[Remote] Clinical Project Manager at Clairo

Costa Rica

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceutical, Clinical ResearchIndustries

Skills

Key technologies and capabilities for this role

Project ManagementPharmaceutical FieldCustomer Requirements GatheringStudy DocumentationBudget ManagementRevenue ForecastingScope ManagementInvoice ReconciliationRisk ManagementNegotiationProblem SolvingClient MeetingsTeam CollaborationCommunication

Questions & Answers

Common questions about this position

What experience is required for the Clinical Project Manager role?

1-4 years of experience in project management with an emphasis in the pharmaceutical field or related industry experience is required, along with knowledge of the drug development process.

What key skills are needed for this position?

Excellent organizational, interpersonal, time management, prioritization, verbal and written communication skills, working knowledge of Microsoft Office, and detail-oriented responsiveness are required.

What is the education requirement for this job?

A Bachelor’s degree and/or proven Project Management skills or experience within the industry is required, plus Clario PM Certification as applicable per Line of Business.

Is travel required for the Clinical Project Manager position?

Yes, a valid passport and ability to travel approximately 20% is required.

What does the company say about equal opportunity employment?

Clario is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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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