Project Specialist Scales Management

Costa Rica

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Not SpecifiedCompensation

Entry Level & New Grad, Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, Biotechnology, PharmaceuticalsIndustries

Requirements

Candidates should possess a Bachelor's degree in a related field and have 0-2 years of project coordination experience. A proven track record of adhering to timelines and being a productive cross-functional team member is necessary. HTML and foreign language experience are preferred.

Responsibilities

The Project Specialist will assist the Translations team with daily tasks, including screenshot development, proofreading, and quality control checks on deliverables. They will troubleshoot errors, participate in client-facing meetings under mentorship, and schedule/scope translation projects with support. Responsibilities also include managing translation study budgets, overseeing translation vendor deliverables and timelines, and ensuring compliance with Good Clinical Practices. The role involves providing instrument and library support, fixing translation defects during software testing, educating others on the translations process, and evaluating processes for continuous improvement.

Skills

Project Management

Quality Control

Translation

Proofreading

Regulatory Compliance

Good Clinical Practices

Vendor Management

Clinical Trials

Software Testing

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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