish results, and performing other duties as assigned
Maintains Technical Knowledge by attending/participating in company-sponsored training

Skills

Project Management

Clinical Study Management

Stakeholder Collaboration

Timeline Management

Financial Forecasting

Billing

SOP Compliance

QA Collaboration

Team Leadership

Site Management

Data Collection Coordination

Protocol Management

Risk Analysis

Resource Allocation

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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