[Remote] Project Manager at Clairo

United States

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Not SpecifiedCompensation

N/AExperience Level

N/AJob Type

Not SpecifiedVisa

N/AIndustries

Requirements

Bachelor’s degree and/or proven Project Management skills or experience within the industry
1-4 years of experience in project management with an emphasis in the pharmaceutical field (or related industry experience)
Software Development Life Cycle (SDLC) experience
Knowledge of the drug development process
Valid passport and ability to travel approximately 20%

Responsibilities

Lead the Planning and Setup, Monitoring, and Closeout phases of study management
Gather customer requirements and relay to internal teams
Develop study documentation
Distribute/track equipment
Create/distribute reports
Archive study data and documentation
Monitor study timelines and manage the financial components of each program/study
Identify potential study risks and mitigations and escalate as appropriate
Manage internal/external negotiations and promote collaboration
Apply problem solving strategies to address customer issues and maintain issue tracking documentation
Ensure compliance with timely training completion/documentation
Present study services at Investigator Meetings or site initiation meetings as needed
Attend client meetings with Business Development and/or Operational teams
Assist with training new members of the Project Management team
Perform other duties, assignments, or special projects as time and/or circumstances necessitate

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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