Clairo

Technical Implementation Manager

Costa Rica

Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Healthcare, Pharmaceuticals, Clinical ResearchIndustries

Position Overview

  • Location Type: Remote
  • Job Type: Full-time
  • Salary: Competitive salary and performance-based rewards

Clario is transforming the future of clinical trials and is seeking a Technical Implementation Manager to ensure efficient and effective delivery of solutions, aligned with project goals and client expectations.

What We Offer

  • Competitive salary and performance-based rewards
  • Comprehensive benefits supporting security, flexibility, and well-being
  • Remote work options
  • Employee engagement programs fostering growth and connection

Responsibilities

  • Lead and manage complex clinical studies independently.
  • Oversee planning and execution of multiple concurrent projects.
  • Review study documentation for clarity, consistency, and quality.
  • Collaborate with internal teams to align project requirements with our product suite.
  • Provide expert input during the specification process.
  • Identify and manage new implementation needs based on study-specific requirements.
  • Oversee post-release project activities throughout the entire project lifecycle.
  • Live issue troubleshooting & investigation.
  • Independently manage high-profile and complex studies with diverse scope (sites, products, transactions, etc.).
  • Handle the complete planning of study steps/milestones for multiple projects as assigned.
  • Review study relevant documents regarding testability, comprehensibility, plausibility, inconsistencies, requirement or quality gaps.
  • Work with internal stakeholders to understand client project requirements, providing experience and guidance on how projects can be delivered efficiently using the current product suite and help define enhancements.
  • Provide intensive consulting within the process of creating specifications (PRS, URS, DES, SRS, FS).
  • Compare study-specific requirements with existing solutions, initiate necessary new implementations and manage them with regard to requirements date and functional scope.
  • Post-release support and control until the study end.
  • Post-release issue investigation and troubleshooting.

Requirements

  • BS, BA or equivalent IT education Experience
  • 3+ years of experience in Project Management
  • Experience in Project/Product Life Cycle
  • Good understanding of Software Development Process
  • Strong communication skills and a collaborative mindset
  • Ability to read and understand documentation in English language
  • Familiarity with GCP/GMP and technical project management is a plus
  • Knowledge in programming languages/scripting, and databases are a plus

Company Information

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives. We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.

Skills

Clinical Trials
Project Management
Study Documentation
Process Specification
Troubleshooting
Stakeholder Collaboration
Study Planning
Requirement Analysis

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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