[Remote] eCOA Clinical Scientist at Clairo

United States

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Not SpecifiedCompensation

N/AExperience Level

N/AJob Type

Not SpecifiedVisa

N/AIndustries

Requirements

Graduate degree in psychology, social work, counseling, psychiatric nursing, or related field
Minimum 4 years of experience administering standardized assessment tools, psychiatric symptom rating scales, and/or neurocognition scales; experience with structured diagnostic interviews preferred
Minimum 2 years of experience in a clinical trial, research, or clinical setting
Knowledge of scale development and clinical assessment best practices
Fluent in English; bilingual or multilingual skills preferred
Basic understanding of Good Clinical Practice (GCP)
Advanced skills in MS Word, Excel, and Adobe
Ability to travel domestically and internationally up to 10%, including overnight stays
Based in or able to work from the United States (remote/hybrid)

Responsibilities

Provide clinical subject matter expertise in the development of eCOAs to meet client needs
Communicate and coordinate with internal teams to deliver requirements for electronic form layout, interface, and validation rules/edit checks
Support Business Analyst and Test teams through clinical validation expertise to test, validate, and evaluate work completed by the eCOA team
Review and evaluate data collected through eCOA platforms, Independent Ratings, usability testing, surveys, and marketing research to improve functionality and clinical guidance
Liaise with sponsors and scale authors as needed
Present eCOA batteries used in large, international clinical trials to sponsors for approval/adoption
Collaborate with operational groups to identify and resolve clinical-related issues in services and software
Develop work instructions, process guidelines, and SOPs to ensure compliance with SOP/GCP requirements related to eCOA development
Participate in team meetings and maintain regular communication with remote staff
Perform other duties as assigned by management

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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