Translations Project Manager I

India

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Life Sciences, Clinical Trials, TranslationsIndustries

Requirements

Candidates must possess a Bachelor's degree in a related field and have 2-3 years of project management experience. Strong attention to detail, proofreading skills, and the ability to meet deadlines and collaborate cross-functionally are essential. Experience in regulated environments, particularly in the life sciences or translations industry, and familiarity with software development processes are preferred.

Responsibilities

The Translations Project Manager will manage all translation-related tasks for assigned studies, including coordinating internal and external resources. This includes leading screenshot development and proofreading, managing translation vendors, project budgets, and timelines, and facilitating client-facing communication. The role also involves providing subject matter expertise on linguistic validation and regulatory submissions, troubleshooting technical issues related to translation builds, and training vendors. Additionally, the project manager will support continuous improvement efforts and mentor new team members.

Skills

Project Management

Translation Management

Linguistic Validation

Quality Control

Vendor Management

Budget Management

Timeline Management

Client Communication

Regulatory Affairs

Software Development Processes

Proofreading

Attention to Detail

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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