Technical Implementation Manager

Costa Rica

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Healthcare, Pharmaceuticals, Clinical ResearchIndustries

Requirements

Candidates should possess a Bachelor’s degree in IT or a related field, or equivalent experience, and have at least 3 years of experience in project management. They should demonstrate a solid understanding of the project/product lifecycle and software development processes, along with strong communication skills and a collaborative mindset. Familiarity with Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP) is a plus, as is knowledge of programming languages and databases.

Responsibilities

As a Technical Implementation Manager, the individual will independently manage high-profile and complex clinical studies, oversee planning and execution of multiple concurrent projects, review study documentation for quality, collaborate with internal teams to align project requirements, provide expert input during the specification process, identify and manage new implementation needs, oversee post-release project activities, handle the complete planning of study steps/milestones, review study relevant documents, work with internal stakeholders to understand client requirements, provide intensive consulting during specification creation, compare study-specific requirements with existing solutions, initiate new implementations, and provide post-release support and troubleshooting.

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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