Clairo

eCOA Clinical Scientist

United States

Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Trials, Healthcare TechnologyIndustries

Clinical Scientist - eCOA

Employment Type: Full-time

Position Overview

The Clinical Scientist-eCOA supports the development of electronic clinical outcome assessments (eCOA’s) from a clinical perspective across therapeutic areas, in conjunction with IT Development, Operations Management, and Clinical Science. The Clinical Scientist-eCOA is responsible for ensuring the timely completion of electronic scales while adhering to quality standards and clinical validity. This individual will have experience conducting assessments as well as interacting with investigative sites and study sponsors. The incumbent will assist in ensuring the organization’s operational efficacy and excellence by working with different operational units in translating groups’ business requirements to particular software requirements and/or procedural workflows.

About Clario

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.

What We Offer (USA)

  • Competitive compensation
  • Medical, dental, and vision insurance beginning Day 1 of employment
  • Flexible work schedules
  • Attractive PTO plan
  • Engaging employee programs
  • Remote working

Education Requirements

  • Graduate degree in psychology, social work, counseling, psychiatric nursing, or related field.

Qualifications/Experience

  • Minimum 4 years’ experience administering standardized assessment tools, psychiatric symptom rating scales, and/or Neurocognition scales. Experience with structured diagnostic interviews is preferred.
  • Minimum 2 years’ experience in a clinical trial or research setting or other clinical setting is highly preferred.
  • Knowledge of scale development and clinical assessment best practices.
  • Fluent in English; bi-lingual or multi-lingual skills are preferred.
  • Basic understanding of GCP.

Essential Duties/Responsibilities

To perform this job successfully, an individual must be able to perform each essential duty and responsibility satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or ability required.

  • Provide clinical subject matter expertise in the development of eCOA’s to meet the client’s business needs.
  • Communicate and coordinate effectively with internal teams to deliver requirements for electronic form layout, interface, and validation rules/edit checks.
  • Provide support to the Business Analyst and Test teams through Clinical validation expertise to test, validate, and evaluate work completed by the eCS team.
  • Participate in team meetings and communicate regularly with remote staff and other employees.
  • Review and evaluate data collected through eCOA platforms, Independent Ratings, Independent Review, internal usability testing, surveys, and marketing research to improve functionality and clinical guidance included in eCOA’s.
  • Liaise with sponsors and scale authors, as needed.
  • Act as an external-facing clinical representative responsible for presenting eCOA batteries utilized in large, international clinical trials, to sponsors for approval/adoption.
  • Work with operational groups who test, validate, and evaluate new applications and functions, and determine clinical-related issues in services and software.
  • Identify the need for and develop, as needed, work instructions, process guidelines, and standard operating procedures. Ensure processes and procedures meet SOP/GCP requirements related to eCOA development.
  • Perform other job duties as assigned by management.
  • Ability to multi-process and delegate project tasks.
  • Advanced skills in MS Word, Excel, and Adobe.

Travel Requirements

  • Ability to travel domestically and internationally, approximately 10% of the time, including overnight stays as necessary, consistent with business needs and office location.

EEO Statement

Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Skills

eCOA
clinical outcome assessments
therapeutic areas
IT Development
Operations Management
Clinical Science
electronic scales
clinical validity
investigative sites
study sponsors
operational efficacy
software requirements
procedural workflows
standardized assessment tools
psychiatric symptom rating scales
Neurocognition scales
structured diagnostic interviews
clinical trial
research setting
scale development
clinical assessment best practices
GCP

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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