Clairo

Data Coordinator

Costa Rica

Not SpecifiedCompensation
Entry Level & New Grad, Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Trials Technology, HealthcareIndustries

Data Coordinator

Position Overview

The Data Coordinator focuses on initiating, investigating, and resolving queries based on discrepancies identified by the database in accordance with Clario’s SOPs and SWIs. They are also responsible for maintaining organized study documentation throughout the lifecycle of a study.

Company Information

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

  • Competitive compensation
  • Private health insurance
  • Engaging employee programs
  • Flexible work schedules
  • Attractive PTO plan
  • Flex workspace

Essential Duties and Responsibilities

  • Support department workflow by taking action on discrepant data through investigation and issuance of queries to sites/sponsors to verify/obtain demographic and visit information on source data in accordance with departmental SOPs and SWIs.
  • Investigate and enter resolutions and/or revisions received across operational systems.
  • Process source data across operational systems.
  • File source documents once workflow is complete.
  • Maintain departmental metrics in accordance with goal plan.
  • Participate in required training programs.
  • Report any equipment and/or system problems.
  • Maintain accurate and complete Data Coordination files as defined by the department’s SOPs.
  • Archive closed studies upon notification of study lock within the requested timeframe.
  • Assist as requested with data reconciliation activities for your studies, ensuring that database updates are completed within the Sponsor-requested timelines.

Other Duties and Responsibilities

  • Attend Project Assurance meetings and outline feedback to Data Coordination.
  • Support the training of new temporary employees.

Qualifications and Skills Needed

  • Education: BS or BA degree in life sciences or related field preferred.
  • Experience: 2 years of company or related data processing experience.
  • Skills:
    • Good organizational, problem-solving, and communication skills.
    • Demonstrated computer proficiency in MS Word, Excel, and Outlook.
    • Detail-oriented with good proofreading skills.
    • Proficient data entry/typing skills.

Employment Type

Full time

Location Type

Information not specified

Salary

Information not specified


The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. Clario reserves the right to amend or change this job description to meet the needs of Clario. This job description and any attachments do not constitute or represent a contract. The Department Head has the discretion to hire personnel with a combination of experience and education, which may vary from the above-listed qualifications.

Skills

Data Management
Database
SOPs
SWIs
Clinical Trials
Data Reconciliation
Documentation
Problem-Solving
Communication

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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