Lead Data Coordinator

Bengaluru, Karnataka, India

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Healthcare, Clinical ResearchIndustries

Requirements

Candidates should possess a minimum of 5 years of experience in a data coordination role, with a strong understanding of data management principles and procedures. The role requires familiarity with ECG, Holter, and Flashcard/Transmittal Form data, along with experience investigating and resolving data queries. Prior experience with EXPeRT and Data Cleaning Application is preferred.

Responsibilities

As a Lead Data Coordinator, you will monitor daily workflow, direct team assignments, and ensure all team tasks are completed daily. You will investigate and issue queries to sites/sponsors, enter resolutions, maintain data coordination files, perform self-evident corrections, and revise data revision request forms. Additionally, you will attend project assurance meetings, assist with data entry and scanning, train new staff, conduct performance evaluations, prepare client activity metrics, and maintain daily communication between shifts, while also overseeing employee productivity and quality metrics.

Skills

Data Coordination

SOP Compliance

Protocol Compliance

Training

Quality Metrics

Workflow Management

Data Clarification

Data Entry

Scanning

Barcoding

Team Leadership

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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